Dr Pasupathy Arumugam
Consultant Pathologist | DNA Labs India Medical Team
Dr Pasupathy Arumugam
Consultant Pathologist
MBBS, MD (Pathology)
🏅 Reg. No: 21521 ⏳ 15+ years experience
Credentials
MBBS, MD (Pathology)
Recognized By
Tamil Nadu Medical Council
Registry Number
21521
Experience
15+ years
Tests Medically Reviewed by Dr Pasupathy Arumugam
- 1B-Cell Rearrangement Detection Test
- 2Chlamydia IgG Antibody Panel Test
- 3Alkaline Phosphatase Bone-Specific; BSAP Test
- 4Thrombotic Risk Screen Test
- 5(CA) Cyfra 21-1 Lung Cancer Marker Test
- 8Breast Cancer ER PR HER-2 Ki-67
- 15Epstein-Barr Virus Early RNA (EBER-ISH) In-Situ-Hybridization Test
- 17Immunohistochemistry MUC4 Test
- 22FISH - Equivocal HER2 (ERBB2) Test
- 28Immunohistochemistry MUC5AC Test
- 29Leucocyte Alkaline Phosphatase Score (LAP Score) Test
- 31OncoPro NCCN Lung Cancer Panel with PD-L1 Test
- 32OncoPro Colorectal Cancer Screen - Circulating Tumor Cells Test
- 33OncoPro Pan Cancer Monitor Test
- 34OncoPro Prostate Cancer Screen Test
- 42T-Cell Gene Rearrangement Mutation Detection Test
- 43OncoPro PD-L1 Circulating Tumor Cells Test
- 455-HIAA (5-Hydroxy Indole Acetic Acid) Random Urine Test
- 465-HIAA (5-Hydroxy Indole Acetic Acid) 24 Hour Urine Test
- 58Acute Lymphoblastic Leukemia (ALL) Cytogenetics Panel Test
- 60Activated Protein C-Resistance (APCR) Test
- 61ADAMTS13 Activity Test
- 62Adenovirus Qualitative PCR Test
- 69AFP (Alpha Fetoprotein): Tumor Marker Test
- 73Aldosterone / Renin Direct Ratio Plasma Test
- 74Alcohol (Ethanol) Screen Serum Test
- 76Alkaline Phosphatase (ALP) Isoenzymes Test
- 79Allergy Phadiatop Adult Test
- 87Alpha-2-Macroglobulin Test
- 92Amenorrhoea / Andrology Screen Test
- 97Amino Acids Qualitative Urine & Plasma Test
- 104AML Categorization PCR Test
- 105Liver Ammonia Blood Test
- 115ANCA (Anti Neutrophil Cytoplasmic Antibodies) Positive Reflex to ANCA-MPO & ANCA-PR3 Test
- 124Anemia of Chronic Disease (ACD) Panel Test
- 129Anemia Panel Basic Test
- 130Anti A Titre IgM Test
- 135Anti B Titre IgG Test
- 137Anti-ds DNA Antibody EIA Test
- 154Anti Thyroglobulin Antibody (Anti Tg) Test
- 158Anti-NMO (Neuromyelitis Optica) Antibody / Aquaporin 4 Test
- 165Antithrombin Activity Functional Test
- 167Arthritis Panel 2 Test
- 168Arthritis Panel Basic Test
- 192Beta 2 Glycoprotein 1 Panel IgG, IgM & IgA Test
- 193Bacterial Vaginosis (BV) Rapid Assay Test
- 194Beta-2-Microglobulin 24 Hour Urine Test
- 195Beta-2-Microglobulin Serum Test
- 196BCR-ABL Quantitative MRD Monitor Test
- 197Bile Acids Total Serum Test
- 204BCR-ABL Gene Rearrangement PCR Quantitative Test
- 206Biotinidase Activity Quantitative Blood Test
- 207BK Virus PCR Qualitative Test
- 212Blood Gas Analysis Venous Test
- 215Bone Marrow Examination Panel 1 Test
- 216BOH (Bad Obstetric History) Advanced Panel Test
- 224BRAF Mutation Analysis Test
- 225Brucella Antibodies Panel IgG & IgM Test
- 226Breast Metastatic Marker Test
- 237C7 Complement Test
- 241CA 15.3 Breast Cancer Marker Test
- 242CA 19.9 Pancreatic Cancer Marker Test
- 243CA 125 Ovarian Cancer Marker Test
- 244CA 72.4 Gastric Cancer Marker Test
- 245CA 27.29 Breast Cancer Marker Test
- 247CA 27.29 & CA 15.3 Breast Cancer Markers Panel Test
- 248Cadmium Blood Test
- 251CAN Assist Breast Test
- 255Cancer Targeted Gene Panel CNS Tumor Test
- 257Cancer Targeted Gene Panel: Gastrointestinal Stromal Tumor (GIST) Test
- 260Cancer Targeted Gene Panel: Lung with PDL-1 (DAKO) Test
- 263Cancer Targeted Gene Panel: Colon / Colorectal Test
- 265Cannabinoids (Delta-9-THC Metabolites) / Marijuana Confirmation Urine Test
- 276Catecholamines & VMA 24 Hour Urine Test
- 277Carotene Test
- 278CEBPA Mutation Detection Test
- 281CEA Carcino Embryonic Antigen Test
- 282Ceruloplasmin Test
- 283Celiac Disease Screening Panel Test
- 286Catecholamines Fractionated Random Urine Test
- 290Chimerism Pre-Engraftment Test
- 291Chimerism Split Cell Analysis - B Cell (CD19) Test
- 293Chimerism Split Cell Analysis - Myeloid Cell (CD15) Test
- 296Chimerism Split Cell Analysis - T Cell (CD3) Test
- 300Chromium Blood Test
- 304Chromosome Analysis (Karyotype) Blood Test
- 307Chromogranin A CGA Test
- 309Chromosome Analysis Solid Tumor Test
- 318Chronic Lymphocytic Leukemia (CLL) Mutations Detection Comprehensive Panel Test
- 319Chronic Lymphocytic Leukemia (CLL) Mutations Detection Panel 1 Test
- 320Chronic Fatigue Syndrome Test
- 334Coagulation Profile 1 Test
- 345Complete Body Panel Test
- 352Copper Serum Test
- 355Cortisol Suppression by Dexamethasone Overnight High Dose Test
- 360Coxsackie Antibodies IgG & IgM Panel Test
- 369C-Peptide 24 Hour Urine Test
- 391Culture AFB (Mycobacterium) Rapid Test
- 396Culture Diphtheria Test
- 416Culture Malassezia Test
- 424Cultured AFB Antitubercular DST Capreomycin Test
- 428Cultured AFB Other Than Tuberculosis (MOTT) DST for Slow Growers Test
- 436Cultured AFB Antitubercular DST PAS Test
- 452Cultured AFB Antitubercular DST Streptomycin Test
- 455Cyclosporine A Test
- 459Cytology Fine Needle Aspiration FNAC Test
- 462Cytomegalovirus (CMV) Antibody IgG Test
- 465Cytology (Pap Smear) Genital Female Liquid Based Test
- 466Cytomegalovirus (CMV) Antibody IgM Test
- 470Cytomegalovirus (CMV) IgG Advantage Test
- 473Dengue Fever IgG Antibody EIA Test
- 479Dengue Fever IgM Antibody EIA Test
- 483Des-Gamma Carboxy Prothrombin (DCP)/PIVKA II Serum Test
- 485Desipramine Test
- 487Desmoglein (DSG) 1 & 3 Antibody Test
- 491Desmoglein (DSG) 1 and 3 Antibody in Dilution/End Point Titre Test
- 499Diabetes Panel 2 Test
- 508Electron Microscopy (TEM) Test
- 510EGFR Mutational Analysis Test
- 512Enhanced Liver Fibrosis (ELF) Panel Test
- 518Epidermal (Pemphigus) Antibody IFA in Dilutions Test
- 520Episodic Ataxia Comprehensive Profile Hotspot Test
- 527Epidermal (Pemphigus) Antibody IFA Test
- 530Erythropoietin (EPO) Test
- 536Extractable Nuclear Antigens (ENA) / Anti Nuclear Antibodies (ANA) Quantitative Profile Test
- 538Factor V Functional Test
- 541Executive Officers Panel Test
- 554Fibrinogen Degradation Products (FDP) Blood Test
- 557Fibroblast Growth Factor (FGF2) Test
- 560FISH - 1p & 19q Codeletion Test
- 562FISH - 14q32.3 or LSI IGH Gene Breakapart Test
- 565FISH - 22q Deletion or LSI Di George / VCFS Test
- 566FISH - Aggressive Lymphoma Panel Test
- 567FISH - 17p (TP53) Deletion Test
- 568FISH - ALK-1 Breakapart Rearrangement Test
- 573FISH - Amnio Two Probes: Trisomy 13 & 21 Test
- 580FISH - Eosinophilic Leukemia Panel Test
- 582FISH for HER-2 Neu
- 584FISH - Multiple Myeloma with Positive Selection of CD138 Cells Test
- 585FISH - MDM2 (12q15) Gene Amplification Test
- 587FISH - MYCN Amplification Test
- 589FISH - NTRK 2 Gene Rearrangement Assay Test
- 592FISH - NTRK 1 Gene Rearrangement Assay Test
- 593FISH - PDGFR Alpha (4q12) Gene Rearrangement Test
- 595FISH - PDGFR Beta (5q33) Gene Rearrangement Test
- 603FISH - Synovial Sarcoma (SS18 / SYT) 18q11.2 Gene Rearrangement Test
- 604FISH - t(11;14) or LSI IGH/CCND1 Test
- 606FISH - t(15;17) or LSI PML/RARA Test
- 607FISH - ROS1 (6q22) Rearrangement Test
- 612Flecainide Test
- 614FISH - NTRK 1, 2 & 3 Gene Panel Test
- 615FLT3 Gene Mutation Test
- 617Folate (Folic Acid) Serum Test
- 621Folate (Folic Acid) RBC Test
- 625FSH & LH Test
- 628FSH (Follicle Stimulating Hormone) Test
- 629G-6-PD Quantitative Test
- 633Galactomannan (Aspergillus Antigen) Serum Test
- 634Galactose Quantitative Plasma Test
- 641Ganglioside GD1b Antibody IgG Test
- 645Ganglioside GQ1B Antibody IgG Test
- 647Ganglioside GD1b Antibody IgM Test
- 650Genetic Mapping for Cardiovascular Disorders Test
- 655GeneXpert MTB Combo.com Test
- 657Genetic Mapping for Oncology / Cancer Test
- 658GeneXpert MTB.com Test
- 662Gliadin Deamidated Antibodies Panel IgA & IgG Test
- 665Glioma Prognostic Panel Test
- 666Germ Cell Tumor Panel Test
- 670Glucose Estimation 2.5 Hours Test
- 683H3N2 & Influenza B Qualitative PCR Test
- 684Haloperidol Test
- 685HAM Test Paroxysmal Nocturnal Hemoglobinuria (PNH) Screening Test
- 688HE4 Human Epididymis Protein 4 Test
- 689Heart Screen Test
- 690Heavy Metal Screen Test
- 691Hair Transplant Panel A Test
- 695Helicobacter Pylori IgG Test
- 700Hemophilia Panel Test
- 701Hemophilia A Carrier Detection Test
- 706Hepatitis B Immunity Screen Test
- 709Heparin Anti Xa Test
- 711Hepatitis B Monitoring Panel Test
- 716Hepatitis B Virus Genotyping Drug Resistance & Quantitative PCR Test
- 720Hepatitis C Monitoring Panel Test
- 723Hepatitis C Viral RNA (HCV RNA) Quantitative Real Time PCR Test
- 730Hepatitis E Antibody (Anti-HEV) IgG Test
- 733Hepatocellular Carcinoma (HCC) Panel Test
- 740Herpes Simplex Virus (HSV) 2 Antibodies Panel IgG & IgM Serum Test
- 744Herpes Simplex Virus (HSV) 2 IgG Serum Test
- 751Histo/ IHC/Cyto Digitization of Slides 11 to 20 Slides Test
- 753Histo/ IHC/Cyto Digitization of Slides Up to 5 Slides Test
- 755Histone Antibodies Test
- 759Histopathology Biopsy: Bone Test
- 760Histopathology Kidney Biopsy Panel 1 Test
- 763Histopathology Biopsy: Large Complex / Cancer Specimen Test
- 764Histopathology Liver Biopsy Panel Test
- 767Histopathology Skin Biopsy Panel Test
- 768Human Immunodeficiency Virus 1 & 2 Antibodies Screening Test
- 774Human Immunodeficiency Virus -2 Detection PCR Test
- 780HLA C Locus Typing: Any Antigen Test
- 794HLA - Panel Reactive IgG Antibodies (PRA) Class I Quantitative Test
- 796HLA - DR3 (DRB1*03) Test
- 806HLA DNA Typing for Bone Marrow Transplant: 10 Antigens PCR Test
- 810HLA DNA Typing for Bone Marrow Transplant: 6 Antigens Luminex Test
- 815HLA Pre-Transplant Workup Non Sensitized Recipient Panel 1 Test
- 818HLA Pre-Transplant Workup Sensitized Recipient Panel 3 Test
- 820HLA Pre-Transplant Workup Panel 2 Test
- 826HLA Single Antigen Bead Assay for Class II IgG Antibodies DSA-SAB Class II Test
- 827Histopathology Biopsy: Large Specimen Test
- 834HTLV - I / II Antibody Confirmation Test
- 835Human Herpesvirus 6 (HHV6) Qualitative PCR Test
- 836Homovanillic Acid (HVA) Random Urine Test
- 839Hypercalcemia Panel 1 Test
- 843Homovanillic Acid (HVA) 24 Hour Urine Test
- 846Hypogonadism Panel Females Test
- 849Hypothyroidism / Hashimoto's Disease Panel Test
- 855Imatinib Resistance Mutation Analysis IRMA Test
- 856IgVH Hypermuation Analysis Confirmatory Test
- 867Immune Deficiency Panel 5 Test
- 868Immune Deficiency Panel 4 CD4 Counts Test
- 873Immunoglobulin IgG Subclasses Test
- 874Immunoglobulin IgD Serum Test
- 876Immunofixation Electrophoresis (IFE) 24 Hour Urine Test
- 878Immunoglobulin IgG Serum Test
- 879Immunohistochemistry CD103 Test
- 882Immunohistochemistry Beta-Catenin Test
- 883Immunohistochemistry CD163 Test
- 884Immunohistochemistry FLI-1 Test
- 887Immunohistochemistry MOC31 Test
- 888Immunohistochemistry Digital Breast Cancer Panel 4 Test
- 889Immunohistochemistry CD57 Test
- 890Immunohistochemistry Comprehensive Panel Test
- 891Immunohistochemistry Glycophorin A (GPA) Test
- 895Immunohistochemistry MUC4 Test
- 897Immunohistochemistry Carbonic Anhydrase-9 (CA-9) Test
- 898Immunohistochemistry HBME-1 Test
- 899Immunohistochemistry Cathepsin D Test
- 900Immunohistochemistry LIN-28 Test
- 901Immunohistochemistry Digital Breast Cancer Panel 1 Test
- 902Immunohistochemistry H3K27M / H3K27me3 Test
- 904Immunohistochemistry BRAF V600E Test
- 905Immunohistochemistry HSP70 Test
- 906Immunohistochemistry PD-L1 22C3 Test
- 907Immunohistochemistry ALKD5F3 Test
- 908Immunohistochemistry AMACR Test
- 911Immunohistochemistry BCL-6 Test
- 912Immunohistochemistry Calcitonin Test
- 913Immunohistochemistry Myeloperoxidase (MPO) Test
- 914Immunohistochemistry CD10 Test
- 915Immunohistochemistry Caldesmon Test
- 916Immunohistochemistry CD117 Test
- 917Immunohistochemistry CD15 Test
- 918Immunohistochemistry CD21 Test
- 919Immunohistochemistry CD138 Test
- 920Immunohistochemistry CD1a Test
- 921Immunohistochemistry CD35 Test
- 922Immunohistochemistry CD3 Test
- 923Immunohistochemistry CD23 Test
- 924Immunohistochemistry CD31 Test
- 925Immunohistochemistry CD79a Test
- 926Immunohistochemistry CD30 Test
- 927Immunohistochemistry CD99 (MIC-2) Test
- 928Immunohistochemistry CDX-2 Test
- 929Immunohistochemistry CEA (Carcinoembryonic Antigen) Test
- 930Immunohistochemistry Cyclin-D1 Test
- 931Immunohistochemistry CK-5/6 Test
- 932Immunohistochemistry CD5 Test
- 934Immunohistochemistry Cytomegalovirus (CMV) Test
- 935Immunohistochemistry Glial Fibrillary Acidic Protein (GFAP) Test
- 936Immunohistochemistry Epidermal Growth Factor Receptor (EGFR) Test
- 938Immunohistochemistry Human Chorionic Gonadotropin (HCG) Test
- 939Immunohistochemistry DOG-1 Test
- 941Immunohistochemistry Hepatocyte Specific Antigen (HSA) Test
- 942Immunohistochemistry Lambda Light Chains Test
- 943Immunohistochemistry HER-2 / ERBB2 (Breast) Test
- 944Immunohistochemistry HMB-45 Test
- 945Immunohistochemistry Growth Hormone (GH) Test
- 946Immunohistochemistry Myogenin Test
- 947Immunohistochemistry Neurofilament Polypeptide Test
- 948Immunohistochemistry Neuron Specific Enolase (NSE) Test
- 949Immunohistochemistry p53 Test
- 950Immunohistochemistry IgG (Polyclonal) Test
- 951Immunohistochemistry p63 Test
- 952Immunohistochemistry AFP (Alpha Feto Protein) Test
- 953Immunohistochemistry ROS1 IHC Test
- 954Immunohistochemistry Prolactin Test
- 955Immunohistochemistry ACTH Test
- 956Immunohistochemistry Prostate Specific Antigen (PSA) Test
- 957Immunohistochemistry SATB2 Test
- 958Immunohistochemistry S100 Test
- 960Immunohistochemistry Any 3 Markers Test
- 961Immunohistochemistry Any 5 Markers Without Interpretation Test
- 962Immunohistochemistry Any 3 Markers Without Interpretation Test
- 963Immunohistochemistry ATRX Test
- 964Immunohistochemistry Any 5 Markers Test
- 965Immunohistochemistry Arginase-1 Test
- 967Immunohistochemistry BCL-2 Test
- 968Immunohistochemistry CD19 Test
- 969Immunohistochemistry Calretinin Test
- 970Immunohistochemistry CD34 Test
- 971Immunohistochemistry Bladder vs Prostate Carcinoma Panel Test
- 972Immunohistochemistry CD43 Test
- 973Immunohistochemistry CD20 Test
- 974Immunohistochemistry CD61 Test
- 975Immunohistochemistry CD4 Test
- 976Immunohistochemistry CD68 Test
- 977Immunohistochemistry CD45 (LCA) Test
- 978Immunohistochemistry CD57 Test
- 979Immunohistochemistry CD56 Test
- 980Immunohistochemistry CD45 Ro (PAN T) Test
- 981Immunohistochemistry CD8 Test
- 982Immunohistochemistry Cytokeratin-7 (CK-7) Test
- 983Immunohistochemistry C-MYC Test
- 984Immunohistochemistry CDK-4 Test
- 985Immunohistochemistry Cytokeratin (Pancytokeratin) Test
- 986Immunohistochemistry CD7 Test
- 987Immunohistochemistry D2-40 (Podoplanin) Test
- 988Immunohistochemistry Desmin Test
- 989Immunohistochemistry Chromogranin-A (CGA) Test
- 990Immunohistochemistry Estrogen Receptor (ER) Test
- 991Immunohistochemistry Follicle Stimulating Hormone (FSH) Test
- 993Immunohistochemistry Cytokeratin-19 (CK-19) Test
- 994Immunohistochemistry E-Cadherin (ECAD) Test
- 995Immunohistochemistry Galectin-3 Test
- 996Immunohistochemistry GATA-3 Test
- 997Immunohistochemistry Germ Cell Tumour Panel Test
- 998Immunohistochemistry Glycophorin - A Test
- 999Immunohistochemistry Glypican-3 (GPC3) Test
- 1000Immunohistochemistry Glutamine Synthetase Test
- 1001Immunohistochemistry IgG4 Test
- 1002Immunohistochemistry Inhibin Test
- 1003Immunohistochemistry HHV-8 Test
- 1005Immunohistochemistry Isocitrate Dehydrogenase (IDH-1) Test
- 1006Immunohistochemistry Langerin Test
- 1007Immunohistochemistry Ki-67 Test
- 1008Immunohistochemistry INI-1 Test
- 1009Immunohistochemistry Kappa Light Chains Test
- 1010Immunohistochemistry LMO2 Test
- 1011Immunohistochemistry LECT2 Test
- 1012Immunohistochemistry LIN28 Test
- 1013Immunohistochemistry LMW-CK Test
- 1014Immunohistochemistry Lung Non-Small Cell Carcinoma (NSCC) Panel Test
- 1015Immunohistochemistry Luteinizing Hormone (LH) Test
- 1016Immunohistochemistry Neuroendocrine Tumor Panel Test
- 1017Immunohistochemistry OLIG2 Test
- 1018Immunohistochemistry P40 Test
- 1019Immunohistochemistry MUM1 Test
- 1020Immunohistochemistry OCT-2 Test
- 1023Immunohistochemistry PAX-5 Test
- 1024Immunohistochemistry PAX-8 Test
- 1026Immunohistochemistry P57 Test
- 1027Immunohistochemistry Perforin Test
- 1028Immunohistochemistry Pituitary Adenoma Panel Test
- 1029Immunohistochemistry PD-1 Test
- 1033Immunohistochemistry Prostate Benign vs Malignant Panel Test
- 1034Immunohistochemistry PLAP Test
- 1035Immunohistochemistry Single Marker Without Interpretation Test
- 1036Immunohistochemistry PS2 Test
- 1037Immunohistochemistry SOX-10 Test
- 1038Immunohistochemistry Serum Associated Amyloid (SAA) Test
- 1039Immunohistochemistry STAT6 Test
- 1040Immunohistochemistry SOX-11 Test
- 1041Immunohistochemistry SALL 4 Test
- 1042Immunohistochemistry STAT-6 Test
- 1043Immunohistochemistry Synaptophysin Test
- 1044Immunohistochemistry PD-L1 SP263 (Ventana) Test
- 1046Immunohistochemistry TFE 3 Test
- 1047Immunohistochemistry Thyroglobulin (TG) Test
- 1049Immunohistochemistry TLE1 (1F5) Test
- 1050Immunohistochemistry TTF-1 (Thyroid Transcription Factor-1) Test
- 1051Immunohistochemistry Uroplakin-III Test
- 1052Immunohistochemistry NKX 3.1 Test
- 1053Immunophenotyping by Flow Cytometry CD117 Test
- 1054Immunohistochemistry Vimentin Test
- 1055Immunohistochemistry WT-1 Test
- 1056Immunophenotyping by Flow Cytometry CD16 + 56 Test
- 1057Immunohistochemistry Thyroid Carcinoma Panel Test
- 1058Immunophenotyping by Flow Cytometry FMC-7 Test
- 1059Immunophenotyping by Flow Cytometry CD64 Test
- 1060Immunophenotyping by Flow Cytometry CD25 Test
- 1061Immunophenotyping by Flow Cytometry CD11c Test
- 1062Immunophenotyping by Flow Cytometry CD103 Test
- 1063Immunophenotyping by Flow Cytometry CD123 Test
- 1064Immunophenotyping by Flow Cytometry CD13 Test
- 1065Immunophenotyping by Flow Cytometry CD138 Test
- 1066Immunophenotyping by Flow Cytometry CD15 Test
- 1067Immunophenotyping by Flow Cytometry CD1a Test
- 1068Immunophenotyping by Flow Cytometry CD19 Test
- 1069Immunophenotyping by Flow Cytometry CD34 Test
- 1070Immunophenotyping by Flow Cytometry CD3 Test
- 1071Immunophenotyping by Flow Cytometry CD23 Test
- 1072Immunophenotyping by Flow Cytometry CD33 Test
- 1074Immunophenotyping by Flow Cytometry CD36 Test
- 1075Immunophenotyping by Flow Cytometry CD34 (Stem Cell) Enumeration Test
- 1076Immunophenotyping by Flow Cytometry CD45 Test
- 1078Immunophenotyping by Flow Cytometry CD10 (CALLA) Test
- 1079Immunophenotyping by Flow Cytometry CD41a Test
- 1080Immunophenotyping by Flow Cytometry CD49d Test
- 1081Immunophenotyping by Flow Cytometry CD5 Test
- 1082Immunophenotyping by Flow Cytometry CD79b Test
- 1084Immunophenotyping by Flow Cytometry HLA DR Test
- 1085Immunophenotyping by Flow Cytometry IgG Heavy Chain Surface Test
- 1086Immunophenotyping by Flow Cytometry CD61 Test
- 1087Immunophenotyping by Flow Cytometry IgM Heavy Chain Surface Test
- 1088Immunophenotyping by Flow Cytometry Glycophorin Test
- 1089Immunophenotyping by Flow Cytometry: Leukemia Diagnostic Panel Acute Leukemia - T B or Myeloid Test
- 1090Immunophenotyping by Flow Cytometry: Double Negative T Cells (DNT) Test
- 1091Immunophenotyping by Flow Cytometry: Leukemia Diagnostic Panel- CLL/HCL/SLL Basic Test
- 1092Immunophenotyping by Flow Cytometry: Lymphoma Diagnostic Panel Test
- 1093Immunophenotyping by Flow Cytometry: Leukemia Diagnostic Panel-Plasma Cell Dyscrasias Test
- 1096Immunosuppressant Drug Profile 3 Test
- 1099Immunohistochemistry Microsatellite Instability Panel Test
- 1101Infertility Comprehensive Panel Females Test
- 1104Inhibin A Pregnancy Test
- 1106Inhibin B Test
- 1107Inhibin A Reproductive Marker Test
- 1110Insulin Post Prandial (PP) Test
- 1117Interleukin 28B rs12979860 & rs 8099917 Genotyping Qualitative PCR Test
- 1118Interferon - Beta IgG MAID Test
- 1121Interleukin-6 IL-6 Test
- 1126Iron Studies Monitoring Panel Test
- 1128JAK 2 Exon 12 Mutation Detection Test
- 1132JAK 2 V617F Reflex to JAK 2 Exon 12 Mutation Detection Test
- 1137Kappa / Lambda Light Chains Free Serum Test
- 1139Kappa / Lambda Light Chains Free Urine Test
- 1144Kidney Stone Formation Therapeutic Monitoring Panel Test
- 1145KRAS Codon 61 Mutation Detection Test
- 1150Lead Poisoning Panel Test
- 1151KRAS & NRAS Mutation Analysis Panel Test
- 1154Lactate Plasma Test
- 1155Lead Blood Test
- 1178Liver Fibrosis Panel Test
- 1179Listeria Antigen Stool Test
- 1182Liquid Biopsy cfDNA EGFR Test
- 1185Liver Panel 2 Test
- 1186Liver Panel 1 LFT Test
- 1188Expert Panel 2 Test
- 1189Expert Panel 3 Test
- 1190Expert Panel 1 Test
- 1191Expert Panel 4 Test
- 1196Lyme Disease (Borrelia Burgdorferi) IgG Immunoblot Test
- 1201Macrocytic Anemia Panel Test
- 1213Maternal Serum Screen 4 Quadruple Test Test
- 1226Metachromatic Leucodystrophy Quantitative Blood Test
- 1234Methylmalonic Acid Quantitative Serum Test
- 1236MI (Molecular Intelligence) Tumor Seek Test
- 1237Methylguanine Methyltransferase (MGMT) Test
- 1238MI (Molecular Intelligence) Profile Test
- 1245Minimal Residual Disease (MRD) Monitoring for B-CLL Test
- 1246Minimal Residual Disease (MRD) Analysis for B-ALL Test
- 1249Minimal Residual Disease (MRD) Monitoring for Multiple Myeloma Test
- 1253Mitotane Test
- 1256Microsatellite Instability (MSI) PCR Test
- 1258Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes (MELAS) Mutation Detection Test
- 1259Monoclonal Gammopathy of Undetermined Significance (MGUS) Panel Test
- 1262Multiple Sclerosis Panel 2 Test
- 1263Multiple Myeloma Screening Panel Test
- 1268Multiple Myeloma Monitoring Panel Test
- 1279Myeloproliferative Neoplasia (MPN) Extended Profile Test
- 1283Myositis Profile IgG: 11 Antigens Test
- 1284Myeloproliferative Neoplasia with Eosinophilia Test
- 1288NAFLD (Non-Alcoholic Fatty Liver Disease) Fibrosis Score Test
- 1289Neopterin Test
- 1290Neuron Specific Enolase (NSE) Serum Test
- 1296Newborn Screening Panel 4 Test
- 1297Neuronal (Paraneoplastic) Autoantibodies Profile Ultra Test
- 1298Neuroblastoma Profile 24 Hour Urine Test
- 1307Nicotine Screen Urine Test
- 1317NPM1 Gene Mutation Quantitative MRD Monitor Test
- 1318Nutritional Anemia Panel Test
- 1319Nx Gen Sequencing: Aicardi-Goutieres Syndrome Test
- 1321NRAS Mutation Codon 12 13 & 61 Test
- 1333Nx Gen Sequencing: Dementia Test
- 1342Nx Gen Sequencing: Maturity Onset Diabetes of Young (MODY) Test
- 1343Nx Gen Sequencing: Corneal Dystrophy Test
- 1346Nx Gen Sequencing: Megalencephalic Leukoencephalopathy with Subcortical Cysts Test
- 1347Nx Gen Sequencing: Ophthalmoplegia Test
- 1348Nx Gen Sequencing: Microphthalmia / Anophthalmia / Coloboma Spectrum Test
- 1349Nx Gen Sequencing: Optic Atrophy Test
- 1355Oncogenic E6/E7 mRNA Test
- 1356Oncomine Chronic Myeloid Leukaemia (CML) Panel Test
- 1362Oncopro BRAF Rapid Test
- 1363Oncomine Myeloproliferative Neoplasm (MPN) Panel Test
- 1364Oncopro Comprehensive Cancer Panel: 161 Genes Test
- 1365Oncopro EGFR Rapid Test
- 1366Oncopro 350 Gene TMB & MSI Profile Test
- 1367Oncopro Focus Fusion Panel for Solid Tumors Test
- 1368Oncomine Comprehensive Myeloid Panel Test
- 1369Oncopro EGFR ARMS PCR Test
- 1370Oncopro Tumor Mutation Burden (TMB) Test
- 1371Oncopro KRAS Rapid Test
- 1373Oncopro Lung Basic Panel Test
- 1374Opiates Screen Random Urine Test
- 1376Oncopro NCCN Lung Cancer Panel Test
- 1380Oncopro Liquid Biopsy Test
- 1385Prealbumin Test
- 1387Protein & Immunoglobulin Panel Test
- 1388Progesterone Serum Test
- 1394Pre-Operative Panel Test
- 1396Procainamide Test
- 1397Propoxyphene Screen Urine Test
- 1399Scrub Typhus (Tsutsugamushi) Antibody IgM Rapid Assay Test
- 1407Scrub Typhus (Tsutsugamushi) Antibody Test
- 1408SCA-3 (Spinocerebellar Ataxia): ATXN3 Gene Mutation Test
- 1410SCA-7 (Spinocerebellar Ataxia): ATXN7 Gene Mutation Test
- 1412Scleroderma Panel Test
- 1422Succinylacetone Urine Test
- 1423t(4;11) (q21;q23) (MLL-AF4) PCR Qualitative Test
- 1424Systemic Sclerosis Profile IgG Test
- 1426Syphilis Serology Test
- 1427T3 Reverse Test
- 1428t(11;19) (q23;p13.3) (MLL-ENL) PCR Qualitative Test
- 1429T Regulatory Cells (Tregs) Test
- 1430t(12;21) (p13;q22) ETV6-RUNX1 (TEL-AML1) PCR Qualitative Test
- 1437Tetanus Antitoxid Test
- 1438Thalassemia Alpha Trio Prenatal Mutation Detection Test
- 1446Transferrin Test
- 1453Transplant Infectious Screening Profile Test
- 1455Toxoplasma Avidity IgG Test
- 1463SLC24A5 Gene Albinism, Oculocutaneous Nonsyndromic NGS Genetic Test
- 1467Yeast (Candida Species) Identification Test
- 1477PXDN Gene Corneal Opacification and Other Ocular Anomalies NGS Genetic Test
- 1478VSX1 Gene Corneal Dystrophy, Posterior Polymorphous, Type 1 NGS Genetic Test
- 1483CHN1 Gene Duane Retraction Syndrome NGS Genetic Test
- 1484FZD4 Gene Exudative Vitreoretinopathy NGS Genetic Test
- 1496DHH Gene 46,XY Gonadal Dysgenesis, Partial, with Minifascicular Neuropathy NGS Genetic Test
- 1499ACOX1 Gene Acyl-CoA Peroxisomal Oxidase Deficiency NGS Genetic Test
- 1500RNASEH2C Gene Aicardi-Goutieres Syndrome Type 3 NGS Genetic Test
- 1501TREX1 Gene Aicardi-Goutieres Syndrome Type 1 NGS Genetic Test
- 1507DCPS Gene Al-Raqad Syndrome NGS Genetic Test
- 1509DNAJC3 Gene Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus NGS Genetic Test
- 1519PIK3R5 Gene Ataxia-Oculomotor Apraxia Type 3 NGS Genetic Test
- 1528EN2 Gene Autism Spectrum Disorder NGS Genetic Test
- 1530BIN1 Gene Centronuclear Myopathy Type 2 NGS Genetic Test
- 1533MYF6 Gene Centronuclear Myopathy Type 3 NGS Genetic Test
- 1548MFN2 Gene CMT2A2 NGS Genetic Test
- 1550RAB7A Gene CMT2B NGS Genetic Test
- 1556KIF1B Gene CMT2A1 NGS Genetic Test
- 1564TMEM67 Gene COACH syndrome NGS Genetic Test
- 1571B3GALNT2 Gene Congenital muscular dystrophy and hypoglycosylation of α-dystroglycan NGS Genetic Test
- 1574PRRT2 Gene Convulsions, familial infantile, with paroxysmal choreoathetosis NGS Genetic Test
- 1576SLC2A1 Gene DYT18 NGS Genetic Test
- 1578TIMM8A Gene Dystonia-deafness syndrome NGS Genetic Test
- 1585ATP1A3 Gene DYT12 NGS Genetic Test
- 1587COL6A3 Gene DYT27 NGS Genetic Test
- 1588GNAL Gene DYT25 NGS Genetic Test
- 1590GABRA1 Gene Early infantile epileptic encephalopathy type 19 NGS Genetic Test
- 1602DOCK7 Gene Early infantile epileptic encephalopathy type 23 NGS Genetic Test
- 1607MED12 Gene FG syndrome type 1 NGS Genetic Test
- 1610ETHE1 Gene Ethylmalonic encephalopathy NGS Genetic Test
- 1614FLNC Gene Filaminopathy NGS Genetic Test
- 1623FMR1 Gene Fragile X syndrome NGS Genetic Test
- 1624FLNA Gene Frontometaphyseal dysplasia NGS Genetic Test
- 1626FUCA1 Gene Fucosidosis NGS Genetic Test
- 1627FKTN Gene Fukuyama congenital muscular dystrophy NGS Genetic Test
- 1632TMEM138 Gene Joubert syndrome type 16 NGS Genetic Test
- 1634TBR1 Gene Intellectual disability, TBR1 related NGS Genetic Test
- 1638CPLANE1 Gene Joubert syndrome type 17 NGS Genetic Test
- 1649KIAA0586 Gene Joubert syndrome type 23 NGS Genetic Test
- 1658GBA Gene Lewy body dementia, susceptibility to NGS Genetic Test
- 1670POMK Gene Limb-girdle muscular dystrophy, autosomal recessive type 12C NGS Genetic Test
- 1676KLF8 Gene Mental retardation non-syndromic NGS Genetic Test
- 1681ZCCHC12 Gene Mental retardation non-syndromic NGS Genetic Test
- 1690MID2 Gene Mental retardation, X-linked type 101 NGS Genetic Test
- 1692HUWE1 Gene Mental retardation, X-linked syndromic, Turner type NGS Genetic Test
- 1712SMS Gene Mental retardation, X-linked, Snyder-Robinson type NGS Genetic Test
- 1718UQCRB Gene Mitochondrial complex III deficiency NGS Genetic Test
- 1735TK2 Gene Mitochondrial DNA depletion syndrome NGS Genetic Test
- 1740EPM2A Gene Myoclonic epilepsy of Lafora NGS Genetic Test
- 1741DRD2 Gene Myoclonic dystonia, DRD2 related NGS Genetic Test
- 1747AMPD1 Gene Myopathy due to myoadenylate deaminase deficiency NGS Genetic Test
- 1762WDR45 Gene Neurodegeneration with brain iron accululation type 5 NGS Genetic Test
- 1763CFL2 Gene Nemaline myopathy type 7 NGS Genetic Test
- 1767CNTNAP4 Gene Neurodevelopmental disorder, CNTNAP4 related NGS Genetic Test
- 1768ACTA1 Gene Nemaline myopathy type 3 NGS Genetic Test
- 1772MACF1 Gene Neurodevelopmental disorder, MACF1 related NGS Genetic Test
- 1774NGEF Gene Neurodevelopmental disorder, NGEF related NGS Genetic Test
- 1789ATP13A2 Gene PARK9 Parkinson NGS Genetic Test
- 1791ZFHX4 Gene Ptosis, congenital NGS Genetic Test
- 1800CERS1 Gene Progressive myoclonus epilepsy type 8 NGS Genetic Test
- 1802CAV3 Gene Rippling muscle disease NGS Genetic Test
- 1807NOTCH4 Gene Schizophrenia, NOTCH4 related NGS Genetic Test
- 1810C12ORF65 Gene SPG55 NGS Genetic Test
- 1813AP4S1 Gene SPG52 NGS Genetic Test
- 1818TFG Gene SPG57 NGS Genetic Test
- 1822ARSI Gene SPG66, ARSI related NGS Genetic Test
- 1825SPG7 Gene SPG7 NGS Genetic Test
- 1828WASHC5 Gene SPG8 NGS Genetic Test
- 1831ITPR1 Gene Spinocerebellar ataxia type 15 NGS Genetic Test
- 1833KCND3 Gene Spinocerebellar ataxia type 22, autosomal dominant NGS Genetic Test
- 1838EEF2 Gene Spinocerebellar ataxia type 26, autosomal dominant NGS Genetic Test
- 1839AFG3L2 Gene Spinocerebellar ataxia type 28, autosomal dominant NGS Genetic Test
- 1841BEAN1 Gene Spinocerebellar ataxia type 31, autosomal dominant NGS Genetic Test
- 1847PEX13 Gene Zellweger syndrome NGS Genetic Test
- 1848Lysosomal Storage Disorders Enzyme Panel NGS Genetic Test
- 1849Newborns Genetic Test Panel NGS Genetic Test
- 1852PEX2 Gene Zellweger syndrome NGS Genetic Test
- 1862Sphingo Enzyme Panel NGS Genetic Test
- 1871ETFA Gene Acyl-CoA multiple dehydrogenase deficiency NGS Genetic Test
- 1875ACADM Gene Acyl-CoA medium-chain dehydrogenase deficiency NGS Genetic Test
- 1878CYP11B1 Gene Adrenal hyperplasia due to steroid 11-beta-hydroxylase deficiency NGS Genetic Test
- 1888GBE1 Gene Andersen disease NGS Genetic Test
- 1893ABCD3 Gene Bile acid synthesis defect type 5, congenital NGS Genetic Test
- 1919ABCB11 Gene Cholestasis progressive intrahepatic type 2 NGS Genetic Test
- 1927SLC25A13 Gene Citrin deficiency NGS Genetic Test
- 1939GTPBP3 Gene Combined oxidative phosphorylation deficiency type 23 NGS Genetic Test
- 1944C12ORF65 Gene Combined oxidative phosphorylation deficiency type 7 NGS Genetic Test
- 1947AIFM1 Gene Combined oxidative phosphorylation deficiency type 6 NGS Genetic Test
- 1948AARS2 Gene Combined oxidative phosphorylation deficiency type 8 NGS Genetic Test
- 1953CPOX Gene Coproporphyria NGS Genetic Test
- 1963MRPS22 Gene Combined oxidative phosphorylation deficiency type 5 NGS Genetic Test
- 1967SLC26A3 Gene Diarrhea type 1, secretory chloride, congenital NGS Genetic Test
- 1975F13B Gene Factor XIIIB deficiency NGS Genetic Test
- 1980FANCD2 Gene Fanconi anemia type D2 NGS Genetic Test
- 1992SLC2A2 Gene Fanconi-Bickel syndrome NGS Genetic Test
- 2001GBA Gene Gaucher disease type 1 NGS Genetic Test
- 2004ABCB4 Gene Gallbladder disease type 1 NGS Genetic Test
- 2011GCDH Gene Glutaric acidemia type 1 NGS Genetic Test
- 2015GSS Gene Glutathione synthetase deficiency NGS Genetic Test
- 2022GYG1 Gene Glycogen storage disease type 15 NGS Genetic Test
- 2026G6PC Gene Glycogen storage disease type 1A NGS Genetic Test
- 2040MPDU1 Gene Glycosylation disorder type 1F NGS Genetic Test
- 2043DOLK Gene Glycosylation disorder type 1M NGS Genetic Test
- 2057TMEM165 Gene Glycosylation disorder type 2K NGS Genetic Test
- 2073LARS2 Gene Hydrops, lactic acidosis, and sideroblastic anemia NGS Genetic Test
- 2082EPHX2 Gene Hypercholesterolemia, familial, due to LDLR defect, modifier of NGS Genetic Test
- 2088KCNJ11 Gene Hyperinsulinemic hypoglycemia type 2 NGS Genetic Test
- 2091LPL Gene Hyperlipoproteinemia type 1 NGS Genetic Test
- 2106PTS Gene Hyperphenylalaninemia, BH4-deficient, type A NGS Genetic Test
- 2119SLC2A9 Gene Hypouricemia, renal type 2 NGS Genetic Test
- 2122ACADL Gene LCAD deficiency NGS Genetic Test
- 2126FGF23 Gene Hypophosphatemic rickets, autosomal dominant NGS Genetic Test
- 2127HADHA Gene Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency NGS Genetic Test
- 2133MBL2 Gene Mannose-binding protein deficiency NGS Genetic Test
- 2141DLD Gene Maple syrup urine disease type 3 NGS Genetic Test
- 2165MMAA Gene Methylmalonic aciduria CblA type NGS Genetic Test
- 2167MVK Gene Mevalonic aciduria NGS Genetic Test
- 2169MCEE Gene Methylmalonyl-CoA epimerase deficiency NGS Genetic Test
- 2177IDS Gene Mucopolysaccharidosis type 2 NGS Genetic Test
- 2179HGSNAT Gene Mucopolysaccharidosis type 3C NGS Genetic Test
- 2197UMPS Gene Orotic aciduria NGS Genetic Test
- 2202AMPD1 Gene Myopathy due to myoadenylate deaminase deficiency NGS Genetic Test
- 2206PHGDH Gene Phosphoglycerate dehydrogenase deficiency NGS Genetic Test
- 2208PCK2 Gene Phosphoenolpyruvate carboxykinase deficiency, mitochondrial NGS Genetic Test
- 2209SLC7A5 Gene Phenylketonuria modifier, SLC7A5 related NGS Genetic Test
- 2235SLC52A1 Gene Riboflavin deficiency NGS Genetic Test
- 2237CYP2R1 Gene Rickets, vitamin D 25-hydroxylation-deficient, type 1B NGS Genetic Test
- 2239HEXB Gene Sandhoff disease NGS Genetic Test
- 2241NAGA Gene Schindler disease NGS Genetic Test
- 2243SERHL2 Gene Serine hydrolase deficiency, SERHL2 related NGS Genetic Test
- 2246SUMF1 Gene Sulfatase deficiency NGS Genetic Test
- 2249SFTPB Gene Surfactant metabolism dysfunction type 1 NGS Genetic Test
- 2252ABCA3 Gene Surfactant metabolism dysfunction type 3 NGS Genetic Test
- 2254HEXA Gene Tay-Sachs disease NGS Genetic Test
- 2259GM2A Gene Tay-Sachs disease AB variant NGS Genetic Test
- 2261TCN2 Gene Transcobalamin II deficiency NGS Genetic Test
- 2264HADHA Gene Trifunctional protein deficiency NGS Genetic Test
- 2266FAH Gene Tyrosinemia type 1 NGS Genetic Test
- 2269TAT Gene Tyrosinemia type 2 NGS Genetic Test
- 2276COL4A5 Gene Alport syndrome, X-Linked NGS Genetic Test
- 2285SLC52A2 Gene Brown-Vialetto-Van Laere syndrome type 2 NGS Genetic Test
- 2291CATSPER2 Gene Deafness and male infertility, CATSPER2 related NGS Genetic Test
- 2292MYO7A Gene Deafness, autosomal dominant type 11 NGS Genetic Test
- 2297EYA4 Gene Deafness, autosomal dominant type 10 NGS Genetic Test
- 2312CEACAM16 Gene Deafness, autosomal dominant type 4B NGS Genetic Test
- 2316DIABLO Gene Deafness, autosomal dominant type 64 NGS Genetic Test
- 2330TRIOBP Gene Deafness, autosomal recessive type 28 NGS Genetic Test
- 2331GRXCR1 Gene Deafness, autosomal recessive type 25 NGS Genetic Test
- 2337MYO3A Gene Deafness, autosomal recessive type 30 NGS Genetic Test
- 2347COL11A1 Gene Marshall syndrome NGS Genetic Test
- 2358IKBKG Gene Atypical Mycobacterial infection NGS Genetic Test
- 2370FASLG Gene Autoimmune lymphoproliferative syndrome type 1B NGS Genetic Test
- 2371FAS Gene Autoimmune lymphoproliferative syndrome type 1A NGS Genetic Test
- 2372CASP10 Gene Autoimmune lymphoproliferative syndrome type 2A NGS Genetic Test
- 2375NLRC4 Gene Cold autoinflammatory syndrome type 4, familial NGS Genetic Test
- 2379LYST Gene Chediak-Higashi syndrome NGS Genetic Test
- 2385P4HB Gene Cole-Carpenter syndrome type 1 NGS Genetic Test
- 2387PLEC Gene Epidermolysis bullosa simplex with pyloric atresia NGS Genetic Test
- 2404COMP Gene Epiphyseal dysplasia, multiple, type 1 NGS Genetic Test
- 2405LAMB3 Gene Epidermolysis bullosa, junctional, non-Herlitz type NGS Genetic Test
- 2406KRT10 Gene Epidermolytic hyperkeratosis NGS Genetic Test
- 2409EXPH5 Gene Epidermolysis bullosa, nonspecific, autosomal recessive NGS Genetic Test
- 2410KRT9 Gene Epidermolytic palmoplantar keratoderma NGS Genetic Test
- 2413CERS3 Gene Ichthyosis, congenital, autosomal recessive, type 9 NGS Genetic Test
- 2417ABCA12 Gene Ichthyosis, lamellar type 2 NGS Genetic Test
- 2429TGFBR2 Gene Marfan syndrome, TGFBR2 related NGS Genetic Test
- 2433TGFBR2 Gene Loeys-Dietz syndrome type 2B NGS Genetic Test
- 2439MKKS Gene McKusick-Kaufman syndrome NGS Genetic Test
- 2440TGFBR1 Gene Loeys-Dietz syndrome type 2A NGS Genetic Test
- 2443AP1S1 Gene MEDNIK syndrome NGS Genetic Test
- 2445MT-TP Gene MERRF syndrome, MT-TP related NGS Genetic Test
- 2447COL10A1 Gene Metaphyseal chondrodysplasia, Schmid type NGS Genetic Test
- 2448CLCN7 Gene Osteopetrosis, autosomal recessive type 4 NGS Genetic Test
- 2449P3H1 Gene Osteogenesis imperfecta type 8 NGS Genetic Test
- 2453IL1RN Gene Osteomyelitis, sterile multifocal, with periostitis and pustulosis NGS Genetic Test
- 2455SNX10 Gene Osteopetrosis of infancy, malignant NGS Genetic Test
- 2456TNFSF11 Gene Osteopetrosis, autosomal recessive type 2 NGS Genetic Test
- 2458PPIB Gene Osteogenesis imperfecta type 9 NGS Genetic Test
- 2461CLCN7 Gene Osteopetrosis, autosomal dominant type 1 NGS Genetic Test
- 2463AFF3 Gene Rheumatoid arthritis, susceptibility to NGS Genetic Test
- 2464VDR Gene Rickets, vitamin D-resistant, type 2A NGS Genetic Test
- 2466PTPRC Gene Severe combined immunodeficiency, T cell-negative, B-cell/natural killer-cell positive NGS Genetic Test
- 2467TNFAIP3 Gene Rheumatoid arthritis, TNFAIP3 related NGS Genetic Test
- 2478DSP Gene Skin fragility-woolly hair syndrome NGS Genetic Test
- 2480IL7R Gene Severe combined immunodeficiency, T-cell negative, B-cell/natural killer cell-positive type NGS Genetic Test
- 2481FLNB Gene Spondylocarpotarsal synostosis syndrome NGS Genetic Test
- 2483DLL3 Gene Spondylocostal dysostosis, autosomal recessive type 1 NGS Genetic Test
- 2484SLC39A13 Gene Spondylocheirodysplasia, Ehlers-Danlos syndrome-like NGS Genetic Test
- 2488ERCC4 Gene XFE progeroid syndrome NGS Genetic Test
- 2489GJA5 Gene Atrial fibrillation type 11 NGS Genetic Test
- 2491DSP Gene Arrhythmogenic right ventricular cardiomyopathy type 8 NGS Genetic Test
- 2492SCN5A Gene Atrial fibrillation type 10 NGS Genetic Test
- 2493Pulmonary panel NGS Genetic Test
- 2495TMEM43 Gene Arrhythmogenic right ventricular cardiomyopathy type 5 NGS Genetic Test
- 2497FOXF1 Gene Alveolar capillary dysplasia with misalignment of pulmonary veins NGS Genetic Test
- 2504COA5 Gene Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency type 3 NGS Genetic Test
- 2508PPP1R8 Gene Cardiac defects, PPP1R8 related NGS Genetic Test
- 2510FLNA Gene Cardiac valvular dysplesia, X-linked NGS Genetic Test
- 2515MAP2K2 Gene Cardiofaciocutaneous syndrome type 4 NGS Genetic Test
- 2520MYOZ2 Gene Cardiomyopathy, familial hypertrophic type 16 NGS Genetic Test
- 2521DSP Gene Cardiomyopathy, dilated with woolly hair and keratoderma NGS Genetic Test
- 2536SCN5A Gene Long QT syndrome type 3 NGS Genetic Test
- 2538MT-TC Gene MELAS syndrome NGS Genetic Test
- 2539MT-TS1 Gene MERRF/MELAS overlap syndrome, MT-TS1 related NGS Genetic Test
- 2540FBN1 Gene MASS syndrome NGS Genetic Test
- 2544CALM2 Gene Long QT syndrome type 15 NGS Genetic Test
- 2546SERPING1 Gene Angioedema, hereditary NGS Genetic Test
- 2547TGFBR1 Gene Aortic aneurysm, familial thoracic type 5 NGS Genetic Test
- 2549PRKG1 Gene Aortic aneurysm, familial thoracic type 8 NGS Genetic Test
- 2550SLC2A10 Gene Arterial Tortuosity Syndrome NGS Genetic Test
- 2551MYH11 Gene Aortic aneurysm, familial thoracic type 4 NGS Genetic Test
- 2555SOAT1 Gene Atherosclerosis, SOAT1 related NGS Genetic Test
- 2556NOTCH1 Gene Aortic valve disease type 1 NGS Genetic Test
- 2557TGFBR2 Gene Aortic aneurysm, familial thoracic type 3 NGS Genetic Test
- 2561BSND Gene Bartter syndrome type 4a NGS Genetic Test
- 2562CLCNKB Gene Bartter syndrome type 3 NGS Genetic Test
- 2563SLC12A7 Gene Bartter syndrome NGS Genetic Test
- 2564SLC12A5 Gene Bartter syndrome NGS Genetic Test
- 2565LZTFL1 Gene Bardet-Biedl syndrome, LZTFL1 related NGS Genetic Test
- 2578PREPL Gene Cystinuria NGS Genetic Test
- 2580ABCC2 Gene Dubin-Johnson syndrome NGS Genetic Test
- 2581CTNS Gene Cystinosis, nephropathic NGS Genetic Test
- 2584MYH9 Gene Epstein syndrome NGS Genetic Test
- 2587ICK Gene Endocrine-cerebroosteodysplasia NGS Genetic Test
- 2591TBCE Gene Hypoparathyroidism-retardation-dysmorphism syndrome NGS Genetic Test
- 2592CLCN5 Gene Hypophosphatemic rickets NGS Genetic Test
- 2598MCM4 Gene Immunodeficiency with natural killer cell deficiency NGS Genetic Test
- 2599PAX8 Gene Hypothyroidism congenital nongoitrous type 2, familial NGS Genetic Test
- 2600NBAS Gene Infantile liver failure syndrome type 2 NGS Genetic Test
- 2602MAGT1 Gene Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia NGS Genetic Test
- 2609GHR Gene Laron syndrome NGS Genetic Test
- 2610SEMA3A Gene Kallmann syndrome, SEMA3A related NGS Genetic Test
- 2617OCRL Gene Lowe oculocerebrorenal syndrome NGS Genetic Test
- 2618PCSK1 Gene Obesity with impaired prohormone processing NGS Genetic Test
- 2621NEK8 Gene Nephronophthisis type 9 NGS Genetic Test
- 2628LAMB2 Gene Nephrotic syndrome type 5 NGS Genetic Test
- 2633POMC Gene Obesity, early-onset, susceptibility to NGS Genetic Test
- 2635PPARG Gene Obesity, severe NGS Genetic Test
- 2636SLC4A1 Gene Ovalocytosis NGS Genetic Test
- 2637AGTR1 Gene Renal tubular dysgenesis NGS Genetic Test
- 2641SDCCAG8 Gene Senior-Loken syndrome type 7 NGS Genetic Test
- 2643DUOX2 Gene Thyroid dyshormonogenesis type 6 NGS Genetic Test
- 2644IYD Gene Thyroid dyshormonogenesis type 4 NGS Genetic Test
- 2648RBM8A Gene Thromocytopenia-Absent-Radius-Syndrome NGS Genetic Test
- 2653THRB Gene Thyroid hormone resistance NGS Genetic Test
- 2662RPL26 Gene Diamond-Blackfan anemia type 11 NGS Genetic Test
- 2666RPS19 Gene Diamond-Blackfan anemia type 1 NGS Genetic Test
- 2669SRP72 Gene Bone marrow failure syndrome type 1 NGS Genetic Test
- 2672EPAS1 Gene Erythrocytosis, familial type 4 NGS Genetic Test
- 2675F2 Gene Dysprothrombinemia NGS Genetic Test
- 2676C15orf41 Gene Dyserythropoietic anemia, congenital, type 1B NGS Genetic Test
- 2677F10 Gene Factor X deficiency NGS Genetic Test
- 2684KLF1 Gene Dyserythropoietic anemia, congenital, type 4 NGS Genetic Test
- 2686NCF2 Gene Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2 NGS Genetic Test
- 2687CYCS Gene Thrombocytopenia type 4 NGS Genetic Test
- 2691MASTL Gene Thrombocytopenia type 2 NGS Genetic Test
- 2696ITGA2B Gene Thrombocytopenia, neonatal alloimmune NGS Genetic Test
- 2703MNX1 Gene Currarino syndrome NGS Genetic Test
- 2705COL2A1 Gene Czech dysplasia NGS Genetic Test
- 2710ANKH Gene Craniometaphyseal dysplasia NGS Genetic Test
- 2713VSX1 Gene Craniofacial anomalies and anterior segment dysgenesis syndrome NGS Genetic Test
- 2714FGFR2 Gene Crouzon syndrome NGS Genetic Test
- 2715LAMC1 Gene Dandy-Walker malformation and occipital cephaloceles, LAMC1 related NGS Genetic Test
- 2725TSR2 Gene Diamond-Blackfan anemia type 14 with mandibulofacial dysostosis NGS Genetic Test
- 2728SALL4 Gene Duane Retraction syndrome NGS Genetic Test
- 2732DOK7 Gene Fetal akinesia deformation sequence NGS Genetic Test
- 2735RAPSN Gene Fetal akinesia deformation sequence NGS Genetic Test
- 2736BCS1L Gene GRACILE syndrome NGS Genetic Test
- 2737FGD1 Gene Faciogenital dysplasia NGS Genetic Test
- 2738MYCN Gene Feingold syndrome NGS Genetic Test
- 2740WDR73 Gene Galloway-Mowat syndrome NGS Genetic Test
- 2741LBR Gene Greenberg skeletal dysplasia NGS Genetic Test
- 2743FH Gene Fumarase deficiency NGS Genetic Test
- 2744ERCC4 Gene Fanconi anemia, complementation group Q NGS Genetic Test
- 2745SATB2 Gene Glass syndrome NGS Genetic Test
- 2748LAMB1 Gene Lissencephaly type 5 NGS Genetic Test
- 2750FLNB Gene Larsen syndrome NGS Genetic Test
- 2753TUBA1A Gene Lissencephaly type 3 NGS Genetic Test
- 2754MYBPC1 Gene Lethal congenital contracture syndrome type 4 NGS Genetic Test
- 2757RELN Gene Lissencephaly type 2 (Norman-Roberts type) NGS Genetic Test
- 2759FGFR2 Gene LADD syndrome NGS Genetic Test
- 2764PHC1 Gene Microcephaly, autosomal recessive type 11 NGS Genetic Test
- 2765CENPJ Gene Microcephaly, autosomal recessive type 6 NGS Genetic Test
- 2770CDK5RAP2 Gene Microcephaly, autosomal recessive type 3 NGS Genetic Test
- 2774RTTN Gene Microcephaly, short stature, and polymicrogyria with seizures NGS Genetic Test
- 2777TUBB2B Gene Microcephaly, TUBB2B related NGS Genetic Test
- 2779UQCC2 Gene Mitochondrial complex III deficiency, nuclear type 7 NGS Genetic Test
- 2780HNRNPU Gene RNA processing related disorders NGS Genetic Test
- 2781AGPS Gene Rhizomelic chondrodysplasia punctata type 3 NGS Genetic Test
- 2782FOXG1 Gene Rett syndrome, congenital variant NGS Genetic Test
- 2783RDH11 Gene Retinal dystrophy, juvenile cataracts, and short stature syndrome NGS Genetic Test
- 2787PEX5 Gene Rhizomelic chondrodysplasia punctata type 5 NGS Genetic Test
- 2788ESCO2 Gene Roberts syndrome NGS Genetic Test
- 2792WASHC5 Gene Ritscher-Schinzel syndrome type 1 NGS Genetic Test
- 2796CREBBP Gene Rubinstein-Taybi syndrome NGS Genetic Test
- 2798TWIST1 Gene Saethre-Chotzen syndrome NGS Genetic Test
- 2807NIN Gene Seckel syndrome type 7 NGS Genetic Test
- 2808NHEJ1 Gene Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation NGS Genetic Test
- 2812NEK1 Gene Short-rib thoracic dysplasia type 6 with or without polydactyly NGS Genetic Test
- 2816WDR60 Gene Short-rib thoracic dysplasia type 8 with or without polydactyly NGS Genetic Test
- 2817DYNC2H1 Gene Short-rib thoracic dysplasia type 3 with or without polydactyly NGS Genetic Test
- 2822chr. 11p15 Gene Silver-Russell syndrome NGS Genetic Test
- 2823ERCC4 Gene XFE progeroid syndrome NGS Genetic Test
- 2829Cancer comprehensive panel NGS Genetic Test
- 2832Colon Cancer comprehensive panel NGS Genetic Test
- 2833OncoDx panel NGS Genetic Test
- 2837H19 Gene Beckwith-Wiedemann syndrome NGS Genetic Test
- 2839BRAF Gene BRAF, selective sequencing of exon 15 NGS Genetic Test
- 2840PALB2 Gene Breast cancer, susceptibility to NGS Genetic Test
- 2851MSH6 Gene Colorectal cancer, hereditary nonpolyposis type 5 NGS Genetic Test
- 2855PMS2 Gene Colorectal cancer, hereditary nonpolyposis type 4 NGS Genetic Test
- 2857AKT1 Gene Cowden syndrome type 6 NGS Genetic Test
- 2860PIK3CA Gene Cowden syndrome type 5 NGS Genetic Test
- 2864APC Gene Desmoid disease, hereditary NGS Genetic Test
- 2869RB1 Gene Hereditary Retinoblastoma NGS Genetic Test
- 2870NTHL1 Gene Familial adenomatous polyposis type 3 NGS Genetic Test
- 2872MUTYH Gene Familial adenomatous polyposis type 2 NGS Genetic Test
- 2874IDH1 Gene IDH1, selective sequencing of exon 4 NGS Genetic Test
- 2880IDH2 Gene IDH2, selective sequencing of exon 4 NGS Genetic Test
- 2882BMPR1A Gene Juvenile polyposis syndrome NGS Genetic Test
- 2888CEBPA Gene Leukemia, acute myeloid, somatic NGS Genetic Test
- 2892XRCC3 Gene Melanoma, cutaneous malignant, familial type 6, susceptibility to NGS Genetic Test
- 2896PDGFB Gene Meningioma, familial, PDGFB related NGS Genetic Test
- 2899SUFU Gene Meningioma, familial, susceptibility to NGS Genetic Test
- 2907CDKN1B Gene Multiple endocrine neoplasia type 4 NGS Genetic Test
- 2913SPRED1 Gene Neurofibromatosis type 1 -like syndrome NGS Genetic Test
- 2916NF1 Gene Neurofibromatosis type 1 NGS Genetic Test
- 2917NRAS Gene NRAS, selective sequencing of exons 2 and 3 NGS Genetic Test
- 2920SDHD Gene Paragangliomas type 1, with or without deafness NGS Genetic Test
- 2922CDKN2A Gene Pancreatic cancer/melanoma syndrome, familial NGS Genetic Test
- 2923SDHA Gene Paragangliomas type 5 NGS Genetic Test
- 2927TMEM127 Gene Pheochromocytoma type 8 NGS Genetic Test
- 2930MAX Gene Pheochromocytoma type 9 NGS Genetic Test
- 2931Acute Leukemia Panel
- 29321p & 19q Test
- 2934ALK/EML4 (NSCLC)
- 2935ALL FISH PANEL [FISH [BCR/ABL, TEL/AML1, MLL, E2A])
- 2936ALL PANEL (Cytogenetics + FISH [BCR/ABL, TEL/AML1, MLL, E2A])
- 2939ALL Panel Deletion/Duplication Detection
- 2941RNASEL Gene Prostate cancer, hereditary type 1 NGS Genetic Test
- 2942Achondroplasia (FGFR3 Full Gene Sequence Analysis)
- 2946Bone Marrow Biopsy
- 2947Cardiomyopathy Gene Panel
- 2948Biopsy Uterus with Adnexa and Fibroid
- 2949Biopsy Uterus with Cervix
- 2954Acute Leukemia Mini Panel (AML/ETO, INV[16], PML/RARA, BCR/ABL, TEL/AML1, MLL, E2A)
- 2957CALR Mutation Analysis (Deletion or Insertion in Exon 9)
- 2960CCND1
- 2961Chromosome Breakage Syndrome
- 2962cKIT Mutation Screening (Exons 9, 11, 13, 17) Gastrointestinal Stromal Tumors
- 2963CLL FISH Panel (FISH [del(11q), trisomy 12, del(13q), del(17p)])
- 2964CCDN1
- 2965Chromosomes 13 & 21
- 2966Chromosome 21
- 2969Chronic Leukemia Panel
- 2973CLL Panel (Cytogenetics + FISH [del(11q), trisomy 12, del(13q), del(17p)])
- 2975CLL Panel Deletion/Duplication Detection
- 2976Common Neurological/Neuromuscular Diseases Gene Panel
- 2978Comprehensive Hereditary Cancer Panel (154 Genes)
- 2980CYTOLOGY- LBC PAP SMEAR
- 2982Cystic Fibrosis Mutation Screening (CFTR - Del 508)
- 2984CRLF2 (CML, AML, ALL)
- 2985Complete Inherited Disease Panel
- 2987Congenital Myopathy Gene Panel
- 2989Deafness Gene Panel
- 2990Del(20q) (MDS)
- 2993EWSR1 Gene (Ewing's Sarcoma)
- 2995FGFR1(Solid Tumor)
- 3002FGFR3/IgH (MM)
- 3003Epstein Barr Virus Quantitative PCR
- 3004Fine Needle Aspiration Cytology- Effusion Cytology+Cell Block
- 3005Fine Needle Aspiration Cytology- Prepared 6 Slides
- 3006Fine Needle Aspiration Cytology- Slide For Review 18-24 Slides
- 3007Fine Needle Aspiration Cytology- Slide For Review 12-18 Slides
- 3008Fine Needle Aspiration Cytology- Procedure With Reporting
- 3009Fine Needle Aspiration Cytology- Slide For Review 30-35 Slides
- 3010Fine Needle Aspiration Cytology- Slide For Review 24-30 Slides
- 3011Fluid Cytology (Urine/CSF/Cytology)
- 3013Fine Needle Aspiration Cytology- Slide For Review 6-12 Slides
- 3014Frozen-1
- 3015FOXO1 Break Apart FISH Alveolar Rhabdomyosarcoma Diagnostic
- 3020Haemophilia A & B Gene Panel
- 3021HbE (Hemoglobin E) Mutation Screening
- 3032Her-2 Neu (Ca Breast)
- 3034Hepatitis-C Virus (HCV) Quantitative PCR
- 3037HLA A, B, C, DRB1, DQB1 (Any One) [Low Resolution]
- 3039HLA A, B, C, DRB1, DQB1 [Low Resolution]
- 3041HLA A, B, DRB1 [Low Resolution]
- 3048IHC Any Single Marker (HER2NEU/C4D/EBER/Ki67)
- 3049Iamp (21)
- 3051IgH (MM)
- 3053IHC ER-PR
- 3054IGVH Mutation Load
- 3055IHC ER+PR+HER2NEU+KI67
- 3056Irnotecan Toxicity Assessment (UGT1A1 Genotyping)/ Gilbert Syndrome
- 3057JAK2 Gene (V617F) Quantitative
- 3058IHC ER-PR,HER2NEU
- 3059IHC Up to 5 Markers
- 3060IRFA-MUM1
- 3062IHC Extended Panel (>10Markers)-
- 3063Large Biopsy (4) Radical Prostatectomy, Whipple's
- 3064Jak 2 Mutation Detection Panel (Exons 12)
- 3065Large Biopsy (3)
- 3066Karyotyping for Detection of Fragile X Syndrome
- 3067KRAS,NRAS
- 3068Large Biopsy (1)
- 3069Large Biopsy (2)-All Cancer Resection
- 3071Large Biopsy (5) Post Chemotherapy Bone
- 3072Large Biopsy (6)- Amputation
- 3073Large Biopsy (7)
- 3074Large Biopsy (8)
- 3076Metabolic Disorder Gene Panel
- 3077Microarray 60K (AF/CVS/CB) + Karyotyping + FISH chromosome 13,18,21, X and Y
- 3078Medium Biopsy(4)
- 3082Microarray 60K (AF/CVS) + Karyotyping
- 3086MET Amplification (NSCLC)
- 3088DNA Genetic Methylation Test
- 3091MLC1 Gene Mutation Analysis (Agrawal Mutation)
- 3097Microarray 60K (POC)+ Single Karyotying
- 3098MLL (AML, ALL)
- 3099Mycobacterium Tuberculosis Qualitative PCR
- 3100Multiplex Panel (Cytogenetics & PCR for 28 translocations & 80 breakpoints) (CML, AML, ALL)
- 3104MM FISH Panel (FISH[del(11q), del(13q), IgH, del(17p)]
- 3106NGS Homologous Recombinant Deficiency [HRR] Panel
- 3109NGS TP53 Mutation Analysis
- 3110N-Myc Oncogene
- 3115NRAS Mutation Analysis (Codons 12 & 13)
- 3117MLL t(4;11)(q21;q23) Qualitative
- 3118NPM1+FLT3
- 3119NTRK1
- 3121NTRK1+NTRK2+NTRK3
- 3123NTRK2
- 3124Oncomine Breast cfTNA Assay
- 3126Oncomine Comprehensive Panel + Oncomine Tumor Mutation Burden (TMB)+ MSI + PDL1
- 3127Oncomine Comprehensive Panel + Oncomine Tumor Mutation Burden + MSI
- 3131Oncomine Lung cfTNA Cancer Panel
- 3136Oncomine Tumor Mutation Burden [TMB] + Microsatellite Instability (MSI)
- 3139PDGFR Mutation Screening (Exons 12, 14, 18)
- 3140Oncomine Focus Panel + PDL1
- 3141PDGFR? (HES)
- 3142PDL1 Dako
- 3143Peripheral Blood for High Resolution Single Karyotyping
- 3144PDGFR
- 3146PDL-1 [SP263 Clone]
- 3154PML/RARA Quantitative [Single Form]
- 3156Prader-Willi Syndrome (FISH)
- 3157PNH Comprehensive Work Up (Flow Cytometry)-Flaer, CD14, CD15, CD24, CD45,CD59, CD64, GlY-A
- 3158Pre-Implantation Genetic Disorder/PGD (Single Embryo)
- 3161Pre-Implantation Genetic Disorder/PGD (Single Embryo) with Maternal DNA Contamination Check
- 3162Pre-Implantation Genetic Screening /PGS (per Embryo)
- 3163Pre-Implantation Genetic Disorder/PGD (Single Gene Disorder- Known Mutation)- Baseline
- 3172RB1 Gene Deletion & Duplication Detection (Retinoblastoma)
- 3178Replication Factor C1 Mutation Screening (RFC1 - 80G>A)
- 3181RETT Syndrome Deletion & Duplication Detection
- 3182Review of 1 Slide and Block
- 3183Review of >20 Slide and Block
- 3184Review of 15-20 Slide and Block
- 3186Review of 4-6 Slide and Block
- 3187Review of 2 Slide and Block
- 3188Review of 3 Slide and Block
- 3189ROS 1 (NSCLC)
- 3190Sarcoma Gene Panel
- 3193Small Biopsy (1) Punch Biopsy, GI Biopsy, Gall Bladder, Appendix, D&C, Bone Marrow.
- 3196Small Biopsy Bottle No 10
- 3197Small Biopsy Bottle No 1
- 3198Small Biopsy Bottle No 11
- 3199Small Biopsy Bottle No 12
- 3200Review of 7-9 Slide and Block
- 3202Small Biopsy Bottle No 3
- 3204Small Biopsy Bottle No 2
- 3205Small Biopsy Bottle No 4
- 3206Small Biopsy Bottle No 7
- 3207Small Biopsy Bottle No 5
- 3209Solid Tumor Combo1 [EGFR, ALK1, ROS1, MET, PDL1]
- 3211Solid Tumor Combo2 [MSI, NRAS, KRAS, BRAF, H RAS]
- 3217Small Biopsy Bottle No 8
- 3220Targeted Mutation Analysis (2 Mutations)
- 3221TEL/AML (ALL)
- 3222TBX5 Full Length Gene Sequence Analysis (Holt-Oram Syndrome)
- 3223TEL/AML1 Qualitative
- 3226Trisomy 8 (AML)
- 3234William's Syndrome (FISH)
- 3235Trisomy 12 (CLL)
- 3238X & Y [Sex Mismatch Bone Marrow Transplant]
- 3248ABL Gene Load Test
- 3250Adenovirus + Boca Virus + Metapneumonia + RSV Detection and Differentiation (RNA Detection) Qualitative Test
- 3258B. Pseudomalie (RNA Detection) Qualitative Test
- 3264Boca Virus Viral Load Quantitative Test
- 3266Bordetella Pertussis Bacterial Load Test
- 3271CCHF (Crimean Congo Hemorrhagic Fever) Viral Load Quantitative Test
- 3274Chandipora Virus Viral Load Quantitative Test
- 3281CMV (RNA Detection) Qualitative Test
- 3287Chlamydia trachomatis, N. gonorrhoea, M. genitalium Multiplex Detection & Differentiation (RNA Detection) Qualitative Test
- 3288CML MRD1 Viral Load Quantitative Test
- 3289CCL3-L1 Gene Load Test
- 3292Cryptococcus (RNA Detection) Qualitative Test
- 3307Filaria Bacterial Load Test
- 3310Filaria (RNA Detection) Qualitative Test
- 3314Filaria Multiplex (Brugia timori, Brugia pahangi, Brugia malayi, and Wuchereria bancrofti) Detection & Differentiation (RNA Detection) Qualitative Test
- 3318HCV Genotyping 1/2/3/4 (RNA Detection) Qualitative Test
- 3325Human Papillomavirus 16 & 18 (HPV) (RNA Detection) Qualitative Test
- 3329HHV 7 Viral Load Quantitative Test
- 3331HHV 7 (DNA Detection) (RNA Detection) Qualitative Test
- 3332H5N1 (Bird Flu) Test
- 3357Shrimp WSSV, MBV, HPV, IHHNV DNA Virus Multiplex Detection and Differentiation (RNA Detection) Qualitative Test
- 3363Staph Aureus (RNA Detection) Qualitative Test
- 3368Fish Species Authentication
- 3369Meat Species Authentication
- 3388Mastitis Partial Panel Without
- 33987 Kb Matepair Library Preparation
- 3399Genotyping by Sequencing-96 Samples
- 3400ChIP Sequencing
- 3413Eukaryotic Stranded mRNA Sequencing
- 3420Eukaryotic SmallRNA Sequencing
- 3427Eukaryotic mRNA Sequencing-Low Input
- 3428Eukaryotic Stranded mRNA Library Preparation
- 3433Eukaryotic SmallRNA Library Preparation
- 3440Comprehensive Tumor Panel (SNVs, Small Indels, Fusions) + TMB + MSI (526 Genes)
- 3441Nipah Virus Qualitative PCR Test
- 3447Fecal Immunochemical Test
- 3448HIV Rapid Blood Test 4th Generation Price
- 3453Anemia Panel 2 Test
- 3454Calcitonin Stimulation by Calcium-Pentagastrin Test
- 3458Cryoglobulins Panel Test
- 3462Chronic Lymphocytic Leukemia (CLL) Prognostic Panel Test
- 3463CSF Leakage Evaluation (Nasal/Ear Discharge) Test
- 3466Antenatal Panel Basic Test
- 3467Cytology (Pap Smear) Genital Female Conventional Test
- 3472FISH - Follicular Lymphoma (IGH/BCL2) t(14;18) Test
- 3476Hair Transplant Panel B with COVID Antibodies Test
- 3481HLA DNA Typing for Kidney / Liver Transplant PCR Test
- 3486Immune Deficiency Panel 2 Test
- 3488Immunophenotyping by Flow Cytometry CD MPO Test
- 3489Immunophenotyping by Flow Cytometry Kappa & Lambda Light Chains Test
- 3490Immunophenotyping by Flow Cytometry CD14 Test
- 3492Immunophenotyping by Flow Cytometry CD22 Test
- 3493Immunophenotyping by Flow Cytometry CD20 Test
- 3494Immunophenotyping by Flow Cytometry CD79a Test
- 3495Immunophenotyping by Flow Cytometry CD7 Test
- 3496Immunophenotyping by Flow Cytometry IgG Heavy Chain Cytoplasmic Test
- 3497Immunophenotyping by Flow Cytometry IgM Heavy Chain Cytoplasmic Test
- 3498Immunophenotyping by Flow Cytometry ZAP-70 Test
- 3499Immunophenotyping by Flow Cytometry TdT Test
- 3500Immunophenotyping by Flow Cytometry: Leukemia Diagnostic Comprehensive Profile Any 6 Markers Test
- 3501Immunophenotyping by Flow Cytometry: Leukemia Diagnostic Panel Customized Any 10 Markers Test
- 3503Immunophenotyping by Flow Cytometry: Leukemia Diagnostic Panel-AML Characterization Test
- 3504Immunophenotyping by Flow Cytometry: Leukemia / Lymphoma Diagnostic Panel-Chronic Lymphoproliferative Disorders T & B Cell Test
- 3510Expert Breast Cancer Panel Test
- 3527Paroxysmal Nocturnal Hemoglobinuria (PNH) Confirmatory Test Test
- 3539Pernicious Anemia Panel Test
- 3546Pheochromocytoma Profile Test
- 3559PML RARA t(1517)(q22q12) Gene Rearrangement Quantitative MRD Monitor Test
- 3563Plasminogen Activator Inhibitor-1 (PAI-1) Test
- 3568Pompe Disease Quantitative Blood Test
- 3572Prader-Willi Syndrome Mutation Detection Methylation Specific PCR Test
- 3573Protein - Creatinine Ratio Urine Test
- 3575Prenatal Diagnosis Panel 2 Amniotic Fluid Test
- 3576Protein S Functional / Activity Test
- 3578PSA (Prostate-Specific Antigen) Total Test
- 3579Prothrombin Gene Mutation Analysis Test
- 3580PSA Profile Test
- 3581PSA (Prostate-Specific Antigen) Free Test
- 3585Protein Electrophoresis 24 Hour Urine Test
- 3603Respiratory Syncytial Virus (RSV) Antigen Test
- 3605Rheumatoid Autoimmune Panel Test
- 3612Rotavirus Antigen Stool Test
- 3613ROMA Risk of Ovarian Malignancy Algorithm Test
- 3621Rubella Detection PCR Test
- 3625SARS-CoV-2 Monitoring Panel Test
- 3635Sickle Cell Anemia Mutation Detection Test
- 3641Serotonin (5-HT) Serum Test
- 3650Soluble Transferrin Receptor (sTfR) Serum Test
- 3656Sphingolipidosis Panel 1 Test
- 3661Spino-Bulbar Muscular Atrophy Test
- 3663Steroid Panel 1:6 Steroids Test
- 3668Stomach Health Test / Gastro Panel Test
- 3677TB Gold Plus Interferon Gamma Release Assay (IGRA) Test
- 3690Thalassemia Monitoring Panel Test
- 3692Thrombophilia Comprehensive Profile Test
- 3694Thyroglobulin Tg Test
- 3695Thrombophilia Profile Test
- 3698Topiramate Test
- 3699Tissue Transglutaminase TTG-DGP Screen Test
- 3706Toxoplasma Antibodies Panel IgG & IgM Test
- 3708TSH Receptor Antibody Test
- 3717UGT1A1 Gene Polymorphism (Nucleotide 'TA' Repeats) Detection Test
- 3721Vancomycin Test
- 3734Vitamin B6 Pyridoxine Test
- 3743Vitamin D Comprehensive Test
- 3747Vitamin Screen Test
- 3749Vitamin B1 Thiamine Test
- 3751Von Willebrand Factor Antigen vWF Ag Test
- 3752Von Willebrand Factor Collagen Binding Activity (vWF) Test
- 3753Von Willebrand Disease (VWD) Panel Test
- 3759VMA (Vanillyl Mandelic Acid) Random Urine Test
- 3760Warfarin Sensitivity Detection Test
- 3770BEST1 Gene Bestrophinopathy NGS Genetic Test
- 3791LIM2 Gene Cataract, Cortical Pulverulent, Late-Onset NGS Genetic Test
- 3793CRYAB Gene Cataract, Posterior Polar Type 2 NGS Genetic Test
- 3794SIL1 Gene Cataract, Congenital, Associated with Marinesco-Sjogren Syndrome NGS Genetic Test
- 3801PRPH2 Gene Choroidal Dystrophy, Central Areolar Type 2 NGS Genetic Test
- 3840HPS3 Gene Hermansky-Pudlak Syndrome Type 3 NGS Genetic Test
- 3842Amyotrophic Lateral Sclerosis (ALS) Panel NGS Genetic Test
- 3866APP Gene Alzheimer Disease Type 1 NGS Genetic Test
- 3872SORL1 Gene Alzheimers Disease, Early Onset, Autosomal Dominant NGS Genetic Test
- 3896C9orf72 Gene Amyotrophic Lateral Sclerosis with Frontotemporal Dementia NGS Genetic Test
- 3903MYO16 Gene Autism Spectrum, MYO16 Related NGS Genetic Test
- 3906NLGN3 Gene Autism Susceptibility, X-Linked Type 1 NGS Genetic Test
- 3910RPL10 Gene Autism Susceptibility, X-Linked Type 5 NGS Genetic Test
- 3936COL6A3 Gene Bethlem Myopathy Type 1 NGS Genetic Test
- 3939PHF6 Gene Borjeson-Forssman-Lehmann Syndrome NGS Genetic Test
- 3947APP Gene Cerebral Amyloid Angiopathy, APP Related NGS Genetic Test
- 3964NDRG1 Gene CMT4D NGS Genetic Test
- 3966CTDP1 Gene CMT4, CTDP1 Related NGS Genetic Test
- 3985SLC6A8 Gene Creatine deficiency syndrome X-linked NGS Genetic Test
- 4004GNAQ Gene Developmental delay, GNAQ related NGS Genetic Test
- 4008ATN1 Gene Dentatorubral-pallidoluysian atrophy NGS Genetic Test
- 4015HSPG2 Gene Dyssegmental dysplasia, Silverman-Handmaker type NGS Genetic Test
- 4016ADCY5 Gene Dyskinesia, familial, with facial myokymia NGS Genetic Test
- 4019PDE10A Gene Dyskinesia, limb and orofacial, infantile-onset NGS Genetic Test
- 4025ARX Gene Early infantile epileptic encephalopathy type 1 NGS Genetic Test
- 4046ARHGEF9 Gene Early infantile epileptic encephalopathy type 8 NGS Genetic Test
- 4066CACNA1H Gene Epilepsy, childhood absence type 6, susceptibility to NGS Genetic Test
- 4072DEPDC5 Gene Epilepsy, familial focal with variable foci NGS Genetic Test
- 4074SCN3A Gene Epilepsy, focal, SCN3A related NGS Genetic Test
- 4083SCARB2 Gene Epilepsy, progressive myoclonic type 4, with or without renal failure NGS Genetic Test
- 4093SLC1A3 Gene Episodic ataxia type 6 NGS Genetic Test
- 4131HTT Gene Huntington disease NGS Genetic Test
- 4132ZDHHC17 Gene Huntington disease, ZDHHC17 related NGS Genetic Test
- 4137NGF Gene HSAN5 NGS Genetic Test
- 4158RYR1 Gene King-Denborough syndrome NGS Genetic Test
- 4166COX15 Gene Leigh syndrome NGS Genetic Test
- 4183MT-ND6 Gene Leigh syndrome due to mitochondrial complex I deficiency NGS Genetic Test
- 4205TTN Gene Limb-girdle muscular dystrophy, autosomal recessive type 2J NGS Genetic Test
- 4216MT-TL1 Gene MELAS syndrome, MT-TL1 related NGS Genetic Test
- 4233PACS1 Gene Mental retardation, autosomal dominant type 17 NGS Genetic Test
- 4238DEAF1 Gene Mental retardation, autosomal dominant type 24 NGS Genetic Test
- 4242AHDC1 Gene Mental retardation, autosomal dominant type 25 NGS Genetic Test
- 4249GRIN2B Gene Mental retardation, autosomal dominant type 6 NGS Genetic Test
- 4273NSUN2 Gene Mental retardation, autosomal recessive type 5 NGS Genetic Test
- 4301MT-ND2 Gene Mitochondrial complex I deficiency NGS Genetic Test
- 4303NDUFA11 Gene Mitochondrial complex I deficiency NGS Genetic Test
- 4323SUCLA2 Gene Mitochondrial DNA depletion syndrome NGS Genetic Test
- 4349FKRP Gene Muscular dystrophy type 1C NGS Genetic Test
- 4353LAMA2 Gene Muscular dystrophy type 1A NGS Genetic Test
- 4366MUSK Gene Myasthenic syndrome associated with acetylcholine receptor deficiency NGS Genetic Test
- 4388CRYAB Gene Myopathy, myofibrillar, fatal infantile hypertrophy, alpha-B crystallin-related NGS Genetic Test
- 4396MTM1 Gene Myotubular myopathy X-linked NGS Genetic Test
- 4412CTNNA2 Gene Neuronal migration disorder NGS Genetic Test
- 4420HSPB1 Gene Neuronopathy distal hereditary motor type 2B NGS Genetic Test
- 4424BSCL2 Gene Neuropathy, distal hereditary motor, type 5A NGS Genetic Test
- 4435SCN9A Gene Neuropathy, hereditary sensory and autonomic type 2 NGS Genetic Test
- 4455PEX5 Gene Peroxisome biogenesis disorder type 2B NGS Genetic Test
- 4469GAA Gene Pompe disease NGS Genetic Test
- 4482AMPD2 Gene Pontocerebellar hypoplasia, type 9 NGS Genetic Test
- 4487POLG Gene Progressive external ophthalmoplegia with mitochondrial deletions type 1, autosomal dominant NGS Genetic Test
- 4502ALDH3A2 Gene Sjogren-Larsson syndrome NGS Genetic Test
- 4515ULK2 Gene Smith-Magenis syndrome, ULK2 related NGS Genetic Test
- 4526SPG21 Gene SPG21 NGS Genetic Test
- 4527B4GALNT1 Gene SPG26 NGS Genetic Test
- 4531FA2H Gene SPG35 NGS Genetic Test
- 4539AR Gene Spinal and bulbar muscular atrophy X-linked NGS Genetic Test
- 4542PLEKHG5 Gene Spinal muscular atrophy distal, autosomal recessive type 4 NGS Genetic Test
- 4547SMN1 Gene Spinal muscular atrophy type 1 NGS Genetic Test
- 4552SMN1 Gene Spinal muscular atrophy type 2 NGS Genetic Test
- 4553PRKCH Gene Cerebral Infarction, Susceptibility to NGS Genetic Test
- 4554FLNA Gene Heterotopia, periventricular, X-linked dominant NGS Genetic Test
- 4557VGKC (Voltage Gated Potassium Channel) Antibody CSF Test
- 4559ATP7A Gene Spinal muscular atrophy, distal, X-linked NGS Genetic Test
- 4560DNAJB2 Gene Spinal muscular atrophy type 5 NGS Genetic Test
- 4568IFRD1 Gene Spinocerebellar ataxia type 18, autosomal dominant NGS Genetic Test
- 4572NOP56 Gene Spinocerebellar ataxia type 36, autosomal dominant NGS Genetic Test
- 4576CACNA1A Gene Spinocerebellar ataxia type 6, autosomal dominant NGS Genetic Test
- 4578SYNE1 Gene Spinocerebellar ataxia type 8, autosomal recessive NGS Genetic Test
- 4579TDP1 Gene Spinocerebellar ataxia with axonal neuropathy, autosomal recessive NGS Genetic Test
- 4581ATXN8OS Gene Spinocerebellar ataxia type 8, autosomal dominant NGS Genetic Test
- 4582TPP1 Gene Spinocerebellar ataxia type 7, autosomal recessive NGS Genetic Test
- 4583COQ8A Gene Spinocerebellar ataxia type 9, autosomal rececssive NGS Genetic Test
- 4590SLITRK1 Gene Tourette syndrome NGS Genetic Test
- 4596TSC2 Gene Tuberous sclerosis type 2 NGS Genetic Test
- 4599CRB2 Gene Ventriculomegaly with cystic kidney disease NGS Genetic Test
- 4601TTPA Gene Vitamin E familial deficiency NGS Genetic Test
- 4604SNAI2 Gene Waardenburg syndrome type 2D NGS Genetic Test
- 4606FKRP Gene Walker-Warburg syndrome or muscle-eye-brain disease, FKRP related NGS Genetic Test
- 4609RAB3GAP1 Gene Warburg micro syndrome type 1 NGS Genetic Test
- 4614DECR1 Gene 2,4-dienoyl-CoA reductase 1 NGS Genetic Test
- 4615NADK2 Gene 2,4-dienoyl-CoA reductase deficiency NGS Genetic Test
- 4620HIBCH Gene 3-hydroxyisobutryl-CoA hydrolase deficiency NGS Genetic Test
- 4622HMGCS2 Gene 3-hydroxy-3-methylglutaryl-CoA synthase 2 deficiency NGS Genetic Test
- 4636ASNS Gene Asparaginesynthetase deficiency NGS Genetic Test
- 4642UPB1 Gene Beta-ureidopropionase deficiency NGS Genetic Test
- 4647AKR1D1 Gene Bile acid synthesis defect type 2, congenital NGS Genetic Test
- 4651COQ6 Gene Coenzyme Q10 deficiency type 6 NGS Genetic Test
- 4655ACSF3 Gene Combined malonic and methylmalonic aciduria NGS Genetic Test
- 4656TARS2 Gene Combined oxidative phosphorylation deficiency type 21 NGS Genetic Test
- 4660CFTR Gene Cystic fibrosis NGS Genetic Test
- 4667HNF1A Gene Diabetes mellitus, insulin-dependent type 20 NGS Genetic Test
- 4670AKT2 Gene Diabetes mellitus, noninsulin-dependent NGS Genetic Test
- 4674CYP2B6 Gene Efavirenz, poor metabolism of NGS Genetic Test
- 4679FANCF Gene Fanconi anemia type F NGS Genetic Test
- 4681KHK Gene Fructosuria essential NGS Genetic Test
- 4682PSAP Gene Gaucher disease, atypical NGS Genetic Test
- 4685ALG8 Gene Glycosylation disorder type 1H NGS Genetic Test
- 4687ALG12 Gene Glycosylation disorder type 1G NGS Genetic Test
- 4689SLC35A1 Gene Glycosylation disorder type 2F NGS Genetic Test
- 4691COG1 Gene Glycosylation disorder type 2G NGS Genetic Test
- 4693HFE Gene Hemochromatosis classical NGS Genetic Test
- 4694HAMP Gene Hemochromatosis type 2B NGS Genetic Test
- 4695CYP24A1 Gene Hypercalcemia infantile type NGS Genetic Test
- 4697G6PD Gene Hemolytic anemia due to G6PD deficiency NGS Genetic Test
- 4698SLC40A1 Gene Hemochromatosis type 4 NGS Genetic Test
- 4704LDLRAP1 Gene Hypercholesterolemia autosomal recessive NGS Genetic Test
- 4705APOB Gene Hypobetalipoproteinemia type 1 NGS Genetic Test
- 4706PCBD1 Gene Hyperphenylalaninemia, BH4 deficient, type D NGS Genetic Test
- 4714ACAD8 Gene Isobutyryl-CoA dehydrogenase deficiency NGS Genetic Test
- 4717PSAP Gene Krabbe disease, atypical NGS Genetic Test
- 4722AGPAT2 Gene Lipodystrophy generalized type 1 NGS Genetic Test
- 4725LMBRD1 Gene Methylmalonic aciduria CblF type NGS Genetic Test
- 4728MPC1 Gene Mitochondrial pyruvate carrier deficiency NGS Genetic Test
- 4729GNPTAB Gene Mucolipidosis type 2 alpha/beta NGS Genetic Test
- 4730GNPTAB Gene Mucolipidosis type 3 NGS Genetic Test
- 4734ILDR1 Gene Deafness, autosomal recessive type 42 NGS Genetic Test
- 4736CIB2 Gene Deafness, autosomal recessive type 48 NGS Genetic Test
- 4740SLC26A5 Gene Deafness, autosomal recessive type 61 NGS Genetic Test
- 4742LRTOMT Gene Deafness, autosomal recessive type 63 NGS Genetic Test
- 4752TBC1D24 Gene Deafness, autosomal recessive type 86 NGS Genetic Test
- 4761POU3F4 Gene Deafness, X-linked type 2 NGS Genetic Test
- 4772CCDC103 Gene Primary ciliary dyskinesia type 17 NGS Genetic Test
- 4774DNAAF3 Gene Primary ciliary dyskinesia type 2 NGS Genetic Test
- 4780DYX1C1 Gene Primary ciliary dyskinesia type 25 NGS Genetic Test
- 4782SPAG1 Gene Primary ciliary dyskinesia type 28 NGS Genetic Test
- 4785CCNO Gene Primary ciliary dyskinesia type 29 NGS Genetic Test
- 4800MASP1 Gene 3MC syndrome type 1 NGS Genetic Test
- 4808PSEN1 Gene Acne inversa familial type 3 NGS Genetic Test
- 4810PDE4D Gene Acrodysostosis 2 NGS Genetic Test
- 4814ARHGAP31 Gene Adams-Oliver syndrome type 1 NGS Genetic Test
- 4826ENAM Gene Amelogenesis imperfecta type 1B NGS Genetic Test
- 4830AMBN Gene Amelogenesis imperfecta type 1F NGS Genetic Test
- 4832ITGB6 Gene Amelogenesis imperfecta type 1H NGS Genetic Test
- 4837FAM83H Gene Amelogenesis imperfecta type 3 NGS Genetic Test
- 4845MYH3 Gene Arthrogryposis, distal, type 2B NGS Genetic Test
- 4852CARD11 Gene B-cell expansion with NFKB and T-cell anergy NGS Genetic Test
- 4854RFXANK Gene Bare lymphocyte syndrome, type 2 NGS Genetic Test
- 4855FGFR2 Gene Beare-Stevenson cutis gyrata syndrome NGS Genetic Test
- 4859PLS3 Gene Bone mineral density QTL18, osteoporosis NGS Genetic Test
- 4878EFEMP2 Gene Cutis laxa type 1B, autosomal recessive NGS Genetic Test
- 4879FBLN5 Gene Cutis laxa type 2, autosomal dominant NGS Genetic Test
- 4880PYCR1 Gene Cutis laxa type 2B, autosomal recessive NGS Genetic Test
- 4881ATP6V0A2 Gene Cutis laxa type 2A, autosomal recessive NGS Genetic Test
- 4888DSPP Gene Dentinogenesis imperfecta, Shields type 3 NGS Genetic Test
- 4889KRT14 Gene Dermatopathia pigmentosa reticularis NGS Genetic Test
- 4890MTAP Gene Diaphyseal medullary stenosis with malignant fibrous histiocytoma NGS Genetic Test
- 4894TERT Gene Dyskeratosis congenita, autosomal recessive type 4/ autosomal dominant type 2 NGS Genetic Test
- 4896NHP2 Gene Dyskeratosis congenita, autosomal recessive type 2 NGS Genetic Test
- 4897RTEL1 Gene Dyskeratosis congenita, autosomal recessive type 5 NGS Genetic Test
- 4901DKC1 Gene Dyskeratosis congenita, X-linked NGS Genetic Test
- 4903CDH3 Gene Ectodermal dysplasia, ectrodactyly, and macular dystrophy NGS Genetic Test
- 4906EDAR Gene Ectodermal dysplasia, hypohidrotic, autosomal recessive NGS Genetic Test
- 4907EDARADD Gene Ectodermal dysplasia, hypohidrotic, autosomal recessive NGS Genetic Test
- 4912COL5A2 Gene Ehlers-Danlos syndrome type 1/2 NGS Genetic Test
- 4915PKP1 Gene Ectodermal dysplasia/skin fragility syndrome NGS Genetic Test
- 4916PLOD1 Gene Ehlers-Danlos syndrome type 6 NGS Genetic Test
- 4919COL1A1 Gene Ehlers-Danlos syndrome type 7A NGS Genetic Test
- 4924GATA2 Gene Emberger syndrome NGS Genetic Test
- 4929GJB4 Gene Erythrokeratodermia variabilis et progressive NGS Genetic Test
- 4931MIR17HG Gene Feingold syndrome type 2 NGS Genetic Test
- 4942ANO5 Gene Gnathodiaphyseal dysplasia NGS Genetic Test
- 4945CYBA Gene Granulomatous disease, chronic, autosomal recessive, cytochrome b-negative NGS Genetic Test
- 4946GORAB Gene Geroderma osteodysplasticum NGS Genetic Test
- 4948NCF4 Gene Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 3 NGS Genetic Test
- 4953MYO5A Gene Griscelli syndrome type 1 NGS Genetic Test
- 4955CTSC Gene Haim-Munk syndrome NGS Genetic Test
- 4965TLR3 Gene Herpes simplex encephalitis type 2, susceptibility to NGS Genetic Test
- 4967ANTXR2 Gene Hyaline fibromatosis syndrome NGS Genetic Test
- 4968DOCK8 Gene Hyper-IgE recurrent infection syndrome, autosomal recessive NGS Genetic Test
- 4969HPGD Gene Hypertrophic osteoarthropathy type 1 NGS Genetic Test
- 4970SLCO2A1 Gene Hypertrophic osteoarthropathy type 2 NGS Genetic Test
- 4973FGF23 Gene Hypophosphatemic rickets, autosomal dominant NGS Genetic Test
- 4986LPAR6 Gene Hypotrichosis type 8 NGS Genetic Test
- 4994MBTPS2 Gene Ichthyosis follicularis, atricia, and photophobia syndrome NGS Genetic Test
- 5000STIM1 Gene Immunodeficiency type 10 NGS Genetic Test
- 5005MALT1 Gene Immunodeficiency type 12 NGS Genetic Test
- 5006CD3D Gene Immunodeficiency type 19 NGS Genetic Test
- 5009AICDA Gene Immunodeficiency type 2, with hyper-IgM NGS Genetic Test
- 5011CD247 Gene Immunodeficiency type 25 NGS Genetic Test
- 5018ISG15 Gene Immunodeficiency type 38 NGS Genetic Test
- 5031ABCB1 Gene Inflammatory bowel disease type 13 NGS Genetic Test
- 5033IL12A Gene Interleukin 12A deficiency NGS Genetic Test
- 5040POMP Gene Keratosis linearis with ichthyosis congenita and sclerosing keratoderma NGS Genetic Test
- 5043FBLIM1 Gene Kindler syndrome NGS Genetic Test
- 5049FERMT3 Gene Leukocyte adhesion deficiency type 3 NGS Genetic Test
- 5051LIG4 Gene LIG4 syndrome NGS Genetic Test
- 5053MR1 Gene Major histocompatibility comples 1 deficiency NGS Genetic Test
- 5064SPRED1 Gene Neurofibromatosis type 1 -like syndrome NGS Genetic Test
- 5072TRPV3 Gene Olmsted syndrome NGS Genetic Test
- 5077DCLRE1C Gene Omenn syndrome NGS Genetic Test
- 5081GNAS Gene Osseous heteroplasia, progressive NGS Genetic Test
- 5082COL1A1 Gene Osteogenesis imperfecta NGS Genetic Test
- 5085COL1A2 Gene Osteogenesis imperfecta NGS Genetic Test
- 5087FKBP10 Gene Osteogenesis imperfecta type 11 NGS Genetic Test
- 5089BMP1 Gene Osteogenesis imperfecta type 13 NGS Genetic Test
- 5090IFITM5 Gene Osteogenesis imperfecta type 5 NGS Genetic Test
- 5093SERPINF1 Gene Osteogenesis imperfecta type 6 NGS Genetic Test
- 5094TNFRSF11A Gene Osteopetrosis, autosomal recessive type 7 NGS Genetic Test
- 5098KRT6A Gene Pachyonychia congenita type 3 NGS Genetic Test
- 5100TNFRSF11B Gene Paget disease, juvenile NGS Genetic Test
- 5101KRT6B Gene Pachyonychia congenita type 4 NGS Genetic Test
- 5104CDSN Gene Peeling skin syndrome type 1 NGS Genetic Test
- 5105CTSC Gene Papillon-Lefevre syndrome NGS Genetic Test
- 5108CAST Gene Peeling skin with leukonychia, acral punctate keratoses, cheilitis, and knuckle pads NGS Genetic Test
- 5109KIT Gene Piebaldism NGS Genetic Test
- 5115GGCX Gene Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency NGS Genetic Test
- 5121CARD14 Gene Psoriasis type 2 NGS Genetic Test
- 5122IL36RN Gene Psoriasis, generalized pustular NGS Genetic Test
- 5126PSTPIP1 Gene Pyogenic sterile arthritis, pyoderma gangrenosum, and acne NGS Genetic Test
- 5139MATN3 Gene Spondyloepimetaphyseal dysplasia, MATN3 related NGS Genetic Test
- 5144ITGAM Gene Systemic lupus erythematosus, susceptibility to NGS Genetic Test
- 5154TTC37 Gene Trichohepatoenteric syndrome type 1 NGS Genetic Test
- 5160RHBDF2 Gene Tylosis with esophageal cancer NGS Genetic Test
- 5161UVSSA Gene UV-sensitive syndrome type 3 NGS Genetic Test
- 5163SOST Gene Van Buchem disease NGS Genetic Test
- 5164TMEM173 Gene Vasculopathy, infantile-onset, TMEM173/STING related NGS Genetic Test
- 5165LORICRIN Gene Vohwinkel syndrome with ichthyosis NGS Genetic Test
- 5176ERCC4 Gene Xeroderma pigmentosum, group F NGS Genetic Test
- 5178XPC Gene Xeroderma pigmentosum, group C NGS Genetic Test
- 5179ERCC5 Gene Xeroderma pigmentosum, group G NGS Genetic Test
- 5191KCNE3 Gene Brugada syndrome type 6 NGS Genetic Test
- 5197HCN4 Gene Brugada syndrome type 8 NGS Genetic Test
- 5199MYBPC3 Gene Cardiomyopathy, dilated NGS Genetic Test
- 5200DSG2 Gene Cardiomyopathy, dilated type 1BB NGS Genetic Test
- 5201RBM20 Gene Cardiomyopathy, dilated type 1DD NGS Genetic Test
- 5202ACTN2 Gene Cardiomyopathy, dilated type 1AA NGS Genetic Test
- 5204TNNT2 Gene Cardiomyopathy, dilated type 1D NGS Genetic Test
- 5205LDB3 Gene Cardiomyopathy, dilated type 1C NGS Genetic Test
- 5206CRYAB Gene Cardiomyopathy, dilated type 1 NGS Genetic Test
- 5208LMNA Gene Cardiomyopathy, dilated type 1A NGS Genetic Test
- 5209MYH6 Gene Cardiomyopathy, dilated type 1EE NGS Genetic Test
- 5212EYA4 Gene Cardiomyopathy, dilated type 1J NGS Genetic Test
- 5215MYPN Gene Cardiomyopathy, dilated type 1KK NGS Genetic Test
- 5217CSRP3 Gene Cardiomyopathy, dilated type 1M NGS Genetic Test
- 5221ACTC1 Gene Cardiomyopathy, dilated type 1R NGS Genetic Test
- 5223PSEN1 Gene Cardiomyopathy, dilated type 1U NGS Genetic Test
- 5224TMPO Gene Cardiomyopathy, dilated type 1T NGS Genetic Test
- 5226VCL Gene Cardiomyopathy, dilated type 1W NGS Genetic Test
- 5229TNNC1 Gene Cardiomyopathy, dilated type 1Z NGS Genetic Test
- 5230TPM1 Gene Cardiomyopathy, dilated type 1Y NGS Genetic Test
- 5233PRKAG2 Gene Cardiomyopathy, familial hypertrophic type 6 NGS Genetic Test
- 5236TNNI3 Gene Cardiomyopathy, familial restrictive type 1 NGS Genetic Test
- 5239PLN Gene Cardiomyopathy, hypertrophic, type 18 NGS Genetic Test
- 5240MT-TH Gene Cardiomyopathy, idiopathic dilated, mitochondrial, MT-TH related NGS Genetic Test
- 5241PHOX2B Gene Central hypoventilation syndrome with or without Hirschsprung disease NGS Genetic Test
- 5242ASCL1 Gene Central hypoventilation syndrome, congenital NGS Genetic Test
- 5245GATA5 Gene Congenital heart defects multiple types NGS Genetic Test
- 5249ZFPM2 Gene Diaphragmatic hernia type 3 NGS Genetic Test
- 5250MMP3 Gene Coronary heart disease, susceptibility to, type 6 NGS Genetic Test
- 5251DBH Gene Dopamine beta-hydroxylase (DBH) deficiency NGS Genetic Test
- 5253DSP Gene Dilated cardiomyopathy with woolly hair, keratoderma, and tooth agenesis NGS Genetic Test
- 5256SCN5A Gene Heart block, progressive, familial, type 1A NGS Genetic Test
- 5258LMNA Gene Heart-hand syndrome, Slovenian type NGS Genetic Test
- 5260KCNE1 Gene Jervell and Lange-Nielsen syndrome type 2 NGS Genetic Test
- 5265SNTA1 Gene Long QT syndrome type 12 NGS Genetic Test
- 5266AKAP9 Gene Long QT syndrome type 11 NGS Genetic Test
- 5269PUS1 Gene Mitochondrial myopathy and sideroblastic anemia type 1 NGS Genetic Test
- 5270MT-TS2 Gene MERRF/MELAS overlap syndrome, MT-TS2 related NGS Genetic Test
- 5275MT-TA Gene Mitochondrial myopathy, MT-TA related NGS Genetic Test
- 5277ACTA2 Gene Moyamoya disease type 5 NGS Genetic Test
- 5278MT-TQ Gene Myopathy, MT-TQ related NGS Genetic Test
- 5281SFTPA1 Gene Pulmonary fibrosis, idiopathic NGS Genetic Test
- 5283AGK Gene Sengers syndrome NGS Genetic Test
- 5286EIF2AK4 Gene Pulmonary venoocclusive disease type 2 NGS Genetic Test
- 5291SCN5A Gene Sudden infant death syndrome, susceptibility to NGS Genetic Test
- 5293GATA6 Gene Tetralogy of Fallot NGS Genetic Test
- 5300CITED2 Gene Ventricular septal defect type 2 NGS Genetic Test
- 5310GP1BA Gene Bernard Soulier syndrome type A2 NGS Genetic Test
- 5311NOTCH3 Gene CADASIL NGS Genetic Test
- 5318F2 Gene Factor II deficiency NGS Genetic Test
- 5321F7 Gene Factor VII deficiency NGS Genetic Test
- 5333TGFB2 Gene Loeys-Dietz syndrome type 4 NGS Genetic Test
- 5335GUCY1A3 Gene Moyamoya type 6 with achalasia NGS Genetic Test
- 5337SERPINE1 Gene Plasminogen activator inhibitor type 1 NGS Genetic Test
- 5346BMPR2 Gene Pulmonary hypertension, primary type NGS Genetic Test
- 5352ELN Gene Supravalvar aortic stenosis NGS Genetic Test
- 5353CALCRL Gene Vascular system defects due to CALCRL deficiency NGS Genetic Test
- 5360TBX19 Gene Adrenocorticotropic hormone deficiency NGS Genetic Test
- 5366AR Gene Androgen insensitivity, partial, with or without breast cancer NGS Genetic Test
- 5376WDPCP Gene Bardet-Biedl syndrome type 15 NGS Genetic Test
- 5377BBS4 Gene Bardet-Biedl syndrome type 4 NGS Genetic Test
- 5380BBS7 Gene Bardet-Biedl syndrome type 7 NGS Genetic Test
- 5385SLC2A2 Gene Fanconi-Bickel syndrome NGS Genetic Test
- 5388TRPC6 Gene Focal segmental glomerulosclerosis type 2 NGS Genetic Test
- 5391MYO1E Gene Focal segmental glomerulosclerosis type 6 NGS Genetic Test
- 5398SLC12A3 Gene Gitelman syndrome NGS Genetic Test
- 5406GLDC Gene Glycine encephalopathy NGS Genetic Test
- 5411CFHR1 Gene Hemolytic uremic syndrome NGS Genetic Test
- 5413CFHR2 Gene Hemolytic uremic syndrome NGS Genetic Test
- 5414CFHR3 Gene Hemolytic uremic syndrome NGS Genetic Test
- 5416CFHR5 Gene Hemolytic uremic syndrome NGS Genetic Test
- 5426SLCO1B3 Gene Hyperbilirubinemia, Rotor type NGS Genetic Test
- 5449MKKS Gene McKusick-Kaufman syndrome NGS Genetic Test
- 5450B9D2 Gene Meckel syndrome type 10 NGS Genetic Test
- 5458MEN1 Gene Multiple endocrine neoplasia type 1 NGS Genetic Test
- 5459CLCN5 Gene Nephrolithiasis type 1 NGS Genetic Test
- 5462TTC21B Gene Nephronophthisis type 12 NGS Genetic Test
- 5464ZNF423 Gene Nephronophthisis type 14 NGS Genetic Test
- 5465WDR19 Gene Nephronophthisis type 13 NGS Genetic Test
- 5467CEP164 Gene Nephronophthisis type 15 NGS Genetic Test
- 5479SLC26A4 Gene Pendred syndrome NGS Genetic Test
- 5484PKHD1 Gene Polycystic kidney and hepatic disease NGS Genetic Test
- 5489PKD1 Gene Polycystic kidney disease type 1, autosomal dominant NGS Genetic Test
- 5491SULT2A1 Gene Polycystic ovary syndrome type 1 NGS Genetic Test
- 5496NR3C2 Gene Pseudohypoaldosteronism, type 1, autosomal dominant NGS Genetic Test
- 5497WNK4 Gene Pseudohypoaldosteronism, type 2B NGS Genetic Test
- 5500GNAS Gene Pseudopseudohypoparathyroidism NGS Genetic Test
- 5501GNAS Gene Pseudohypoparathyroidism type 1A NGS Genetic Test
- 5503SCNN1G Gene Pseudohypoaldosteronism, type 1, autosomal recessive NGS Genetic Test
- 5507ACE Gene Renal tubular dysgenesis NGS Genetic Test
- 5510ATP6V0A4 Gene Renal tubular acidosis, distal, autosomal recessive NGS Genetic Test
- 5514SOX17 Gene Vesicoureteral reflux type 3 NGS Genetic Test
- 5517Infertility panel NGS Genetic Test
- 5519AKR1C4 Gene 46,XY sex reversal type 8, modifier of NGS Genetic Test
- 5526FOXF2 Gene Disorders of sex development with cleft palate NGS Genetic Test
- 5532KHDC3L Gene Hydatidiform mole, recurrent, type 2 NGS Genetic Test
- 5556Blood coagulation panel NGS Genetic Test
- 5560FGB Gene Afibrinogenemia, congenital NGS Genetic Test
- 5574GLRX5 Gene Anemia, sideroblastic, pyridoxine-refractory, autosomal recessive NGS Genetic Test
- 5577GATA1 Gene Anemia, X-linked NGS Genetic Test
- 5579ALAS2 Gene Anemia, sideroblastic, X-linked NGS Genetic Test
- 5583CYBB Gene Granulomatous disease, chronic, X-linked NGS Genetic Test
- 5588CD59 Gene Hemolytic anemia, CD59-mediated, with or without immune-mediated polyneuropathy NGS Genetic Test
- 5598ITK Gene Lymphoproliferative syndrome type 1 NGS Genetic Test
- 5599CTLA4 Gene Lymphoproliferative syndrome, autoimmune, type 5 NGS Genetic Test
- 5601SH2D1A Gene Lymphoproliferative syndrome, X-linked type 1 NGS Genetic Test
- 5606PDGFRB Gene Myeloproliferative disorder, chronic, with eosinophilia NGS Genetic Test
- 5608ELANE Gene Neutropenia, severe congenital type 1 NGS Genetic Test
- 5609VPS45 Gene Neutropenia, severe congenital type 5, autosomal recessive NGS Genetic Test
- 5612RUNX1 Gene Platelet disorder with associated myeloid malignancy NGS Genetic Test
- 5613GGCX Gene Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency NGS Genetic Test
- 5615CD36 Gene Platelet glycoprotein IV deficiency NGS Genetic Test
- 5616SMARCAL1 Gene Schimke immunoosseous dysplasia NGS Genetic Test
- 5618SBDS Gene Shwachman-Diamond syndrome NGS Genetic Test
- 5621HBB Gene Sickle cell anemia NGS Genetic Test
- 5622TRNT1 Gene Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay NGS Genetic Test
- 5623ANK1 Gene Spherocytosis type 1 NGS Genetic Test
- 5625SPTA1 Gene Spherocytosis type 3 NGS Genetic Test
- 5626STIM1 Gene Stormorken syndrome NGS Genetic Test
- 5627EPB42 Gene Spherocytosis type 5 NGS Genetic Test
- 5628HBA1 Gene Thalassemia, alpha NGS Genetic Test
- 5629HBA2 Gene Thalassemia, alpha NGS Genetic Test
- 5631GP1BA Gene von Willebrand disease platelet type NGS Genetic Test
- 5634VWF Gene von Willebrand disease NGS Genetic Test
- 5637COL2A1 Gene Achondrogenesis type 2 NGS Genetic Test
- 5638PRKAR1A Gene Acrodysostosis type 1, with or without hormone resistance NGS Genetic Test
- 5645NOTCH2 Gene Alagille syndrome type 2 NGS Genetic Test
- 5646GMPPA Gene Alacrima, achalasia and mental retardation syndrome NGS Genetic Test
- 5647LARP7 Gene Alazami syndrome NGS Genetic Test
- 5650TP63 Gene Ankyloblepharon-ectodermal defects-cleft lip/palate NGS Genetic Test
- 5651PITX3 Gene Anterior segment mesenchymal dysgenesis NGS Genetic Test
- 5653FGFR2 Gene Antley-Bixler syndrome NGS Genetic Test
- 5655NKX2-5 Gene Atrial septal defect with atrioventricular conduction defects NGS Genetic Test
- 5657PLCB4 Gene Auriculocondylar syndrome type 2 NGS Genetic Test
- 5665PTCH1 Gene Basal cell nevus syndrome NGS Genetic Test
- 5666ACTG1 Gene Baraitser-Winter syndrome type 2 NGS Genetic Test
- 5668SLC20A2 Gene Basal ganglia calcification type 1, ideopathic NGS Genetic Test
- 5670PDGFB Gene Basal ganglia calcification type 5, idiopathic NGS Genetic Test
- 5676BCS1L Gene Bjornstad syndrome NGS Genetic Test
- 5681HOXD13 Gene Brachydactyly type E1 NGS Genetic Test
- 5682HOXD13 Gene Brachydactyly-syndactyly syndrome NGS Genetic Test
- 5685ROR2 Gene Brachydactyly type B1 NGS Genetic Test
- 5687CD96 Gene C syndrome NGS Genetic Test
- 5689PRG4 Gene Camptodactyly-arthropathy-coxa vara-pericarditis syndrome NGS Genetic Test
- 5691IARS2 Gene Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia NGS Genetic Test
- 5693MEGF8 Gene Carpenter syndrome type 2 NGS Genetic Test
- 5699ECE1 Gene Central hypoventilation syndrome, congenital NGS Genetic Test
- 5700GFRA1 Gene Central hypoventilation syndrome, congenital NGS Genetic Test
- 5701GDNF Gene Central hypoventilation syndrome, congenital NGS Genetic Test
- 5705PHOX2A Gene Central hypoventilation syndrome, congenital NGS Genetic Test
- 5707ERCC1 Gene Cerebrooculofacioskeletal syndrome type 4 NGS Genetic Test
- 5709ZEB2 Gene Central hypoventilation syndrome, congenital NGS Genetic Test
- 5710TFAP2B Gene Char syndrome NGS Genetic Test
- 5713CHM Gene Choroideremia NGS Genetic Test
- 5714PIGL Gene CHIME syndrome NGS Genetic Test
- 5715PTH1R Gene Chondrodysplasia, Blomstrand type NGS Genetic Test
- 5716GPSM2 Gene Chudley-McCullough syndrome NGS Genetic Test
- 5718BMPR1B Gene Chrondrodysplasia, acromesomelic, with genital anomalies NGS Genetic Test
- 5727PRKD1 Gene Congenital heart defects and ectodermal dysplasia NGS Genetic Test
- 5728LAMC3 Gene Cortical malformations, occipital NGS Genetic Test
- 5731TBX15 Gene Cousin syndrome NGS Genetic Test
- 5736IFT43 Gene Cranioectodermal dysplasia type 3 NGS Genetic Test
- 5741IL11RA Gene Craniosynostosis and dental anomalies NGS Genetic Test
- 5745FRAS1 Gene Fraser syndrome NGS Genetic Test
- 5750IRX5 Gene Hamamy syndrome NGS Genetic Test
- 5754FGFR1 Gene Hartsfield syndrome NGS Genetic Test
- 5756LMNA Gene Heart-hand syndrome, Slovenian type NGS Genetic Test
- 5758NODAL Gene Heterotaxy, visceral type 5 NGS Genetic Test
- 5760ZIC3 Gene Heterotaxy, visceral type 1 NGS Genetic Test
- 5768NRG1 Gene Hirschsprung disease NGS Genetic Test
- 5771RET Gene Hirschsprung disease NGS Genetic Test
- 5775GDNF Gene Hirschsprung disease, type 3, susceptibility to NGS Genetic Test
- 5776GLI2 Gene Holoprosencephaly-type 9 NGS Genetic Test
- 5777TGIF1 Gene Holoprosencephaly type 4 NGS Genetic Test
- 5779TBX5 Gene Holt-Oram syndrome NGS Genetic Test
- 5780CDON Gene Holoprosencephaly type 11 NGS Genetic Test
- 5785DCAF17 Gene Hypogonadism, alopecia, Diabetes mellitus, mental retardation and extrapyramidal syndrome NGS Genetic Test
- 5786PIGV Gene Hyperphosphatasia with mental retardation syndrome type 1 NGS Genetic Test
- 5788PIGO Gene Hyperphosphatasia with mental retardation syndrome type 2 NGS Genetic Test
- 5789HYLS1 Gene Hydrolethalus syndrome NGS Genetic Test
- 5790ADK Gene Hypermethioninemia due to adenosine kinase deficiency NGS Genetic Test
- 5791PGAP3 Gene Hyperphosphatasia with mental retardation syndrome type 4 NGS Genetic Test
- 5792AHCY Gene Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase NGS Genetic Test
- 5795CDKN1C Gene IMAGE syndrome NGS Genetic Test
- 5796ZBTB24 Gene Immunodeficiency-centromeric instability-facial anomalies syndrome type 2 NGS Genetic Test
- 5797AR Gene Hypospadias type 1, X-linked NGS Genetic Test
- 5800FGFR1 Gene Jackson-Weiss syndrome NGS Genetic Test
- 5801SALL4 Gene IVIC syndrome NGS Genetic Test
- 5802RBBP8 Gene Jawad syndrome NGS Genetic Test
- 5804FGFR2 Gene Jackson-Weiss syndrome NGS Genetic Test
- 5806PROK2 Gene Kallmann syndrome type 4 NGS Genetic Test
- 5808CHD7 Gene Kallmann syndrome type 5 NGS Genetic Test
- 5810paternal UPD chr. 14 Gene Kagami-Ogata syndrome NGS Genetic Test
- 5811MGP Gene Keutel syndrome NGS Genetic Test
- 5812ANKRD11 Gene KBG syndrome NGS Genetic Test
- 5813GDF6 Gene Klippel-Feil syndrome type 1, autosomal dominant NGS Genetic Test
- 5814EHMT1 Gene Kleefstra syndrome NGS Genetic Test
- 5815MEOX1 Gene Klippel-Feil syndrome type 2, autosomal dominant NGS Genetic Test
- 5816FGF10 Gene LADD syndrome NGS Genetic Test
- 5817GDF3 Gene Klippel-Feil syndrome type 3, autosomal dominant NGS Genetic Test
- 5818COL2A1 Gene Kniest dysplasia NGS Genetic Test
- 5820MYO18B Gene Klippel-Feil syndrome type 4, autosomal dominant, with myopathy and facial dysmorphism NGS Genetic Test
- 5821MED12 Gene Lujan-Fryns syndrome NGS Genetic Test
- 5823TRPS1 Gene Langer-Giedion syndrome NGS Genetic Test
- 5827EFTUD2 Gene Mandibulofacial dysostosis with microcephaly NGS Genetic Test
- 5828POLD1 Gene Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome NGS Genetic Test
- 5829FBN1 Gene Marfan lipodystrophy syndrome NGS Genetic Test
- 5830PIEZO2 Gene Marden-Walker syndrome NGS Genetic Test
- 5831RAB3GAP2 Gene Martsolf syndrome NGS Genetic Test
- 5832FBN1 Gene MASS syndrome NGS Genetic Test
- 5834XK Gene McLeod syndrome with or without chronic granulomatous disease NGS Genetic Test
- 5836AKT3 Gene Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome type 2 NGS Genetic Test
- 5837MED13L Gene Mental retardation and distinctive facial features with or without cardiac defects NGS Genetic Test
- 5838CDT1 Gene Meier-Gorlin syndrome type 4 NGS Genetic Test
- 5839PIK3R2 Gene Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome NGS Genetic Test
- 5841HUWE1 Gene Mental retardation, X-linked syndromic, Turner type NGS Genetic Test
- 5842ORC4 Gene Meier-Gorlin syndrome type 2 NGS Genetic Test
- 5843INPP5E Gene Mental retardation, truncal obesity, retinal dystrophy, and micropenis NGS Genetic Test
- 5847WDR62 Gene Microcephaly with cortical malformations, autosomal recessive type 2 NGS Genetic Test
- 5849TUBGCP6 Gene Microcephaly and chorioretinopathy with or without mental retardation NGS Genetic Test
- 5850IER3IP1 Gene Microcephaly with epilepsy and diabetes syndrome NGS Genetic Test
- 5851SLC25A19 Gene Microcephaly, Amish type NGS Genetic Test
- 5852KIF11 Gene Microcephaly with or without chorioretinopathy, Lymphedema, or Mental retardation, MCLMR NGS Genetic Test
- 5854MCPH1 Gene Microcephaly, autosomal recessive type 1 NGS Genetic Test
- 5855PUS1 Gene Mitochondrial myopathy and sideroblastic anemia type 1 NGS Genetic Test
- 5856TRIM37 Gene Mulibrey nanism NGS Genetic Test
- 5857CEP57 Gene Mosaic variegated aneuploidy syndrome type 2 NGS Genetic Test
- 5858B3GAT3 Gene Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects NGS Genetic Test
- 5859PIGN Gene Multiple congenital anomalies-hypotonia-seizures syndrome type 1 NGS Genetic Test
- 5860NALCN Gene Neuroaxonal neurodegeneration, infantile, with facial dysmophism NGS Genetic Test
- 5861STAC3 Gene Native American myopathy NGS Genetic Test
- 5863SMAD4 Gene Myhre syndrome NGS Genetic Test
- 5864SMARCA2 Gene Nicolaides Baraitser syndrome NGS Genetic Test
- 5865NBN Gene Nijmegen breakage syndrome NGS Genetic Test
- 5866PTPN11 Gene Noonan syndrome type 1 NGS Genetic Test
- 5867SHOC2 Gene Noonan syndrom like NGS Genetic Test
- 5869KRAS Gene Noonan syndrome type 3 NGS Genetic Test
- 5871RAF1 Gene Noonan syndrome type 5 NGS Genetic Test
- 5873NRAS Gene Noonan syndrome type 6 NGS Genetic Test
- 5874RIT1 Gene Noonan syndrome type 8 NGS Genetic Test
- 5875NAA10 Gene Ogden syndrome NGS Genetic Test
- 5876CBL Gene Noonan syndrome-like disorder with or without juvenile meylomonocytic leukemia NGS Genetic Test
- 5877GJA1 Gene Oculodentodigital dysplasia NGS Genetic Test
- 5879TRPV3 Gene Olmsted syndrome NGS Genetic Test
- 5880SUMO1 Gene Orofacial cleft type 10 NGS Genetic Test
- 5881MSX1 Gene Orofacial cleft type 5 NGS Genetic Test
- 5883NECTIN1 Gene Orofacial cleft type 7 NGS Genetic Test
- 5885DDX59 Gene Orofaciodigital syndrome type 5 NGS Genetic Test
- 5888FGFR1 Gene Osteoglophonic dysplasia NGS Genetic Test
- 5889EYA1 Gene Otofaciocervical syndrome NGS Genetic Test
- 5890COL11A2 Gene Otospondylomegaepiphyseal dysplasia NGS Genetic Test
- 5891CPLANE1 Gene Orofaciodigital syndrome type 6 NGS Genetic Test
- 5893GLI3 Gene Pallister-Hall syndrome NGS Genetic Test
- 5895MSX2 Gene Parietal foramina type 1 NGS Genetic Test
- 5897DIS3L2 Gene Perlman Syndrome NGS Genetic Test
- 5898LBR Gene Pelger-Huet anomaly NGS Genetic Test
- 5899chr. 22q13.3 Gene Phelan-McDermid syndrome NGS Genetic Test
- 5900FGFR1 Gene Pfeiffer syndrome NGS Genetic Test
- 5902NRXN1 Gene Pitt-Hopkins syndrome NGS Genetic Test
- 5905COL2A1 Gene Platyspondylic skeletal dysplasia, Torrance type NGS Genetic Test
- 5907STRADA Gene Polyhydramnios, megalencephaly, and symptomatic epilepsy NGS Genetic Test
- 5908TUBB2B Gene Polymicrogyria asymmetric NGS Genetic Test
- 5909ADGRG1 Gene Polymicrogyria bilateral frontoparietal NGS Genetic Test
- 5910TUBA8 Gene Polymicrogyria with optic nerve hypoplasia NGS Genetic Test
- 5911NR2E1 Gene Polymicrogyria bilateral occipital NGS Genetic Test
- 5912PI4KA Gene Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis NGS Genetic Test
- 5913RIPK4 Gene Popliteal pterygium syndrome, lethal type NGS Genetic Test
- 5914IRF6 Gene Popliteal pterygium syndrome type 1 NGS Genetic Test
- 5915COL4A1 Gene Porencephaly, familial NGS Genetic Test
- 5916SOST Gene Sclerosteosis type 1 NGS Genetic Test
- 5917LAMA1 Gene Poretti-Boltshauser syndrome NGS Genetic Test
- 5918ATRIP Gene Seckel syndrome NGS Genetic Test
- 5919CEP152 Gene Seckel syndrome type 5 NGS Genetic Test
- 5924COL2A1 Gene SED congenita NGS Genetic Test
- 5925EXT2 Gene Seizures, scoliosis, and macrocephaly syndrome NGS Genetic Test
- 5926XRCC4 Gene Short stature, microcephaly, and endocrine dysfunction NGS Genetic Test
- 5928NBAS Gene Short stature, optic nerve atrophy, and Pelger-Huet anomaly NGS Genetic Test
- 5930CBFB Gene Skeletal abnormalities, CBFB related NGS Genetic Test
- 5932COL2A1 Gene SMED Strudwick type NGS Genetic Test
- 5934NSD1 Gene Sotos syndrome type 1 NGS Genetic Test
- 5935NFIX Gene Sotos-like syndrome NGS Genetic Test
- 5937DLX5 Gene Split-hand/foot malformation type 1 with sensorineural hearing loss NGS Genetic Test
- 5939WNT10B Gene Split-hand/foot malformation type 6 NGS Genetic Test
- 5941COL2A1 Gene Spondyloperipheral dysplasia NGS Genetic Test
- 5942FBN1 Gene Stiff skin syndrome NGS Genetic Test
- 5944B3GALT6 Gene Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures NGS Genetic Test
- 5945LIFR Gene Stuve-Wiedemann syndrome NGS Genetic Test
- 5947TANC2 Gene TANC2 related brain disorders NGS Genetic Test
- 5948HOXD13 Gene Syndactyly type 5 NGS Genetic Test
- 5949BHLHA9 Gene Syndactyly, mesoaxial synostotic, with phalangeal reduction NGS Genetic Test
- 5950RBM10 Gene Tarp syndrome NGS Genetic Test
- 5951CHSY1 Gene Temtamy preaxial brachydactyly syndrome NGS Genetic Test
- 5955WNT3 Gene Tetraamelia, autosomal recessive NGS Genetic Test
- 5957CCDC8 Gene Three M syndrome type 3 NGS Genetic Test
- 5958FAM58A Gene Toe syndactyly, telecanthus, and anogenital and renal malformations NGS Genetic Test
- 5959PAX9 Gene Tooth agenesis, selective type 3 NGS Genetic Test
- 5960OBSL1 Gene Three M syndrome type 2 NGS Genetic Test
- 5961MSX1 Gene Tooth agenesis, selective type 1 NGS Genetic Test
- 5962GDF1 Gene Transposition of great arteries, dextro-looped 3 NGS Genetic Test
- 5963MED13L Gene Transposition of the great arteries, dextro-looped 1 NGS Genetic Test
- 5964SALL1 Gene Townes-Brocks syndrome NGS Genetic Test
- 5965TCOF1 Gene Treacher Collins syndrome type 1 NGS Genetic Test
- 5967POLR1C Gene Treacher Collins syndrome type 3 NGS Genetic Test
- 5968POLR1D Gene Treacher Collins syndrome type 2 NGS Genetic Test
- 5969HPSE2 Gene Urofacial syndrome type 1 NGS Genetic Test
- 5973IRF6 Gene van der Woude syndrome type 1 NGS Genetic Test
- 5974SCARF2 Gene Van den Ende-Gupta syndrome NGS Genetic Test
- 5975GRHL3 Gene van der Woude syndrome type 2 NGS Genetic Test
- 5976ACTG2 Gene Visceral myopathy NGS Genetic Test
- 5978HOXD13 Gene Vater association NGS Genetic Test
- 5980DDX11 Gene Warsaw breakage syndrome NGS Genetic Test
- 5981RAB3GAP1 Gene Warburg micro syndrome type 1 NGS Genetic Test
- 5982RAB3GAP2 Gene Warburg micro syndrome type 2 NGS Genetic Test
- 5984EZH2 Gene Weaver syndrome NGS Genetic Test
- 5985LTBP2 Gene Weill-Marchesani syndrome type 3 NGS Genetic Test
- 5988KMT2A Gene Wiedemann-Steiner syndrome NGS Genetic Test
- 5989MSX1 Gene Witkop syndrome NGS Genetic Test
- 5990chr. 7q11.23 Gene Williams-Beuren syndrome NGS Genetic Test
- 6000TP53 Gene Li-Fraumeni syndrome type 1 NGS Genetic Test
- 6003RET Gene Multiple endocrine neoplasia type 2A NGS Genetic Test
- 6004CDKN2A Gene Melanoma and neural system tumor syndrome, familial NGS Genetic Test
- 6006EGFR Gene Nonsmall cell lung cancer, familial, susceptibility to NGS Genetic Test
- 6009STK11 Gene Peutz-Jeghers syndrome NGS Genetic Test
- 6015BMPR1A Gene Polyposis syndrome, hereditary mixed type 2 NGS Genetic Test
- 6022CYLD Gene Spiegler-Brooke syndrome NGS Genetic Test
- 6027RHBDF2 Gene Tylosis with esophageal cancer NGS Genetic Test
- 6029AML Panel Deletion/Duplication Detection
- 6030AML FISH PANEL (FISH [AML/ETO, inv(16), PML/RARA, MLL])
- 6031VHL Gene von Hippel-Lindau syndrome NGS Genetic Test
- 6032AML PANEL (Cytogenetics + FISH [AML/ETO, inv(16), PML/RARA, MLL])
- 6033AML PCR Panel (AML/ETO, inv(16), PML/RARA)
- 6034AML1/ETO (AML - M2)
- 6035AML Prognostic Panel (Cytogenetics + PCR) (AML/ETO, INV[16], PML/RARA, FLT3, NPM1, CEBPA)
- 6037Arthrogryposis and Congenital Myasthenic Syndrome Gene Panel
- 6038BCL2
- 6040BCL6
- 6041BCL2/IGH (t14;18)
- 6042FISH: BCL6 (3q27) Gene Rearrangement
- 6043BCR-ABL (CML, AML, ALL)
- 6044BCR-ABL1 Kinase Domain Mutation Analysis [IRMA]
- 6045BCR-ABL Variant Panel_x000D_ Mbcr-b2a2, b3a2, b2a3
- 6046Benign Infantile Epilepsy Gene Panel
- 6048BCR-ABL1 Quantification by DD PCR
- 6051BCR-ABL1 Quantitative (p210,p190,p230)
- 6052Beta Thalassemia-HBB Deletion/Duplication Analysis
- 6056Biopsy Acetylcholinesterase (AChE Stain)
- 6057Beta Thalassemia-HBB Full Gene Analysis (Single)
- 6058Biopsy Breast (Modified Radical Mastectomy)
- 6059Biopsy Electron Microscopy
- 6060Biopsy Breast (Modified Radical Mastectomy+ER+PR)
- 6061Biopsy Breast (Modified Radical Mastectomy) +ER+PR+HER2NEU+KI67)
- 6062Biopsy Kidney with Special Stains and IF
- 6063Biopsy Breast (Modified Radical Mastectomy +ER+PR+HER2NEU)
- 6064Biopsy Muscle with Special Stains & IHC
- 6065Biopsy Liver with Special Stains
- 6067Biopsy Nerve with Special Stains
- 6068Biopsy Renal Transplant with C4D (Without IF)
- 6069Biopsy Skin with IF
- 6070Biopsy Skin
- 6071Biopsy TURP/Prostatic Chips
- 6072Biopsy TURBT/Bladder Tumour
- 6073C-Myc Oncogene
- 6074CLL NGS Panel (FISH +KT + IGVH Mutation Analysis+ NGS TP53 Mutation Analysis)
- 6075C-Myc (ALL, NHL)
- 6076Cystic Fibrosis Mutation Screening (CFTR - Del 508, G551D/R553X, G542X)
- 6078Colorectal Cancer Panel [NRAS, KRAS, BRAF]
- 6079Cystic Fibrosis: CFTR Full Gene Sequence Analysis
- 6080Del(5q) (MDS)
- 6081Del(7q) (MDS)
- 6082Del[11q(ATM)] (MM, CLL)
- 6083Del[13q] (MM, CLL)
- 6084Delta Beta-Thalassaemia Mutation Screening
- 6085Del[17p(p53)] (MM, CLL)
- 6087Di-George Syndrome (FISH)
- 6088Di-George Syndrome (Karyotyping+FISH)
- 6095E2A (ALL)
- 6097Early Infantile Epileptic Encephalopathy Gene Panel
- 6099Eosinophilic Leukemia Panel (FISH PDGFRA,PDGFRB,FGFR1,C BFB)
- 6100Epidermal Growth Factor Receptor Mutation Analysis (EGFR - Exon 18, 19, 20, 21)
- 6101Frozen-3
- 6104Glioma Panel(MGMT, IDH1&2, FISH 1p19q)
- 6106Glucose-6-Phosphate Dehydrogenase (G6PD) Full-Length Gene Sequence Analysis
- 6109Hemoglobin D Punjab(HbD) Mutation Study
- 6110Hereditary Spastic Paraplegia Gene Panel
- 6111KRAS Mutation Screening (Codons 12 & 13)
- 6112Liquid Biopsy 117 Gene Panel
- 6113Liquid Bx. Cell Free BRAF
- 6114Liquid Bx. Cell Free EGFR [T790M,L858R, Exon 19 Deletion]
- 6115Liquid Bx. Cell Free KRAS
- 6116Liquid Bx. Cell Free PAN RAS (KRAS,NRAS)
- 6117Lung Cancer Panel 1 [EGFR, ALK1]
- 6118Lung Cancer Panel 3 [EGFR,ALK1,ROS1,MET]
- 6119Lung Cancer Panel 2 [EGFR,ALK1,ROS1]
- 6120Lung Cancer Panel 4 [EGFR,ALK1,ROS1,MET,PD L1]
- 6121Lung Cancer Panel 5 (EGFR,KRAS,BRAF,ALK1,ROS1)
- 6122Lung Cancer Panel 7 (EGFR,BRAF,ALK1,ROS1,MET)
- 6123Lung Cancer Panel 8 (EGFR,BRAF,ALK,ROS,MET,PDL1)
- 6124Lung Cancer Panel 6 [EGFR by Sequencing,ALK by IHC, ROS1 by FISH]
- 6125Lysosomal Storage Disorder Gene Panel
- 6126MAF/IgH (MM)
- 6127MDM2
- 6128Maturity-Onset Diabetes of the Young (MODY) Gene Panel
- 6130MDS FISH Panel (FISH[del(5q), del(7q), del(20q)])
- 6133Medium Biopsy (1)(Size 1 to 3 cm)
- 6134Medium Biopsy(2) (Size-3 to 5 cm)
- 6136MPZ Full Length Gene Sequence Analysis (Charcot- Maria-Tooth Disease)
- 6138Medium Biopsy(3) (Size 5 to 8 cm)
- 6154Her-2 Neu DNA Detection & Quantification (RNA Detection) Qualitative Test
- 6159h-TERT (RNA Detection) Qualitative Test
- 6165IFN Gamma Quantitative Test
- 6172JC/BK (DNA Detection) (RNA Detection) Qualitative Test
- 6182Malaria (P. Vivax) Quantitative Test
- 6192Measles Virus Viral Load Quantitative Test
- 6240RARA/PML Quantitative Test
- 6257Sibling DNA Test
- 6258Avuncular (Aunt/Uncle) DNA Test
- 6259Grandparent DNA Test
- 6261Whole Exome Sequencing + RAW DATA WES Test
- 6263Paternal Lineage Y-STR Test
- 6265IGHM Gene Agammaglobulinemia Type 1, Autosomal Recessive NGS Genetic Test
- 6266POLG Gene Alper's Syndrome NGS Genetic Test
- 6267Alpha Amino Adipic Aciduria Test
- 6268Alpha Thalassemia Gene Analysis HBA1
- 6269Cell Line Authentication DNA Test
- 6270Liquid Biopsy Lung Cancer Test
- 6273Single Profiling DNA Test
- 6274Liquid Biopsy Colon Cancer Test
- 6280STR Profiling
- 6283Semen FISH
- 6285Comprehensive Tumor Panel 320 Genes
- 6287High Resolution HLA Typing Test
- 6289Comprehensive Tumor Panel 270 Genes+ PDL1
- 6291Legal Paternity DNA Test
- 6292Government Approved Transplant Form 5 DNA Test
- 6293CLN6 Additional Family Members
- 6295Complement-Dependent Cytotoxicity (CDC) Crossmatch
- 6301Vestibular Hypofunction Test
- 6303Microsatellite Instability (MSI) IHC Test
- 6306Limb-Girdle Muscular Dystrophy
- 6308Lynch Syndrome Mismatch Repair (MMR) IHC [MLH1, MLH2, MSH6 & PMS2]
- 6310Limb-girdle muscular dystrophy (LGMD)
- 6314Squash / Zucchini GMO Testing
- 6317Whole Exome+ Mitochondrial Genome Sequencing
- 6330DNA Extraction from Saliva
- 6331DNA Extraction from Milk
- 6344Human Genome Sequencing and Variant Calling-30X
- 6345Rice Genome Sequencing and Variant Calling-30X
- 6346Cattle Genome Sequencing and Variant Calling-10X
- 6347Human Exome Sequencing and Analysis - SureSelect V6
- 6348Rice Genome Sequencing and Variant Calling-10X
- 6349Mitochondrial Genome Sequencing and Analysis
- 6350Human Exome Sequencing and Analysis- Twist Human Core Exome
- 6351Chloroplast Genome Sequencing and Analysis
- 6353Genotyping by Sequencing and Primary Analysis-96 Samples
- 6354ddRAD Sequencing and Primary Analysis-96 Samples
- 6355Human Bisulfite Sequencing and Analysis
- 6358Aptamer Sequencing and Analysis
- 6359MeDIP Sequencing and Analysis
- 6360Hi-C Sequencing and Analysis
- 6362ATAC Sequencing and Analysis
- 6363Cattle Genome Sequencing-10X
- 6365Rice Genome Sequencing-30X
- 6366Rice Genome Sequencing-10X
- 6367Mitochondrial Genome Sequencing
- 6368Human Exome Sequencing- SureSelect V6
- 6370Human Exome Sequencing- Twist Human Core Exome
- 6371ddRAD Library Preparation
- 6372Bisulfite Sequencing Library Preparation
- 6373ChIP-Seq Library Preparation
- 6374DNA Library Preparation-ONT
- 6376PacBio Sequel II Library Preparation
- 6386Human Exome Data Analysis-Variant Calling and Annotation
- 6387Vertebrate Genome Reference Based Data Analysis-Illumina
- 6388Human Genome Reference Based Data Analysis-Illumina
- 6389Diploid Plant Genome Reference Based Data Analysis-Illumina
- 6390Polyploid Plant Genome Reference Based Data Analysis-Illumina
- 6391Vertebrate Genome De Novo Assembly and Annotation-Illumina
- 6392Diploid Plant Genome De Novo Assembly and Annotation-Illumina
- 6393Polyploid Plant Genome De Novo Assembly and Annotation-Illumina
- 6394Mitochondrial Genome Sequencing Data Analysis
- 6396Chloroplast Genome Sequencing Data Analysis
- 6397Genotyping by Sequencing Primary Data Analysis-96 Samples
- 6398Bisulfite Sequencing Data Analysis
- 6399ddRAD Sequencing Primary Data Analysis-96 Samples
- 6401MeDIP Sequencing Data Analysis
- 6403Aptamer Sequencing Data Analysis
- 6404Hi-C Sequencing Data Analysis
- 6414RNA Extraction from Stool
- 6415RNA Extraction from Plasma or Serum
- 6420Eukaryotic Stranded mRNA Sequencing and Reference Based Analysis
- 6421Eukaryotic mRNA Sequencing and Reference Based Analysis
- 6423Eukaryotic Transcriptome Sequencing and Reference Based Analysis-Including lncRNA
- 6424Eukaryotic mRNA Sequencing and Reference Based Analysis-Ultra Low Input
- 6425Eukaryotic mRNA Sequencing and Reference Based Analysis-Low Input
- 6426Eukaryotic Stranded Transcriptome Sequencing and Reference Based Analysis-Including lncRNA
- 6427Eukaryotic mRNA Sequencing and De Novo Analysis
- 6430Eukaryotic Transcriptome Sequencing Reference Based Data Analysis- Including lncRNA
- 6433Eukaryotic SmallRNA Sequencing Data Analysis
- 6436Sequencing Library QC-TapeStation
- 64372x150 Miseq Sequencing-Flow Cell
- 64392x300 Miseq Sequencing-Flow Cell
- 64402x250 Miseq Sequencing-Flow Cell
- 64412x150 Hiseq Sequencing-One Lane
- 64422x150 Hiseq Sequencing- 3 GB
- 64432x150 Hiseq Sequencing- 1 GB
- 64442x150 Hiseq Sequencing- 10 GB
- 64452x150 Hiseq Sequencing- 5 GB
- 64462x150 Hiseq Sequencing- 20 GB
- 6447Oxford Nanopore-Flow Cell
- 6448Heavy Metals Mini Profile Test
- 6450PacBio Sequel- 30 GB
- 6451PacBio Sequel- 1GB
- 6452Oxford Nanopore- 1GB
- 6454Heavy Metals Maxi Profile
- 6458Food Intolerance Allergy Test
Articles Reviewed by Dr Pasupathy Arumugam
- Parosteal Osteosarcoma Symptoms: Early Warning Signs and DiagnosisGenomic & Hereditary Oncology • Sep 09, 2026
- Vaginal Squamous Cell Carcinoma: Symptoms, Diagnosis, and PreventionGenomic & Hereditary Oncology • Sep 09, 2026
- Oral Cancer Squamous Cell Carcinoma: Symptoms, Diagnosis, and PreventionGenomic & Hereditary Oncology • Sep 09, 2026
- Liquid Biopsy Cancer Test in India: Cost, Accuracy & Early Detection GuideGenomic & Hereditary Oncology • Sep 10, 2026