Routine & Wellness Checks
DNA Labs India | Diagnostic Tests
Routine & Wellness Checks
Clinical Overview
Sub-category mapping under Genetics & Genomics
| Reviewed by: Dr. Rajesh Kumar, MD Pathology | ISO 9001:2015 Certified Laboratory
This content is for educational purposes only. Always consult a qualified healthcare provider for medical advice.
Tests
Alpha-1-Antitrypsin Quantitation (AAT) Test
To diagnose Alpha-1-Antitrypsin deficiency by measuring AAT levels in the blood, aiding in the asses...
Analyzer 26 SMA 26 Test Panel
The purpose of the Analyzer 26 SMA 26 Test Panel is to diagnose spinal muscular atrophy by assessing...
CEBPA Mutation Detection Test
The purpose of the CEBPA Mutation Detection Test is to identify mutations in the CEBPA gene, which c...
Chromosomal Microarray (CMA) 750K High Resolution Test
The purpose of the Chromosomal Microarray (CMA) 750K High Resolution Test is to identify genetic cau...
Cystic Fibrosis Newborn Screen Test
The Cystic Fibrosis Newborn Screen Test is performed to detect elevated levels of Immunoreactive Try...
FISH - Prenatal Comprehensive Screening Panel 1 Test
To detect aneuploidy for Trisomy 13, 18, 21, and sex chromosomes, as well as microdeletions for DiGe...
Genetic Counselling and Genetic Test
The purpose of genetic counselling is to provide personalized guidance on genetic risks, interpret t...
Whole Genome Test
The purpose of the Whole Genome Test is to identify genetic variations that may indicate predisposit...
Hemoglobinopathy Newborn Screen Test
To identify hemoglobinopathies in newborns early for prompt treatment and management, preventing ser...
IMD Panel Quantitative Blood Test
The purpose of the IMD Panel Quantitative Blood Test is to detect and quantify biomarkers associated...
Microarray Gene Chip Scanning Test
For scanning Affymetrix Gene chips to detect genetic abnormalities and mutations for diagnostic and...
Newborn Screening Panel: NBS Quad Test
The NBS Quad Test is designed to screen newborns for four critical conditions: Phenylketonuria (PKU)...
Newborn Screening Panel 7 Test
The purpose of the Newborn Screening Panel 7 Test is to identify seven potentially serious genetic a...
NGS Gen Whole Exome Sequencing Trio Test
The purpose of the NGS Whole Exome Sequencing Trio Test is to perform whole exome sequencing on the...
Newborns Genetic Test Panel NGS Genetic Test
The purpose of the Newborn Genetic Test Panel is to identify genetic disorders early in life, enabli...
SKI Gene Shprintzen-Goldberg syndrome NGS Genetic Test
The purpose of the SKI Gene NGS Genetic Test is to identify mutations in the SKI gene associated wit...
Frozen-2
To diagnose genetic disorders by identifying mutations in DNA.
Chromosomal Microarray 315K (AF/CVS/CB/POC/PB)
The purpose of the Chromosomal Microarray 315K test is to detect genetic abnormalities, such as dele...
Microarray 180K (AF/CVS/CB/POC/PB)
The purpose of the Microarray 180K test is to identify chromosomal abnormalities and genetic variati...
Microarray 750K+ Single Karyotyping (AF/CVS/CB/POC/PB)
The purpose of Microarray 750K+ Single Karyotyping is to identify chromosomal abnormalities that may...
NIPT Microdeletion Test
To screen for fetal microdeletion syndromes non-invasively, aiding in early risk assessment and guid...
Peripheral Blood for Karyotyping (Single)
The purpose of Peripheral Blood for Karyotyping is to analyze chromosomes for numerical or structura...
Sickle Cell Mutation Screening [Prenatal]
The purpose of Sickle Cell Mutation Screening [Prenatal] is to identify the presence of sickle cell...
Spinal Muscular Atrophy Screening [Prenatal]
The purpose of Spinal Muscular Atrophy prenatal screening is to detect SMN1 gene mutations in the fe...
Targeted Mutation Analysis (1 Mutation)
The purpose of Targeted Mutation Analysis is to confirm the presence of a specific genetic mutation...
Targeted Mutation Analysis (2 Mutations)
The purpose of targeted mutation analysis is to detect specific genetic mutations that are associate...
William's Syndrome (Karyotyping+FISH)
To diagnose Williams Syndrome by detecting deletion on chromosome 7q11.23 through karyotyping and FI...
Targeted Sequencing- Below 50 Kb
The purpose of targeted sequencing below 50 Kb is to diagnose genetic disorders by sequencing specif...
Comprehensive Hereditary Cancer Panel - 157 Genes Test
The purpose of this test is to identify genetic variants that increase the risk of hereditary cancer...
CCBE1 Gene Hennekam lymphangiectasia-lymphedema syndrome type 1 NGS Genetic Test
To diagnose Hennekam lymphangiectasia-lymphedema syndrome type 1 by detecting mutations in the CCBE1...
MTRR Gene Spina bifida folate sensitive NGS Genetic Test
The purpose of this test is to identify mutations in the MTRR gene that may increase susceptibility...
Beta Thalassemia Screening [Prenatal]
The purpose of this prenatal screening is to identify whether the fetus has inherited beta thalassem...
Prenatal Delta Beta-Thalassaemia Mutation Screening
The purpose of prenatal delta beta-thalassaemia mutation screening is to determine whether a develop...
HbE (Hemoglobin E) Mutation Screening [Prenatal]
The purpose of HbE prenatal screening is to determine whether the fetus has inherited the HbE mutati...
The Non-Invasive Prenatal (NIPT) Twins Test
The primary purpose of the NIPT Twins Test is to screen for the most common chromosomal aneuploidies...
Dog DNA Test
The primary purpose of the Dog DNA Test is to establish genetic lineage, identify breed composition,...
Horse DNA Test
The primary purpose of the Horse DNA Test is to detect genetic mutations associated with hereditary...
Buffalo DNA Test
The primary purpose of the Buffalo DNA Test is to support livestock health and breeding management....
Genetic Test Counselling
The purpose of genetic test counselling is to provide individuals and families with a clear understa...
DNA Extraction from Solid Tissue - Animal
The purpose of DNA extraction from solid tissue in animals is to isolate high-quality genomic DNA fo...
Cattle Genome Sequencing-30X
The primary purpose of cattle genome sequencing is to provide a complete genetic profile of an indiv...