0172-5017001 / +91 628 421 4977 support@altuslab.in 7:30 AM - 9:30 PM Daily
Home Departments Genetic Tests
NABL Certified

Genetic Tests

From thalassaemia carrier screening and prenatal chromosomal analysis to BRCA mutation testing and pharmacogenomics, Altus Lab provides the molecular genetic diagnostics that inform lifelong health decisions.

Call Now

Tests Available at Altus Lab

1

Karyotyping (Peripheral Blood, Products of Conception, Amniotic Fluid)

Numerical and structural chromosomal abnormalities — Down syndrome, Turner, Klinefelter, balanced translocations

2

FISH (Fluorescence In Situ Hybridisation)

Rapid targeted chromosomal anomaly detection — trisomies 13/18/21, microdeletions (22q11, 15q, etc.)

3

Chromosomal Microarray (CMA/SNP-Array)

High-resolution genome-wide copy number variation — detects submicroscopic deletions/duplications missed by karyotype

4

Haemoglobin HPLC (Beta-Thalassaemia & Sickle Cell Screening)

Identifies all thalassaemia traits, HbS, HbC, HbE and other haemoglobinopathies

5

Beta-Thalassaemia Mutation Panel (Gap-PCR / Sequencing)

Molecular confirmation of thalassaemia mutations — essential for genetic counselling and prenatal diagnosis

6

Alpha-Thalassaemia Deletion Analysis (Gap-PCR)

Detects alpha-globin gene deletions — important in hydrops fetalis risk assessment

7

Non-Invasive Prenatal Testing (NIPT/NIFTY)

Cell-free DNA from maternal blood — screens for trisomies 21, 18, 13, sex chromosome aneuploidies with >99% sensitivity

8

Prenatal Chromosomal Analysis (Amniocyte/CVS Karyotype)

Invasive prenatal diagnosis for high-risk pregnancies

9

BRCA1 & BRCA2 Mutation Analysis (NGS Panel)

Hereditary breast and ovarian cancer risk — guides prophylactic surgery and targeted therapy decisions

10

Lynch Syndrome Panel (MLH1, MSH2, MSH6, PMS2)

Hereditary colorectal cancer and endometrial cancer predisposition

11

Fragile X Syndrome (FMR1 CGG Repeat Expansion)

Most common inherited cause of intellectual disability and autism spectrum disorder

12

Spinal Muscular Atrophy (SMA — SMN1/SMN2 Copy Number)

SMA carrier screening and diagnosis — gene therapy eligibility (Zolgensma/Spinraza)

13

Pharmacogenomics Panel (CYP2D6, CYP2C19, CYP2C9, SLCO1B1, DPYD)

Predicts drug metabolism phenotype — guides safe dosing of antidepressants, clopidogrel, warfarin, statins, chemotherapy

14

MTHFR Mutation Analysis (C677T & A1298C)

Elevated homocysteine, recurrent miscarriage and neural tube defect risk

15

JAK2 V617F Mutation (BCR-ABL, MPL, CALR)

Myeloproliferative neoplasm (polycythaemia vera, ET, MF) molecular diagnosis

16

BCR-ABL1 Quantitative PCR (CML Monitoring)

Chronic myeloid leukaemia — treatment response and remission monitoring

17

Y Chromosome Microdeletion (AZF a/b/c)

Male infertility — azoospermia and severe oligospermia investigation

Why Choose Altus Lab

NABL Accredited Quality

Every genetic tests test is processed under a quality management system certified by India's National Accreditation Board — the same standard as international reference laboratories.

Expert Pathologist Review

Dr. Alok Gupta (MD Pathology, CMC Ludhiana; PGI Senior Residency, Apollo & Vimta Labs experience) personally reviews complex and critical results before dispatch.

Free Home Collection

Trained phlebotomists visit your home across Chandigarh, Mohali and Panchkula. Book a slot and we take care of everything — sample to digital report.

Fast Digital Reports

Most genetic tests results are available within 4–6 hours. Emergency and critical samples are processed immediately with direct physician notification.

Frequently Asked Questions

Karyotyping visualises all 46 chromosomes under a microscope and detects large-scale abnormalities (>5–10 Mb). Chromosomal Microarray (CMA) analyses copy number variations at a resolution 100× higher — detecting tiny deletions and duplications (sub-megabase) that karyotyping misses entirely. CMA is increasingly preferred for developmental delay, autism, and unexplained pregnancy loss.
Yes, strongly. Beta-thalassaemia has a carrier frequency of approximately 3–4% in Punjab and surrounding states. If both partners are carriers (beta-thalassaemia trait), there is a 25% chance with each pregnancy of having a child with severe thalassaemia major requiring lifelong transfusions. Pre-marital HPLC screening followed by molecular confirmation enables informed family planning decisions.
Non-Invasive Prenatal Testing (NIPT) analyses cell-free foetal DNA in maternal blood, with detection rates exceeding 99% for Down syndrome (trisomy 21) and false positive rates below 0.1%. This is significantly superior to the triple marker test (sensitivity ~69%) and quadruple screen. NIPT is recommended from 10 weeks gestation onwards for all pregnant women, particularly those ≥35 years or with a prior chromosomal pregnancy.
Your genes encode the enzymes that metabolise most medications. Variations in genes like CYP2D6 and CYP2C19 can make you a poor metaboliser (increased drug toxicity) or ultra-rapid metaboliser (reduced drug effect) for common medications including antidepressants, antiplatelets (clopidogrel), proton pump inhibitors, and certain chemotherapy agents. A pharmacogenomics panel can guide your doctor to prescribe the right drug at the right dose from the outset.
Insurance coverage for genetic testing varies by policy. BRCA testing is covered by some policies when there is a strong family history of breast/ovarian cancer. Prenatal testing (NIPT, karyotyping) is covered by some group health policies. We recommend checking your policy documents or contacting your insurer directly. Our team can provide detailed bills and clinical justification letters to support insurance claims.

Book Your Genetic Tests Test in Chandigarh Today

100% Accurate results · Free home collection · PGI-accepted reports · Open 7 days

📞 Call: 0172-5017001
Serving Since 2013
Reports in 4–6 Hours
Free Home Collection
PGI & GMCH-Accepted Reports
330+ Trusted Physicians
WhatsApp Us Call Now · 4hr Reports