If you are looking for a genetic testing panel in Chandigarh, Altus Lab offers specialist molecular and chromosomal diagnostics with free home collection across Chandigarh, Mohali, and Panchkula. Genetic testing analyses an individual’s DNA to identify inherited mutations, chromosomal abnormalities, and hereditary disease risks. Because genetic results have lifelong implications — for the patient and for their family — testing at a specialist laboratory with expert oversight is essential.
Our lab is founded and led by an Ex-PGIMER Chandigarh doctor with over 13 years of specialist diagnostic experience. Furthermore, because we operate our own in-house molecular laboratory, we process samples with direct specialist oversight — which consequently means higher accuracy and faster results. Doctors at PGIMER, GMCH-32, GMCH-16, Fortis Mohali, and Max Hospital accept our genetic reports for clinical decision-making.
What Is Genetic Testing?
Genetic testing examines your DNA — the chemical database that carries instructions for your body’s functions. Tests may look at a single gene, a panel of genes, all chromosomes (karyotype), or specific DNA sequences associated with known hereditary diseases. The results can confirm a diagnosis, identify carrier status, assess cancer risk, guide medication dosing (pharmacogenomics), or inform reproductive decisions before or during pregnancy.
Genetic Tests Available at Altus Lab Chandigarh
| # | Test | Purpose | Who Needs It |
|---|---|---|---|
| 1 | Karyotyping (Chromosome Analysis) | Detects chromosomal abnormalities — extra, missing, or rearranged chromosomes | Recurrent miscarriage, infertility, developmental delay, Down syndrome screening |
| 2 | BRCA1 / BRCA2 Gene Testing | Identifies hereditary breast and ovarian cancer mutations | Women with strong family history of breast or ovarian cancer before age 50 |
| 3 | Thalassaemia Gene Mutation Panel | Identifies alpha and beta thalassaemia mutations at the DNA level | Couples planning pregnancy where one or both partners carry thalassaemia trait |
| 4 | MTHFR Gene Mutation | Identifies C677T and A1298C variants affecting folate metabolism | Recurrent miscarriage, hyperhomocysteinaemia, neural tube defect history |
| 5 | Fragile X Syndrome Testing (FMR1) | Detects CGG repeat expansion in FMR1 gene | Intellectual disability of unknown cause in males; premature ovarian insufficiency in women |
| 6 | Cystic Fibrosis Mutation Panel | Detects CFTR gene mutations including deltaF508 | Recurrent respiratory infections, infertility in males, newborn screening follow-up |
| 7 | FISH (Fluorescence In Situ Hybridisation) | Rapid detection of specific chromosomal deletions and duplications | Haematological malignancies, specific microdeletion syndromes |
| 8 | Pharmacogenomics Panel | Identifies gene variants affecting drug metabolism (CYP2C19, CYP2D6, etc.) | Patients on clopidogrel, warfarin, antidepressants, or oncology drugs with variable responses |
| 9 | NIPT (Non-Invasive Prenatal Testing) | Cell-free fetal DNA screening for chromosomal aneuploidies | Pregnant women from 10 weeks gestation for Down, Edwards, and Patau syndrome screening |
Who Should Get Genetic Testing in Chandigarh?
- Couples planning pregnancy with a family history of thalassaemia, sickle cell disease, or other inherited conditions
- Women with recurrent miscarriage (two or more consecutive losses) — for chromosomal and MTHFR testing
- Pregnant women over 35 or with abnormal first-trimester screening results — for NIPT or karyotyping
- Women with a strong family history of breast or ovarian cancer — for BRCA1/BRCA2 testing
- Children with unexplained developmental delay, intellectual disability, or multiple congenital anomalies
- Patients with a personal or family history of hereditary colorectal cancer syndromes (Lynch Syndrome, FAP)
- Cancer patients before targeted therapy — as pharmacogenomics guides drug selection and dosing
- Individuals referred by geneticists or specialists at PGIMER Chandigarh’s genetic counselling department
Genetic Counselling — What Happens After Your Test?
A genetic test result can have profound implications for the patient and their entire family. Altus Lab therefore strongly recommends that all patients undergoing genetic testing discuss their results with a qualified genetic counsellor or specialist. The genetics department at PGIMER Chandigarh provides comprehensive genetic counselling services and is the primary referral centre for complex hereditary conditions in North India. We will ensure your report is formatted and annotated for seamless review at PGIMER or any other specialist centre of your choice.
Why Choose Altus Lab for Genetic Testing in Chandigarh?
- Founded by an Ex-PGIMER Chandigarh Doctor — molecular diagnostics with specialist oversight
- Own In-House Molecular Lab — PCR-based and FISH-based genetic tests processed on-site
- Reports Accepted at PGIMER Genetics Department — seamless integration with specialist care
- Free Home Collection — across Chandigarh, Mohali, Panchkula, Zirakpur, and Kharar
- Digital Reports via WhatsApp and Email — with specialist annotations for your genetic counsellor
- Strict Confidentiality — genetic results are handled with the highest level of patient privacy
Frequently Asked Questions — Genetic Testing in Chandigarh
Is genetic testing confidential at Altus Lab?
Yes. All genetic test results at Altus Lab are treated with the strictest confidentiality. Results are shared only with the patient and their designated physician. We do not share genetic data with third parties under any circumstances.
Can I get BRCA testing done at home in Chandigarh?
Yes. Altus Lab provides free home blood sample collection for BRCA1/BRCA2 testing across Chandigarh, Mohali, and Panchkula. The sample is then processed in our molecular laboratory. Results are typically available within 10–14 working days due to the complexity of the sequencing process.
What is NIPT and when should I get it done during pregnancy?
NIPT (Non-Invasive Prenatal Testing) is a blood test that analyses cell-free fetal DNA circulating in the mother’s blood. It can screen for chromosomal conditions such as Down syndrome (Trisomy 21), Edwards syndrome (Trisomy 18), and Patau syndrome (Trisomy 13) from as early as 10 weeks of pregnancy. It is the most accurate non-invasive prenatal screening test currently available.
We are both thalassaemia carriers. What genetic tests do we need before pregnancy?
If both partners carry thalassaemia trait, there is a 25% chance of each pregnancy resulting in thalassaemia major. Altus Lab can perform detailed thalassaemia mutation panel testing to identify the specific mutations you carry. This information is then used for prenatal diagnosis (CVS or amniocentesis) if you conceive. Please consult the haematology and genetics department at PGIMER Chandigarh for comprehensive pre-pregnancy counselling.
Book Your Genetic Testing Panel in Chandigarh Today
Genetic knowledge is powerful — it enables prevention, early treatment, and informed reproductive decisions. Book your genetic testing panel at Altus Lab Chandigarh and receive accurate, specialist-reviewed results that your doctor at PGIMER, Fortis Mohali, or GMCH-32 can rely on.
Call Now: 0172-5017001 / 0172-5017002
Available: 7:30 AM – 9:30 PM Daily
Free Home Collection: Chandigarh | Mohali | Panchkula | Zirakpur
Founded by Ex-PGIMER Doctor | Own In-House Molecular Lab | Strict Confidentiality