Chromosomes 13 & 21 Test
Also known as: FISH for Chromosomes 13 and 21, Prenatal Chromosomal Analysis
Chromosomes 13 & 21 Test test available at DNA Labs India for ₹6,000. Uses FISH on Amniotic fluid / Chorionic villi / Cord blood samples. Results in 3-4 days. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr Pasupathy Arumugam
Consultant Pathologist · Reg: 21521
Last reviewed: September 7, 2026
Overview
The purpose of Chromosomes 13 & 21 testing is to identify numerical or structural abnormalities in chromosomes 13 and 21, which can lead to genetic disorders such as Down syndrome (trisomy 21) and Patau syndrome (trisomy 13). This test aids in prenatal diagnosis, risk assessment, and genetic counseling, enabling early medical intervention and informed decision-making for patients and healthcare providers.
- Test Code
- 2965
- Price
- ₹6,000
- Sample Type
- Amniotic fluid / Chorionic villi / Cord blood
- Result Time
- 3-4 days
- Fasting Required
- No
- Method
- FISH
Sample Collection
A doctor's prescription may be required, except for pregnancy cases or individuals planning to travel abroad. Ensure proper documentation is provided.
Laboratory Analysis
Sample collection is performed by a trained phlebotomist or healthcare professional using sterile techniques to avoid contamination.
Report Delivery
Samples are transported to the laboratory under appropriate conditions (ambient or cool pack) for analysis.
Timeline: 3-4 days
Patient Instructions
About This Test
Who Should Get This Test
The purpose of Chromosomes 13 & 21 testing is to identify numerical or structural abnormalities in chromosomes 13 and 21, which can lead to genetic disorders such as Down syndrome (trisomy 21) and Patau syndrome (trisomy 13). This test aids in prenatal diagnosis, risk assessment, and genetic counseling, enabling early medical intervention and informed decision-making for patients and healthcare providers.
How to Prepare
- Use sterile containers for sample collection
- For amniotic fluid, chorionic villi, or cord blood, follow aseptic procedures
- Label samples correctly with patient details
Doctor's Notes
Reviewed by Dr Pasupathy Arumugam — MBBS, MD (Pathology) · Reg. No. 21521
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
- Contaminated samples
- Improperly labeled specimens
- Insufficient sample volume
Understanding Your Results
Normal
Two copies of chromosomes 13 and 21 detected, indicating no abnormalities.
Abnormal
Additional or missing copies detected, suggesting chromosomal disorders; further genetic counseling and testing recommended.
Consult a doctor if you experience symptoms of chromosomal abnormalities, have a family history of genetic disorders, are pregnant with risk factors, or receive abnormal test results for appropriate management and counseling.
Limitations
- ⚠Test may not detect all chromosomal abnormalities
- ⚠Results require confirmation with additional tests in some cases
Risks & Considerations
- ●For invasive sample collection (e.g., amniocentesis), risks include infection, miscarriage, or discomfort
- ●Minimal risks for blood sample collection
Frequently Asked Questions
What is Chromosomes 13 & 21 testing?
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₹6,000Reference Laboratory Services
We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.
Your Data Privacy
Your medical data is protected under Indian law.
✓ Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.
✓ DPDP Act Compliant: Under the Digital Personal Data Protection Act 2023, you can request deletion of your records at any time by contacting support.
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