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NIPT (Non Invasive Prenatal Testing)

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Rs. 15,000.00
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NIPT (Non Invasive Prenatal Testing) - Mapmygenome
NIPT (Non Invasive Prenatal Testing) - Mapmygenome
BENEFITS +

• Non-Invasive & Safe: No risk to mother or baby — uses cell-free DNA from maternal blood.
• Early Detection: Screens for chromosomal abnormalities as early as 10 weeks into pregnancy.
• High Accuracy: Advanced NGS technology delivers high sensitivity and low false-positive rates.
• Comprehensive Screening: Detects trisomies 13, 18, 21 and sex chromosomal anomalies.
• Quick Results: Report available within 2 weeks of sample collection.

WHAT'S INCLUDED +

🧬 NIPT Screening Panels

Autosomal Trisomies:
Trisomy 21 (Down Syndrome), Trisomy 18 (Edwards Syndrome), Trisomy 13 (Patau Syndrome)

Sex Chromosomal Aneuploidies:
Monosomy X (Turner Syndrome), XXY (Klinefelter Syndrome), XYY, XXX

Fetal Sex Determination:
Optional fetal sex assessment from cell-free DNA

SAMPLE TYPE +

  • 10 ml maternal blood in streck tube

TESTING TECHNIQUE +

Non-Invasive Prenatal Testing (NIPT) using Next Generation Sequencing (NGS) to analyze cell-free fetal DNA (cffDNA) circulating in maternal blood. Detects copy number variants and chromosomal aneuploidies including trisomies 13 (Patau syndrome), 18 (Edwards syndrome), 21 (Down syndrome), and sex chromosomal anomalies. Requires 10 ml maternal blood in streck tube.

• Non-Invasive & Safe: No risk to mother or baby — uses cell-free DNA from maternal blood.
• Early Detection: Screens for chromosomal abnormalities as early as 10 weeks into pregnancy.
• High Accuracy: Advanced NGS technology delivers high sensitivity and low false-positive rates.
• Comprehensive Screening: Detects trisomies 13, 18, 21 and sex chromosomal anomalies.
• Quick Results: Report available within 2 weeks of sample collection.

Features

  • Personalized and Actionable

  • Pan India Shipping

  • Digital Reports

  • Secure Personal Data

FAQs

Who can benefit from this test ?

NIPT is generally recommended to all pregnant woman.

If any soft marker tests (double, triple & quadruple marker) suggest for chromosomal abnormalities.

If ultrasound High NT or absent nasal bone suggests for chromosomal abnormalities.

History of a prior pregnancy with a trisomy.

How do we analyze?

Uses Next Generation Sequencing to identify copy number variants

How long does it take to get the report?

2 Weeks