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NIPT Test in Bangalore – Understand What It Screens For Before You Decide

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Benefits of NIPT Test

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Early Detection:

NIPT can detect chromosomal abnormalities and genetic conditions as early as 10 weeks into pregnancy, providing you with crucial information sooner.
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Accuracy

NIPT has a high accuracy rate in identifying conditions like Down syndrome (Trisomy 21), Edwards syndrome (Trisomy 18), and Patau syndrome (Trisomy 13), reducing the likelihood of false positive or false negative results.
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Peace of Mind

A negative NIPT result provides reassurance and may reduce the need for invasive tests like amniocentesis, which carry higher risks.

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79/7, Bellandur Service Road, Near Xochi Restaurant, Bengaluru 560103 hello@hercare.in +91 8148340982

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Know more about NIPT Test

Thinking about NIPT only because someone told you to? This test screens for common chromosomal conditions but it is not diagnostic. Here's how to decide if it's right for your pregnancy. Non-Invasive Prenatal Testing (NIPT) is a blood test that screens for chromosomal conditions like Down syndrome (Trisomy 21), Edwards syndrome (Trisomy 18), and Patau syndrome (Trisomy 13). It can be done from 10 weeks of pregnancy onwards. What NIPT CAN screen for: • Down syndrome (Trisomy 21) - >99% detection rate • Edwards syndrome (Trisomy 18) • Patau syndrome (Trisomy 13) • Sex chromosome conditions (optional) • Microdeletions (with advanced panels) What NIPT CANNOT do: • Diagnose conditions with 100% certainty (it's a screening test) • Detect all genetic conditions • Replace diagnostic tests like amniocentesis if positive NIPT Test in Bangalore - Pricing: • Basic NIPT (5 parameters): ₹12,000 • Panorama NIPT (all 23 chromosomes): ₹14,000 • NIPT with Microdeletions: ₹24,500 NIPT Test Near Bellandur, Koramangala, HSR Layout & Marathahalli Her Care offers NIPT testing through NABL-accredited partners (MedGenome, Anand Neuberg). We provide FREE home sample collection across Bangalore. Located on Bellandur Service Road, easily accessible from Koramangala, HSR Layout, Marathahalli, and Sarjapur Road.

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Frequently Asked Questions

What is NIPT? close
NIPT (Non-Invasive Prenatal Testing) is an advanced screening test that analyzes fetal DNA in the mother's blood to assess the risk of certain chromosomal conditions, such as Down syndrome, trisomy 18, and trisomy 13.
What is NIPT Test Cost? close
Basic NIPT Test Cost is Rs.12,000. Our Medgenome package for NIPT Testing cost is 14,000 including FREE home collection. The NIPT Test price with microdeletions is Rs.24,500 including FREE home collection.
When is NIPT typically performed? close
NIPT is usually done between the 9th and 10th weeks of pregnancy, though it can often be performed as early as the 10th week.
How is NIPT different from other prenatal tests? close
Unlike invasive tests like amniocentesis, NIPT is non-invasive and carries no risk of miscarriage. It provides valuable information about chromosomal conditions with a simple blood draw.
What conditions can NIPT screen for? close
NIPT primarily screens for common chromosomal conditions like Down syndrome (trisomy 21), Edwards syndrome (trisomy 18), and Patau syndrome (trisomy 13). Some NIPT tests also screen for specific chromosome abnormalities.
How accurate is NIPT? close
NIPT is known for its high accuracy rate, generally having a sensitivity of over 99% for detecting Down syndrome and other trisomies.
Does NIPT reveal the gender of the baby? close
No, due to PCPNDT Act of 1994, the gender of the baby can't be revealed in India.
Is NIPT suitable for all pregnancies? close
NIPT is often recommended for pregnancies at increased risk of chromosomal conditions, including advanced maternal age or a history of genetic disorders. It can also be used for low-risk pregnancies, though the decision is often based on individual circumstances.
Does insurance cover NIPT? close
Many insurance plans cover NIPT if certain criteria are met, such as being considered high-risk by medical guidelines. It's important to check with your insurance provider to understand coverage.
Are there any limitations to NIPT? close
While NIPT is highly accurate, it's still considered a screening test, and false positive/negative results can occur. Positive NIPT results should be followed up with confirmatory testing like amniocentesis.
Can NIPT detect all genetic conditions? close
NIPT primarily focuses on specific chromosomal conditions. It may not detect rare genetic conditions or single gene mutations. Genetic counseling can help you understand what NIPT can and cannot screen for.
Till what weeks can NIPT be done? close
NIPT can typically be done from the 10th week of pregnancy onwards. Most women do it between 10-14 weeks. It can be performed later in pregnancy too, though earlier testing gives more time for planning.
Do you offer home sample collection for NIPT in Bangalore? close
Yes, we offer FREE home sample collection for NIPT across Bangalore. Our phlebotomist will visit your home at a convenient time to collect the blood sample.
How long do NIPT results take? close
NIPT results typically take 7-10 working days. The sample is processed at NABL-accredited labs (MedGenome, Anand Neuberg) to ensure accuracy.
What is the difference between Basic NIPT and NIPT with Microdeletions? close
Basic NIPT (₹12,000) screens for 5 parameters - Trisomy 13, 18, 21, and sex chromosomes (X and Y). NIPT with Microdeletions (₹24,500) screens all 23 chromosomes plus microdeletion syndromes like DiGeorge syndrome, providing more comprehensive screening.
Is NIPT better than NT scan and Double Marker test? close
NIPT has a higher detection rate (>99% for Down syndrome) compared to NT scan + Double Marker combined screening (~85-90%). However, NIPT is more expensive. Many doctors recommend NT scan first, and NIPT if the combined screening shows intermediate or high risk.
Where can I get NIPT test in Bangalore? close
Her Care offers NIPT testing at our Bellandur clinic (near Xochi Restaurant) with free home collection across Bangalore. We serve Bellandur, Koramangala, HSR Layout, Marathahalli, Sarjapur Road, and surrounding areas.
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