Skip to main content
DNA Labs India

Newborns Genetic Test Panel NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

Newborns Genetic Test Panel NGS Genetic Test

Short Name: Newborn Genetic Panel NGS

Also known as: Newborn Genetic Screening Panel, NGS Newborn Test

Newborns Genetic Test Panel NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS Technology on Blood or Extracted DNA or One drop Blood on FTA Card samples. Results in 3 to 4 Weeks. Free home collection in 300+ cities across India.

Diagnostic ScreeningNeonatal (0-28 days)🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of the Newborn Genetic Test Panel is to identify genetic disorders early in life, enabling prompt medical management, reducing complications, and providing families with essential information for healthcare planning and genetic counselling.

Test Code
1849
Price
₹20,000
Sample Type
Blood or Extracted DNA or One drop Blood on FTA Card
Result Time
3 to 4 Weeks
Fasting Required
No
Method
NGS Technology
Step 1

Sample Collection

Ensure the newborn is stable for blood draw. Inform the healthcare provider of any medical history.

Method: Venipuncture or FTA Card Collection

Step 2

Laboratory Analysis

Blood sample will be collected via venipuncture or using an FTA card for a drop of blood.

Step 3

Report Delivery

Apply pressure to the puncture site to prevent bleeding. Monitor for any signs of discomfort.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Genetic counselling session recommended to understand the test and draw a family pedigree chart.
2
During the Test:The test involves NGS technology to sequence DNA and identify mutations.
3
After the Test:Results will be reviewed by a geneticist, and a report will be provided with recommendations.

About This Test

Who Should Get This Test

The purpose of the Newborn Genetic Test Panel is to identify genetic disorders early in life, enabling prompt medical management, reducing complications, and providing families with essential information for healthcare planning and genetic counselling.

How to Prepare

  • Use sterile equipment for sample collection
  • Label the sample correctly with patient details
  • Store at ambient room temperature if using FTA card

Doctor's Notes

Reviewed by — MBBS, MD (Pathology) · Reg. No. 21521

"Early genetic screening in newborns can be crucial for timely intervention, improving health outcomes and guiding family planning."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Collection MethodVenipuncture or FTA Card Collection

Sample Stability

Blood sample stable for 24 hours at room temperature
Extracted DNA stable for longer periods if stored properly
Sample Rejection Criteria:
  • Hemolyzed or contaminated samples
  • Incorrect labeling or insufficient sample volume
  • Sample not stored under recommended conditions

Understanding Your Results

Results are interpreted based on the detection of specific genetic mutations. A positive result indicates the presence of a disorder, while a negative result suggests no detected variants in the screened genes.
Positive result: Consult a geneticist for confirmation and management options
Negative result: Continue regular pediatric care, but note that not all disorders are covered
Variant of uncertain significance: May require further testing or genetic counselling
⚠️ When to Consult a Doctor:

Consult a doctor immediately if the test indicates a genetic disorder, or if the newborn shows symptoms such as developmental delays, seizures, or feeding difficulties.

Limitations

  • May not detect all possible genetic variants
  • False positives or negatives possible in rare cases
  • Does not cover all genetic disorders, only those in the panel

Risks & Considerations

  • Minimal risk from blood draw, such as bruising or infection
  • Psychological impact from test results, mitigated by genetic counselling

Interfering Factors

  • Poor sample quality or insufficient DNA
  • Contamination during sample collection
  • Recent blood transfusion affecting DNA analysis

Compare With Similar Tests

TestNewborns Genetic Test Panel NGS Genetic TestCystic Fibrosis Carrier ScreeningSickle Cell Anemia TestWhole Exome SequencingKaryotyping
ComparisonNewborns Genetic Test Panel NGS Genetic TestFocuses on a single disorder; broader panel covers multiple disordersSpecific to hemoglobin disorders; NGS panel includes various genetic conditionsMore comprehensive but costlier; this panel is targeted for newbornsDetects chromosomal abnormalities; NGS panel detects gene mutations

Frequently Asked Questions

What is the Newborn Genetic Test Panel?
It is a diagnostic test using NGS technology to screen newborns for multiple genetic disorders or abnormalities.
Why should I get this test for my newborn?
Early detection of genetic disorders allows for timely intervention, better management, and improved health outcomes.
What is the cost of the test?
The test costs INR 20,000 at DNA Labs India, with free home sample collection available.
What samples are required for the test?
A blood sample, extracted DNA, or one drop of blood on an FTA card can be used.
Is fasting required before the test?
No, fasting is not required for this genetic test.
How long does it take to get the results?
Results are typically available within 3 to 4 weeks after sample collection.
What disorders does the test screen for?
The test includes a range of genetic disorders such as metabolic disorders, heart defects, and developmental conditions.
Is the test accurate?
NGS technology is highly accurate, but like any test, there is a small chance of false positives or negatives.
Do I need genetic counselling?
Yes, a genetic counselling session is recommended before the test to understand implications and draw a family pedigree chart.
Is home sample collection available?
Yes, DNA Labs India offers free home sample collection in numerous cities across India.
What if the test results are positive?
Consult a geneticist or specialist for confirmation, further testing, and management options.
Are there any risks associated with the test?
The test has minimal risks, primarily related to blood draw, such as bruising or infection.
Worried about the process? Our certified phlebotomists collect thousands of samples every month across India. The process takes under 5 minutes and is virtually painless. Questions? Message us on WhatsApp — we're here 7 days a week.

Related Tests

For Hospitals & Clinics

Reference 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.

LIMS Integration

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.

Book Your Test

Enter your details and we'll connect you within 15 minutes.

🧬

Quick Connect

Enter your mobile number and we’ll connect you with the team.

+91

✅ Connecting you now...

🔒 Your number is used to respond to this request.