Pregnancy - NIPT
NIPT Philippines (Non-Invasive Prenatal Test)
A safer way to learn more about your baby's health during pregnancy
Pregnancy comes with many questions, and every parent wants reassurance that their baby is developing well. Lablog's Non-Invasive Prenatal Test (NIPT) is an advanced prenatal genetic screening test that analyzes fragments of your baby's DNA through a simple blood sample from the mother. There is no risk to the baby, no risk to the pregnancy, and no invasive procedures required. Powered by NIFTY by BGI Genomics, one of the world's leading genomics organizations, our NIPT provides highly accurate screening for common chromosomal conditions early in pregnancy.
As Early As
10 Weeks
Simple
Maternal Blood Draw
99%+
Trisomy Accuracy
No Risk
To Mother Or Baby
ISO-Certified
Partner Laboratory
Powered By
NIFTY by BGI
Collection
Centers Nationwide
Mobile
Home Service
Strictly
Confidential
Results In
10-15 Working Days
Important: NIPT is a screening test and not a diagnostic test. Any high-risk results should always be discussed with your healthcare provider.
Who should consider NIPT?
NIPT may be suitable for:
Women who are 10 weeks pregnant or beyond
First-time mothers seeking additional reassurance
Women aged 35 years and older
Twin pregnancies (depending on eligibility)
Pregnancies with family history concerns
Parents who want early genetic insights
Anyone looking for a safer alternative to invasive testing
Who should consider NIPT?
NIPT may be suitable for:
Women who are 10 weeks pregnant or beyond
First-time mothers seeking additional reassurance
Women aged 35 years and older
Twin pregnancies (depending on eligibility)
Pregnancies with family history concerns
Parents who want early genetic insights
Anyone looking for a safer alternative to invasive testing
How does NIPT work?
Simple. Safe. Reassuring.
The NIPT process is designed to be straightforward from booking to final report release.
Book Your Test
Schedule your appointment online or through our specialist team.
Blood Sample Collection
A simple maternal blood sample is collected. No fasting is required.
Laboratory Analysis
Advanced sequencing technology analyzes DNA fragments circulating in your bloodstream.
Receive Your Results
Your confidential report is released securely in around 10-15 working days.
What can NIPT screen for?
NIFTY
Common Autosomal Trisomies
- Trisomy 21 (Down syndrome)
- Trisomy 18 (Edwards syndrome)
- Trisomy 13 (Patau syndrome)
Rare Autosomal Trisomies
- Trisomy 9
- Trisomy 16
- Trisomy 22
Incidental findings*
- Other autosomal aneuploidies
Sex Indication*
- Y chromosome detection
NIFTY Pro
Common Autosomal Trisomies
- Trisomy 21 (Down syndrome)
- Trisomy 18 (Edwards syndrome)
- Trisomy 13 (Patau syndrome)
Rare Autosomal Trisomies
- Trisomy 9
- Trisomy 16
- Trisomy 22
Sex Chromosome Aneuploidies
- XO (Turner syndrome)
- XXY (Klinefelter syndrome)
- XXX (Triple-X syndrome)
- XYY (Jacobs syndrome)
92/10 micro deletion/duplication, including:
- DiGeorge syndrome (22q11.2 deletion)
- 1p36 deletion syndrome
- Prader-Willi/Angelman syndrome
- Smith-Magenis syndrome
- Cri-du-Chat syndrome
- 4p16.3 deletion syndrome
- Distal 18q deletion syndrome
- 18p deletion syndrome
- 9p deletion syndrome
- Jacobsen Syndrome
Incidental findings
- Other autosomal aneuploidies & ≥5Mb CNVs
Sex Indication*
- Y chromosome detection
Early Answers
Get valuable insights as early as 10 weeks into pregnancy.
Why parents choose NIPT
Early answers with a safe, convenient process
NIPT provides early answers, greater reassurance, and trusted science to help families make confident decisions throughout pregnancy.
Safe & Non-Invasive
No needles into the womb and no risk to your baby.
Safe, private, and confidential
Your privacy matters at every step
Every sample, report, and patient record is handled with strict confidentiality and released only to authorized individuals.
Positive Result
Higher Risk for a Chromosomal Condition
Your results suggest an increased likelihood of the condition screened. Your doctor may recommend additional testing to confirm the result and discuss the next steps.
Negative Result
Low Risk for a Chromosomal Condition
Your results indicate a low likelihood of the conditions screened. Most patients receive negative results, providing reassurance throughout pregnancy.
Compassionate support
Safe, private, and confidential care you can trust.
We understand that pregnancy is a deeply personal experience. Our team is here to support you with professionalism, compassion, and care every step of the way.
Strictly confidential process
Released only to authorized individuals
Professional and compassionate support
Trusted end-to-end patient care
Why choose NIFTY by BGI Genomics?
Global science, trusted standards, local support
NIFTY is one of the world's pioneering NIPT technologies and has been helping families globally since 2010. BGI Genomics is a global leader in genomics and precision medicine, trusted by healthcare professionals worldwide.
One of the world's largest genomics organizations
Millions of NIPT samples processed globally
International presence across numerous countries
Advanced sequencing technology
Multiple internationally recognized quality systems
Trusted science with nationwide accessibility.
Combined with Lablog's local support and nationwide accessibility, families receive a seamless and trusted testing experience.
ISO-certified partner laboratory
Collection centers nationwide
Mobile home service in selected areas
Frequently Asked Questions
Take the next step with confidence.
Book your NIPT today and get earlier answers for your pregnancy journey.
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