Non-Invasive Prenatal Testing (NIPT)
LOVE AT FIRST SIGHT
[AS EARLY AS 10 WEEKS WITH 99.9% ACCURACY]
NIPT Test | $475
Early Genetic Screening
Non-Invasive Prenatal Screening Test
EarlyReveal NIPT is available to expecting moms, including those with high-risk pregnancies, members of the general obstetric population (low risk), and those carrying singletons, twins, or who have undergone IVF. In addition to screening for trisomies 21, 18, and 13, NIPT can also detect a variety of other genetic conditions, offering valuable insights for expectant parents. The test has no risk of miscarriage and can be performed as early as 10 weeks into pregnancy. In addition to testing for the fetal sex, the EarlyReveal Trisomy Test also screens your pregnancy for common genetic conditions caused by extra or missing chromosomes, such as:
Trisomy 21 (Down syndrome)
Trisomy 18 (Edwards syndrome)
Trisomy 13 (Patau syndrome)
Sex chromosome aneuploidies:
Monosomy X (Turner syndrome)
XXY syndrome (Klinefelter syndrome)
Trisomy X (Triple X syndrome)
XYY syndrome (Jacobs syndrome)
*NIPS is a screening test; screen-positive (high-risk) results should be confirmed through diagnostic testing.
Covered by the majority of Collective Insurance
Our whole genome sequencing approach delivers highly reliable results, identifying common trisomies and microdeletions with a proven track record in clinical validation of >99% accuracy.
Unmatched Accuracy
EarlyReveal NIPT offers over 99% accuracy and a lower failure rate than other tests, reducing the chances of inconclusive results or the need for a second sample collection.
Highest Standards
Testing is available as early as 10 weeks into your pregnancy and is conducted by our in-house nurse, ensuring a safe, sterile, and professional sample collection in a comfortable environment.
Flexible
Once your sample is returned to our laboratory, you'll receive fast results in as little as 3 to 5 business days.
Fast & Convenient
Discover Peace of Mind
Every pregnancy is unique, and our non-invasive prenatal testing (NIPT) is designed to provide expectant parents and healthcare providers with valuable insights into fetal health. Trusted by health care professionals across Canada, our advanced screening technology analyses fetal DNA from a simple maternal blood sample, allowing early detection of potential genetic conditions.
Screening Performance
EarlyReveal™ trisomy test is performed on the world most advanced and recognized sequencing platform and has been evaluated for clinical performance in multiple studies, inclusive of >60 000 total venous and capillary samples*. Based on this data, expected failure rate is extremely low and the performance is >99% sensitivity and >99.9% specificity for trisomy 21, 18, and 13.
Most extended health insurance plans cover Non-Invasive Prenatal Testing (NIPT) either partially or in full. We recommend checking with your insurance provider to confirm your coverage before booking. When speaking with them, ask if genetic screening or prenatal testing is included in your plan and whether a doctor’s requisition is required for reimbursement.
If your insurance covers NIPT, you will typically pay upfront and submit a claim for reimbursement. We are happy to provide detailed receipts and documentation to assist with the process.
Insurance & Coverage for NIPT Testing
Choose between our NIPT Tests
Detects Common Genetic Conditions with High Accuracy
Simple, Quick, and Stress-Free
Choosing the right NIPT test depends on the level of screening you need. A standard NIPT screens for the most common chromosomal conditions, while a comprehensive test includes additional screening for rarer genetic conditions. Before booking, speak with your healthcare provider to determine the best option for you and ensure your requisition form is completed prior to your appointment. If needed, we are happy to fax it on your behalf.
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Trisomy 21 (Down syndrome)
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Trisomy 18 (Edwards syndrome)
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Trisomy 13 (Patau syndrome)
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V Sex Chromomose Aneuploidies:
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Monosomy X (Turner syndrome)
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XXY syndrome (Klinefelter syndrome)
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Trisomy X (Triple X syndrome)
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XYY syndrome (Jacobs syndrome)
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Over 99.9% accurate
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Fast Turnaround: 3-5 business day
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Safe for Mom and Baby
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Only 1 blood collection tube required.
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As early as 10 weeks into pregnancy
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Baby's sex available at no cost
NIPT | $475
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Trisomy 21 (Down syndrome)
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Trisomy 18 (Edwards syndrome
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Trisomy 13 (Patau syndrome)
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Sex Chromomose Aneuploidies:
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Monosomy X (Turner syndrome)
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XXY syndrome (Klinefelter syndrome)
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Trisomy X (Triple X syndrome)
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XYY syndrome (Jacobs syndrome)
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V
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Trisomy of ALL chromosomes.
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Microdeletion 1p36
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Microdeletion 4p-(Wolf-Hirschhorn syndrome)
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Microdeletion 5p- (cri-du-chat syndrome)
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Microdeletion15q11.2 (Prader-Willi
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syndrome/Angelman syndrome)
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Microdeletion22q11.2 (DiGeorge)
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Over 99.9% accurate
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Fast Turnaround: 3-5 business day
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Safe for Mom and Baby
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Only 1 blood collection tube required.
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As early as 10 weeks into pregnancy
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Baby's sex available at no extra cost
NIPT + | $600
How to Make an Informed Decision About NIPT
Deciding whether to undergo Non-Invasive Prenatal Testing (NIPT) is a personal choice that depends on your unique pregnancy journey. To make an informed decision, consider discussing the benefits and limitations of the test with your healthcare provider. Ask about what the results can and cannot tell you, how they may impact your next steps, and whether additional testing would be needed in certain cases. Understanding your family history, risk factors, and personal preferences will help you determine if NIPT is the right choice for you. Knowledge empowers you—take the time to explore your options and make the best decision for your pregnancy.
