Panorama Non-Invasive Prenatal Testing (NIPT)
Panorama Non-Invasive Prenatal Testing (NIPT)
Panorama Non-Invasive Prenatal Testing (NIPT)
  1. Panorama Non-Invasive Prenatal Testing (NIPT)
  2. Panorama Non-Invasive Prenatal Testing (NIPT)
  3. Panorama Non-Invasive Prenatal Testing (NIPT)

Please print and bring the requisition to your healthcare provider for signature. Unsigned requisitions will NOT be accepted at any LifeLabs® location.
If your healthcare provider has already given you a signed paper requisition, please bring it directly to a LifeLabs® location to pay and complete your testing.

Panorama Non-Invasive Prenatal Testing (NIPT)

Panorama™ is a non-invasive test performed through a simple blood draw from the mother’s arm. Because of its unique technology, this NIPT test can distinguish between the mother and baby’s DNA and see if there is evidence of genetic conditions that could affect the baby’s health.

About Panorama™ Non-Invasive Prenatal Testing 

Who is this test for?

If you would like to know more about your baby’s health and the risk for certain genetic conditions, Panorama™ from LifeLabs Genetics® screens for extra or missing chromosomes. Suitable for single or twin pregnancies and pregnancies using an egg donor or surrogate, Panorama™ can be ordered as early as 9 weeks, giving you time to plan and prepare for your baby.

What is this test used for?

  • Basic Prenatal Panel screens for common genetic conditions such as Down Syndrome during pregnancy (as early as 9 weeks) that can impact the health of a baby. 
  • Extended Prenatal Panel screens for common genetic conditions plus 22q.11.2 (DiGeorge syndrome).
  • Full Prenatal Panel screens for common genetic conditions plus 5 microdeletions (22q.11.2 [DiGeorge syndrome], 1p36 deletion syndrome, Angelman syndrome, Cri-du-chat syndrome, Prader-Willi syndrome). 
  • Panorama™ can tell if twins are identical or fraternal, and report the sex of each fetus.

To understand more about this test click on learn more:

Basic Prenatal Panel
Trisomy 21, 18, 13, monosomy X, sex chromosome trisomies, triploidy, complete molar pregnancy and fetal sex optional.
Extended Prenatal Panel
Testing of chromosomes 21, 13, 18, X, Y, triploidy, and 22q11.2 deletion.
Full Prenatal Panel
Testing of chromosomes 21,13,18,X,Y, triploidy, 22q deletion, Cri-du-chat,1p36 deletion, Angelman, Prader-Willi.
Test Type
Blood Sample

Test Category
Reproductive Health & Pregnancy

Test Turnaround Time
Results available to ordering physician within 7-10 days

British Columbia and Ontario

Sample Collection
LifeLabs® Patient Service Centre (BC, ON, SK)
MyVisit at-home collection (ON)
All other provinces/territories please call 1-84-GENE HELP (1-844-363-4357)

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