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Genetic insights can
change everything

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  • New data suggest current guidelines miss patients who could benefit from testing. Learn more.
  • Out-of-pocket cost estimates for HBOC and Lynch testing now available. Learn more.
  • Sponsored genetic testing available for spinal muscular atrophy (SMA). Learn more.

Explore our genetic test catalog

Diagnostics

Confirm a diagnosis, provide a better understanding of prognosis, and direct medical management

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Reproductive health

Help make healthy pregnancies possible with carrier screening and preimplantation testing

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Proactive health

Determine a healthy adult’s predisposition to cancer, cardiovascular conditions, and more

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The Invitae Network makes genetic information more powerful

The Invitae Network creates data-driven connections throughout the healthcare system to advance research and care.

  • Removes barriers to genetic testing to help patients receive an accurate diagnosis quicker
  • Provides information to researchers and biopharma companies to help bring new therapies to market sooner
  • Supports newly diagnosed patients and their clinicians in making decisions on next steps, including treatments, clinical trials, and research

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Transparent pricing.
Ethical billing.

Panel testing that lets you take cost out of the equation with no explanation of benefits >$1500 ever.

A genetic diagnosis can affect an entire family


Only a small percentage of relatives pursue genetic testing after a disease-causing variant is found in their family, even though guidelines recommend it.1-3

Invitae now offers testing for all panels to first-degree family members at no additional charge* to help inform and empower more families.

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*Order must be placed within 90 days of the original report

1. Christiaans I, et al. Update of genetic counseling and predictive DNA testing in hypertrophic cardiomyopathy. Eur J Hum Genet. 2008;16(10):1201-7.
2. Sharaf RN, et al. Uptake of genetic testing by relatives of Lynch syndrome probands: A systematic review. Clin Gastroenterol Hepatol. 2013;11(9):1093-100.
3. Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®) for Genetic/Familial High-Risk Assessment: Breast and Ovarian V.2.2017. © National Comprehensive Cancer Network, Inc 2016. All rights reserved. Accessed September 25, 2017. To view the most recent and complete version of the guideline, go online to NCCN.org.  NCCN makes no warranties of any kind whatsoever regarding their content, use or application and disclaims any responsibility for their application or use in any way.

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