Finding more answers for more patients, together

With your genetics expertise and Invitae’s commitment to high-quality, affordable testing, we can translate genetics into meaningfully better care and support.

Woman at a desk by a window – Genetic specialist
Invitae’s comprehensive suite of tests support and inform health decisions for over four million patients across all stages of life

Comprehensive suite of genetic tests to inform health decisions

Invitae’s tests help you deliver answers in all stages of life.

  • Diagnosis and treatment: cancer, cardiovascular disease, neurology, pediatrics, metabolic disorders & newborn screening, immunology and more
  • Healthy mom and baby: comprehensive carrier screening, non-invasive prenatal screening.
  • Healthy individuals: heritable cancer and cardiovascular risk.

Genes are personal. So are our tests.

Each patient is unique. That’s why we offer highly flexible test options, so you can customize your selection to meet the needs of every patient.

Male and female discussing genetic testing

Committed to affordability

Cost shouldn’t be a barrier to genetic information. When you order a genetic test with Invitae, you get more than just testing.

  • Through the Invitae Billing Assurance Program, our dedicated billing specialists work with each patient to get a comprehensive view of their individual situation
  • Within the US, billing insurance is often the most cost-effective choice. Invitae is in-network with national US health insurance plans and typically the out-of-pocket cost for a patient using insurance is less than $100
  • Customizable payment options based on a patient’s specific situation
Gloved hands picking up lab object

A new gold standard

Invitae’s advanced sequencing combined with a state-of-the-art variant interpretation framework yields clear, actionable and reliable results.

  • Customized molecular and bioinformatics methods means that we find variants that may be missed by other labs¹,²
  • Invitae’s functional modeling platform and Sherloc variant classification framework enable accurate variant interpretation and fewer VUS
  • Exome analysis with boosted NGS coverage of medically relevant genes includes case-level reanalysis every six months
  • RNA analysis to provide more definitive results in cancer testing
  • Ongoing contributions to ClinVar, to enable detailed peer review of variant classifications and consensus classification by the global community of experts

An ecosystem of tools, education and testing support

Invitae is more than a lab. As your partner in genetic testing, our team of specialists are here to support you so that you can help your patients make informed decisions.

References

1. Truty, R., Paul, J., Kennemer, M. et al. Prevalence and properties of intragenic copy-number variation in Mendelian disease genes. Genet Med. 2019;21:114–123. doi.org/10.1038/s41436-018-0033-5.
2. Data on file. Invitae.