Access comprehensive genetic tests easily and confidently
Our tests are developed and delivered by leaders in specialty testing to help you transform data into personal health insights. Labcorp's nationwide network of conveniently located patient service centers makes sample collection easy.
across 15 clinical specialty areas
offering a diverse set of clinical data
advancing genetic science and breakthroughs
supporting both patients and clinicians
Genetic insights advance healthcare
Providers
From oncology and women’s health to neurology and rare disease, Labcorp can support you and your patients’ genetic testing needs throughout the continuum of care.
Individuals & Patients
With genetic testing supported by genetic counseling, we can help you understand the options that may be best for you.
Biopharma
We collaborate with hundreds of scientists and researchers from biotech and pharmaceutical companies to help you test, validate and bring to market your next pharmaceutical or medical device product.
Commercial Partnerships
Through our capabilities in specialty testing, high-value datasets and global footprint, Labcorp can scale to meet your commercial needs for genetic testing.
Expanding the impact of genetic data
genetic tests performed
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Expertise that moves genetics forward
Our combined industry leadership includes Labcorp’s 50+ years in global life sciences and Invitae’s innovative, proven approach to genetic testing and ethical data sharing.
Broad access that benefits more people
Our 6,500+ tests (including genetic tests) are covered by most health plans, and patient samples can be collected at patient service centers nationwide—making genetic testing more accessible and available than ever.
Support that drives confident decisions
Our dedicated customer service team and genetic counselors can help you and your patients understand test results and decide on potential next steps.
Featured genetic tests
Cell-free DNA (cfDNA) screening
MaterniT 21 PLUS is an early pregnancy risk assessment that screens for Down syndrome and other chromosomal abnormalities that could affect baby’s health and development.
Epilepsy-related testing
A full suite of epilepsy testing to help clarify diagnosis and prognosis, support optimal treatment selection and assess epilepsy drug levels in patients.
Comprehensive solid tumor genomic and immune profiling test
An advanced, solid tumor NGS test that supports personalized care by gaining a deeper understanding of the tumor and its microenvironment.
Myeloid malignancy testing
An NGS-based assay that detects somatic variants in patients with myeloid malignancies, offering insights for diagnosis, prognosis and treatment.
Hear from patients
Stories
“It’s something that’s going to affect us forever, but we’re so grateful to finally have an answer. We’ve been able to connect with several other families affected by the condition, and it’s been very helpful.”
Stories
“I’m not too worried about my future. Getting genetic testing helped because now we have a plan and understand my risks better.”
Stories
“The results gave us the insight we needed and helped us focus our concern on what was really happening with Meaghen. The news was painful, but it allowed us to adapt to that pain. It improved Meaghen’s quality of life, which should be the ultimate goal.”
Stories
“I know my mom missed out on special moments with her own mother, like shopping for wedding dresses and enjoying her grandchildren. As a mother of three children, I want to know my cancer risks so I can be there for my family and those important moments.”
Questions? We’re here to help.
Our team is available to answer questions and guide you—whether you’re a patient, provider, health plan, payer or otherwise.
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