Invitae

Analyzes genes associated with hereditary cardiovascular conditions that, if detected early, may have effective medical interventions and preventive m...

Tests 424 genes related to cerebral palsy.

A genetic test used to identify chromosomal abnormalities.

Analyzes genes that have the potential to improve public health, as defined by the CDC's Office of Public Health Genomics.

Helps patients consider clinical trials.

Patients can schedule an individual post-test counseling session at no additional charge.

Aid in interpreting results.

Provide result-specific insights regarding variants, genes and conditions.

Provides sponsored, no-charge genetic testing and counseling for individuals suspected of having a lysosomal storage disease.

Analyzes genes selected by The Electronic Medical Records and Genomics (eMERGE) Genomic Risk Assessment and Management Network.

Tests up to 320 genes related to epilepsy.

A genetic counseling session is available at no additional cost to patients located in the US, US territories, and Canada who have ordered a currently...

Available to answer brief questions about genetic testing and results, included at no additional cost for patients in the US, US territories, and Cana...

Invitae's genetic counselors provide peer-to-peer support to healthcare providers and post-test counseling to patients who have received certain Invit...

Carrier screening is recommended especially for hereditary cancers.

A session included at no additional cost for those with Invitae results to discuss genetic test results and health implications.

Comprehensive next-generation sequencing (NGS) testing performed in our CLIA/CAP-certified labs enables diagnoses, informed family planning, and proac...

Looks at more than 167 genes to assess your employees’ risk of developing an inherited form of cancer or cardiovascular (heart) disease—and more.

Comprehensive genetic information for patients with rare diseases to inform prognosis, treatments, and next steps.

Identify gene-specific information including published management guidelines, relevant studies and patient resources.

Empowering people to make decisions about their health through the power of genetics.

Genetic risk evaluation is recommended when there is a history of certain cancers.

Supports Invitae’s mission to make testing more accessible to patients who may have a hereditary condition by reducing financial barriers and streamli...

A powerful tool to improve health by finding a medical diagnosis for unexplained symptoms, confirming a suspected disease, discovering new treatment o...

Identifies women who may have hereditary health risks and need additional care.

Analyzes genes identified as medically actionable by the American College of Medical Genetics and Genomics.

Analyzes genes associated with Charcot-Marie-Tooth disease (CMT), characterized by progressive muscle weakness and sensory loss in arms and legs.

Tests 92 genes related to connective tissue disorders.

Analyzes genes associated with hereditary conditions that, if detected early, may have effective medical interventions and preventive measures.

Genetic testing for the 3 genes most commonly associated with hereditary Alzheimer’s disease.

Analyzes genes associated with hereditary motor neuropathy (HMN), characterized by loss of motor neurons leading to weakness and muscle wasting.

Analyzes genes associated with hereditary sensory and autonomic neuropathy (HSAN) and hereditary sensory neuropathy (HSN).

Analyzes genes associated with hereditary spastic paraplegia (HSP), characterized by lower-extremity spastic weakness.

Tests up to 241 genes for conditions affecting neurodevelopment.

Provides genetic insights to help guide treatment decisions and identify at-risk family members who may benefit from genetic testing.

Tests 358 genes associated with skeletal disorders.

Genetic testing for up to two genes associated with small fiber neuropathy (SFNP).

Analyzes the copy number of two genes: SMN1, which is associated with spinal muscular atrophy (SMA), and SMN2, which modifies the clinical phenotype.

Medical-grade genetic testing can help inform some of the most important health decisions in your patients’ lives. Invitae makes ordering a test and i...

Offers healthy adults an opportunity to learn about how their genes could potentially impact their health. Enables proactive monitoring or preventive ...

Patients who harbor hereditary variants could benefit from tailored management for different cancer types.

Consult with a genetics expert.

Tests up to 474 genes related to primary immunodeficiency.

This package includes genetic tests recommended for patients with conditions that impair cognitive and/or social functioning. Offers actionable insigh...

Tests up to 230 genes related to neuromuscular disorders.

Analyzes genes associated with hereditary neuropathies, including Charcot-Marie-Tooth disease (CMT), hereditary motor neuropathy (HMN), etc.

Identifies patients and family members who are at higher risk for some disorders.

Starts a personalized health plan for heart disease, cancer, and more based on unique genetic information.

Manages and promotes programs for patients who may benefit from genetic testing; may bill insurance or provide testing at no charge.

Analyzes genes associated with conditions that may have surgery-related clinical implications.

Request a test online via a telehealth clinician or work with your doctor.

Differentiate between genetic tests so you can select the one that’s best for your patient.