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| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
GENETIX Centro de Investigación en Genética Humana y Reproductiva Colombia | 2 | 1 |
|
F5 - NGS including CNV analysis Centogene US, LLC - The Rare Disease Company United States | 5 | 1 |
|
Centogene US, LLC - The Rare Disease Company United States | 218 | 135 |
|
Centogene US, LLC - The Rare Disease Company United States | 74 | 34 |
|
Centogene AG - the Rare Disease Company Germany | 218 | 135 |
|
Centogene AG - the Rare Disease Company Germany | 74 | 34 |
|
F5 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 5 | 1 |
|
Invitae Pharmacogenomics Panel Invitae United States | 43 | 37 |
|
Invitae Inborn Errors of Immunity and Cytopenias Panel Invitae United States | 755 | 562 |
|
Invitae Familial Essential Thrombocythemia Panel Invitae United States | 9 | 3 |
|
Stroke, Cerebral Hemorrhage, Hemiplegia, and Migraine Panel PreventionGenetics United States | 342 | 156 |
|
Johns Hopkins Genomics DNA Diagnostic Laboratory Johns Hopkins Hospital United States | 250 | 155 |
|
Inherited Bone Marrow Failure Panel PreventionGenetics United States | 266 | 186 |
|
Intergen Genetic Diagnosis and Research Centre Turkey | 1 | 1 |
|
Budd-Chiari syndrome, 600880, Autosomal recessive; BDCHS (Budd-Chiari syndrome) (Prenatal) (MLPA) Intergen Genetic Diagnosis and Research Centre Turkey | 1 | 1 |
|
Intergen Genetic Diagnosis and Research Centre Turkey | 1 | 1 |
|
Budd-Chiari syndrome, 600880, Autosomal recessive; BDCHS (Budd-Chiari syndrome) (MLPA) Intergen Genetic Diagnosis and Research Centre Turkey | 1 | 1 |
|
Invitae Hereditary Thrombophilia Panel Invitae United States | 24 | 11 |
|
Baylor Genetics United States | 11 | 3 |
|
Factor V Leiden Mutation Panel Baylor Genetics United States | 5 | 1 |
|
IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.