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Results: 1 to 20 of 20
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Centogene US, LLC - The Rare Disease Company United States | 110 | 112 |
|
ANO6 - NGS including CNV analysis Centogene US, LLC - The Rare Disease Company United States | 1 | 1 |
|
ANO6 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 110 | 112 |
|
Invitae Inborn Errors of Immunity and Cytopenias Panel Invitae United States | 755 | 562 |
|
Invitae Inherited Platelet Disorders Including Thrombocytopenia Panel Invitae United States | 70 | 50 |
|
Platelet Function Disorder Panel Versiti Diagnostic Laboratories Versiti, Inc United States | 40 | 41 |
|
Platelet bleeding disorders Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 31 | 34 |
|
Platelet bleeding disorders Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 31 | 34 |
|
Scott Syndrome via the ANO6 Gene PreventionGenetics United States | 1 | 1 |
|
PreventionGenetics United States | 55 | 61 |
|
Inherited Platelet Function Disorder Panel PreventionGenetics United States | 21 | 25 |
|
Comprehensive Bleeding Disorder Panel Versiti Diagnostic Laboratories Versiti, Inc United States | 80 | 50 |
|
ANO6 Deletion/duplication analysis Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States | 1 | 1 |
|
Versiti Diagnostic Laboratories Versiti, Inc United States | 1 | 1 |
|
Comprehensive Platelet Disorder Panel Versiti Diagnostic Laboratories Versiti, Inc United States | 60 | 63 |
|
Fulgent Genetics United States | 74 | 44 |
|
Comprehensive Thrombosis, Platelet Disorder, and Coagulation Deficiency NGS Panel Fulgent Genetics United States | 146 | 82 |
|
Fulgent Genetics United States | 1 | 1 |
|
Fulgent Genetics United States | 5132 | 4672 |
|
Results: 1 to 20 of 20
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.