Filters
reset allOther countries
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Molecular Genetics Laboratory London Health Sciences Centre Canada | 15 | 15 |
|
Centogene US, LLC - The Rare Disease Company United States | 195 | 221 |
|
HJV - NGS including CNV analysis Centogene US, LLC - The Rare Disease Company United States | 1 | 1 |
|
Centogene US, LLC - The Rare Disease Company United States | 316 | 314 |
|
Centogene US, LLC - The Rare Disease Company United States | 669 | 688 |
|
Centogene AG - the Rare Disease Company Germany | 195 | 221 |
|
Centogene AG - the Rare Disease Company Germany | 316 | 314 |
|
HJV - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 669 | 688 |
|
Invitae Iron Related Disorders Panel Invitae United States | 39 | 27 |
|
Hemochromatosis, type 2A, 602390, Autosomal recessive; HFE2A (Hemochromatosis type 2) (MLPA) Intergen Genetic Diagnosis and Research Centre Turkey | 1 | 1 |
|
Invitae Comprehensive Carrier Screen without X-linked Disorders Invitae United States | 228 | 279 |
|
Invitae Comprehensive Carrier Screen Invitae United States | 247 | 301 |
|
Hereditary Hemochromatosis Panel PreventionGenetics United States | 7 | 7 |
|
Juvenile Hereditary Hemochromatosis via the HFE2 (HJV) Gene PreventionGenetics United States | 1 | 1 |
|
Invitae Hereditary Hemochromatosis Panel Invitae United States | 11 | 6 |
|
Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders Germany | 1 | 1 |
|
Hereditary Hemochromatosis Panel Blueprint Genetics Finland | 7 | 5 |
|
HFE2 Gene Sequencing and Deletion/Duplication Analysis DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children United States | 1 | 1 |
|
Hemochromatosis NGS and Deletion and Duplication Panel DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children United States | 15 | 7 |
|
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.