Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Expedio Hereditary Cancer Predisposition Screening Assay Kailos Genetics United States | 40 | 31 |
|
OnkoRisk Hereditary Oncology Plus Panel BioReference Health United States | 97 | 77 |
|
OnkoRisk Hereditary Oncology Guideline Panel BioReference Health United States | 71 | 54 |
|
OnkoRisk Women's Hereditary Cancer Panel BioReference Health United States | 34 | 18 |
|
GeneID Lab - Advanced Molecular Diagnostics United States | 60 | 34 |
|
Genetic Pathology SA Pathology Australia | 3 | 1 |
|
Hereditary pheochromocytoma and paraganglioma panel (12 genes) Molecular Genetics Laboratory North York General Hospital Canada | 8 | 12 |
|
Invitae Expanded Renal Disease Panel Invitae United States | 691 | 388 |
|
Molecular Vision Laboratory United States | 1357 | 1028 |
|
Common Hereditary Cancer Screening Panel PreventionGenetics, part of Exact Sciences United States | 94 | 55 |
|
Centogene AG - the Rare Disease Company Germany | 67 | 33 |
|
Centogene AG - the Rare Disease Company Germany | 113 | 68 |
|
Centogene AG - the Rare Disease Company Germany | 155 | 107 |
|
Centogene AG - the Rare Disease Company Germany | 218 | 135 |
|
Centogene AG - the Rare Disease Company Germany | 5 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 4 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 4 | 1 |
|
KIF1B - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 3 | 1 |
|
RET - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 5 | 1 |
|
SDHB - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 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.