Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Ovarian cancer, somatic, 167000 (CTNNB1 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Ovarian cancer, somatic, 167000 (OPCML gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Ovarian cancer, somatic, 167000 (Exon 4) (AKT1 gene) (Sequence Analysis) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Ovarian carcinoma, somatic, 167000 (CDH1 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
QDx Pathology Services, Inc. United States | 15 | 44 |
|
Clariti Diagnostics Laboratories LLC United States | 15 | 44 |
|
OnkoRisk Hereditary Oncology Plus Panel BioReference Health United States | 97 | 77 |
|
OnkoRisk Hereditary Oncology Management Panel BioReference Health United States | 47 | 17 |
|
OnkoRisk Women's Hereditary Cancer Panel BioReference Health United States | 34 | 18 |
|
OnkoRisk Hereditary Urology Panel BioReference Health United States | 27 | 19 |
|
Myriad Genetics, Inc. United States | 1 | 2 |
|
Myriad Genetics, Inc. United States | 6 | 2 |
|
Hereditary Colon and Endometrial Cancer-ColoNGS GeneKor MSA Greece | 10 | 7 |
|
Hereditary Non-Polyposis Colorectal Cancer (HNPCC) or Lynch Syndrome GeneKor MSA Greece | 7 | 5 |
|
Tier 1 Hereditary Conditions Test Color Diagnostics, LLC DBA Color Health United States | 14 | 10 |
|
Molecular Vision Laboratory United States | 1358 | 1028 |
|
Centogene AG - the Rare Disease Company Germany | 218 | 135 |
|
CTNNB1 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 6 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 3 | 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.