Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Hereditary Paraganglioma and Pheochromocytoma Panel PreventionGenetics, part of Exact Sciences United States | 12 | 12 |
|
Hereditary Paraganglioma-Pheochromocytoma Syndrome via the SDHAF2 Gene PreventionGenetics, part of Exact Sciences United States | 1 | 1 |
|
Molecular Vision Laboratory United States | 1 | 1 |
|
Color Diagnostics, LLC DBA Color Health United States | 51 | 59 |
|
Hereditary Paraganglioma-Pheochromocytoma Expanded Panel, Sequencing and Deletion/Duplication ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States | 12 | 12 |
|
Mitochondrial genome sequencing Molecular Vision Laboratory United States | 525 | 339 |
|
Mitochondrial Panel, Nuclear genes CNH Molecular Diagnostics Laboratory Childrens National Hospital United States | 145 | 134 |
|
Paragangliomas: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 5 | 5 |
|
ACMG Secondary Findings (Medically Actionable Genes, Including Cardio and Cancer) NGS Panel Fulgent Genetics United States | 177 | 59 |
|
Oxidative Phosphorylation Disorders NGS Panel Fulgent Genetics United States | 416 | 235 |
|
PHEOCHROMOCYTOMA-PARAGANGLIOMA Laboratorio de Genetica Clinica SL Spain | 6 | 11 |
|
Comprehensive Hereditary Cancer Panel Baylor Genetics United States | 132 | 61 |
|
Hereditary Endocrine Cancer Panel Baylor Genetics United States | 51 | 15 |
|
Hereditary Paraganglioma/Pheochromocytoma Panel Baylor Genetics United States | 21 | 9 |
|
Baylor Genetics United States | 41 | 13 |
|
Invitae Pediatric Solid Tumors Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 90 | 48 |
|
CeGaT GmbH Germany | 1 | 1 |
|
Comprehensive Hereditary Cancer Panel Genetic Services Laboratory University of Chicago United States | 25 | 139 |
|
Paraganglioma-Pheochromocytoma Comprehensive Panel Fulgent Genetics United States | 29 | 11 |
|
Full Comprehensive Cancer Panel Fulgent Genetics United States | 329 | 127 |
|
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.