Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
OnkoRisk Hereditary Oncology Plus Panel BioReference Health United States | 97 | 77 |
|
LZTR1 Gene Noonan syndrome type 10 NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
|
Cardiomyopathy and Arrhythmia Panel Mayo Clinic Laboratories Mayo Clinic United States | 73 | 105 |
|
Comprehensive Cardiomyopathy Panel Mayo Clinic Laboratories Mayo Clinic United States | 68 | 83 |
|
Congenital Heart Disease Gene Panel Mayo Clinic Laboratories Mayo Clinic United States | 22 | 44 |
|
Hypertrophic Cardiomyopathy Panel Mayo Clinic Laboratories Mayo Clinic United States | 44 | 48 |
|
Noonan Syndrome and Related Panel Mayo Clinic Laboratories Mayo Clinic United States | 15 | 20 |
|
Hereditary Expanded Cancer Panel Mayo Clinic Laboratories Mayo Clinic United States | 1 | 86 |
|
Tempus Labs, Inc. United States | 2 | 646 |
|
Schwannomatosis Panel on Tumor Block UAB Medical Genomics Laboratory UAB Medicine United States | 2 | 3 |
|
UAB Medical Genomics Laboratory UAB Medicine United States | 8 | 18 |
|
UAB Medical Genomics Laboratory UAB Medicine United States | 7 | 17 |
|
Clinical Genomics Unit Hospital Universitari Germans Trias i Pujol Spain | 5 | 16 |
|
Clinical Genomics Unit Hospital Universitari Germans Trias i Pujol Spain | 9 | 19 |
|
FAMILIAL SCHWANNOMATOSI - SMARCB1/INI1 gene Clinical Genomics Unit Hospital Universitari Germans Trias i Pujol Spain | 2 | 3 |
|
NEUROFIBROMATOSI DE TYPE 2 - NF2 gene Clinical Genomics Unit Hospital Universitari Germans Trias i Pujol Spain | 3 | 3 |
|
Molecular Genetics Laboratory North York General Hospital Canada | 3 | 3 |
|
Comprehensive cancer panel (76 genes) Molecular Genetics Laboratory North York General Hospital Canada | 1 | 74 |
|
Molecular Genetics Laboratory North York General Hospital Canada | 19 | 20 |
|
Invitae Expanded Renal Disease Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 693 | 388 |
|
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.