Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Personalis, Inc. United States | 1 | 269 |
|
Genetic Services Laboratory University of Chicago United States | 72 | 133 |
|
Genetic Services Laboratory University of Chicago United States | 13 | 24 |
|
CREBBP Gene Rubinstein-Taybi syndrome NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
|
Comprehensive Nephrology Gene Panel Mayo Clinic Laboratories Mayo Clinic United States | 1 | 299 |
|
Microdeletion / Microduplication Syndromes Molecular Genetics and Cytogenetics, Clinical Laboratory Service RED DE SALUD UC CHRISTUS Chile | 28 | 39 |
|
High-Resolution Rapid Microarray (CGH and SNP) Allele Diagnostics United States | 247 | 231 |
|
Tempus Labs, Inc. United States | 2 | 647 |
|
Congenital heart diseases Panel Health in Code Spain | 1 | 76 |
|
Cardiovascular Diseases_General Panel Health in Code Spain | 1 | 380 |
|
Foundation Medicine, Inc. United States | 2 | 405 |
|
Rapid microarray (CGH and SNP) Allele Diagnostics United States | 247 | 231 |
|
Invitae Expanded Renal Disease Panel Invitae United States | 693 | 388 |
|
OnkoSight Advanced Bladder Cancer Panel BioReference Health United States | 1 | 39 |
|
Comprehensive HemeComplete Profile + Heme Fusion + CALR PCR + FLT3 PCR PathGroup United States | 16 | 160 |
|
Centogene AG - the Rare Disease Company Germany | 243 | 238 |
|
CREBBP - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 2 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 218 | 135 |
|
Centogene AG - the Rare Disease Company Germany | 74 | 34 |
|
Centogene AG - the Rare Disease Company Germany | 1886 | 1858 |
|
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.