Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Noonan Syndrome and Related Panel Mayo Clinic Laboratories Mayo Clinic United States | 15 | 20 |
|
Medical Genomics Laboratory Department of Genetics UAB United States | 8 | 18 |
|
Medical Genomics Laboratory Department of Genetics UAB United States | 7 | 17 |
|
Health in Code Spain | 26 | 12 |
|
Clinical Genomics Unit Hospital Universitari Germans Trias i Pujol Spain | 5 | 16 |
|
Clinical Genomics Unit Hospital Universitari Germans Trias i Pujol Spain | 9 | 19 |
|
Invitae Expanded Renal Disease Panel Invitae United States | 693 | 388 |
|
Comprehensive HemeComplete Profile + Heme Fusion + CALR PCR + FLT3 PCR PathGroup United States | 16 | 160 |
|
UCSF Molecular Diagnostics Laboratory UCSF Molecular Diagnostics Laboratory University of California, San Francisco United States | 4 | 52 |
|
Centogene AG - the Rare Disease Company Germany | 114 | 68 |
|
Centogene AG - the Rare Disease Company Germany | 156 | 107 |
|
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 | 5 | 1 |
|
NF1 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 5 | 1 |
|
PTPN11 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 4 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 1886 | 1858 |
|
Bone Marrow Failure / Anemia Panel Centogene AG - the Rare Disease Company Germany | 212 | 212 |
|
Centogene AG - the Rare Disease Company Germany | 289 | 275 |
|
Centogene AG - the Rare Disease Company Germany | 740 | 728 |
|
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.