Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Genetic Services Laboratory University of Chicago United States | 16 | 16 |
|
Joubert/Meckel-Gruber syndrome Panel Genetic Services Laboratory University of Chicago United States | 34 | 41 |
|
NPHP3 Gene Nephronophthisis type 3 NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
|
Cystic Kidney Disease Gene Panel Mayo Clinic Laboratories Mayo Clinic United States | 16 | 44 |
|
Invitae Expanded Renal Disease Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 693 | 388 |
|
Molecular Vision Laboratory United States | 1358 | 1028 |
|
Centogene AG - the Rare Disease Company Germany | 243 | 238 |
|
NPHP3 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 3 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 1886 | 1858 |
|
Centogene AG - the Rare Disease Company Germany | 777 | 770 |
|
Centogene AG - the Rare Disease Company Germany | 498 | 498 |
|
Centogene AG - the Rare Disease Company Germany | 417 | 413 |
|
Centogene AG - the Rare Disease Company Germany | 499 | 499 |
|
Centogene AG - the Rare Disease Company Germany | 247 | 262 |
|
Centogene AG - the Rare Disease Company Germany | 740 | 728 |
|
Centogene AG - the Rare Disease Company Germany | 829 | 848 |
|
Invitae Nephronophthisis Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 54 | 27 |
|
Labcorp Genetics (formerly Invitae) LabCorp United States | 210 | 134 |
|
Mayo Clinic Laboratories Mayo Clinic United States | 7 | 112 |
|
Invitae Limb and Digital Malformations Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 356 | 177 |
|
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.