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Results: 1 to 20 of 20
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Invitae Expanded Renal Disease Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 693 | 388 |
|
Centogene AG - the Rare Disease Company Germany | 316 | 314 |
|
PKHD1 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 498 | 498 |
|
Centogene AG - the Rare Disease Company Germany | 499 | 499 |
|
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 |
|
Invitae Cystic Kidney Disease Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 96 | 44 |
|
PreventionGenetics, part of Exact Sciences United States | 130 | 69 |
|
Invitae Progressive Renal Disease Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 310 | 195 |
|
Invitae Broad Carrier Screen without X-linked Disorders Labcorp Genetics (formerly Invitae) LabCorp United States | 195 | 98 |
|
Labcorp Genetics (formerly Invitae) LabCorp United States | 224 | 112 |
|
Invitae Comprehensive Carrier Screen Labcorp Genetics (formerly Invitae) LabCorp United States | 886 | 547 |
|
Polycystic kidney disease panel. NGS panel of 10 genes. Genologica Medica Spain | 17 | 10 |
|
Ciliopathy panel. NGS panel of 99 genes. Genologica Medica Spain | 152 | 97 |
|
Congenital liver fibrosis panel. NGS panel of 52 genes. Genologica Medica Spain | 89 | 50 |
|
PKHD1 Deletion/duplication analysis Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States | 1 | 1 |
|
HNL Genomics Connective Tissue Gene Tests United States | 44 | 45 |
|
Results: 1 to 20 of 20
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.