Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Blueprint Genetics Finland | 1 | 7 |
|
Abnormal Genitalia/ Disorders of Sex Development Panel Blueprint Genetics Finland | 4 | 49 |
|
MGZ Medical Genetics Center Germany | 14 | 342 |
|
Mental Retardation and Dysmorphology - panels MGZ Medical Genetics Center Germany | 15 | 343 |
|
Invitae van der Woude Syndrome Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 2 | 2 |
|
Abnormal/Ambiguous Genitalia Panel Genetic Services Laboratory University of Chicago United States | 81 | 91 |
|
Bioarray Spain | 1 | 1 |
|
CeGaT GmbH Germany | 3 | 1 |
|
Fulgent Genetics United States | 3 | 1 |
|
Fulgent Genetics United States | 5124 | 4672 |
|
Praxis fuer Humangenetik Wien Austria | 1 | 1 |
|
Orofacial cleft 6/ Cleft lip with or without cleft palate Praxis fuer Humangenetik Wien Austria | 1 | 1 |
|
Autosomal dominant popliteal pterygium syndrome Praxis fuer Humangenetik Wien Austria | 1 | 1 |
|
Genome Diagnostics Laboratory University Medical Center Utrecht Netherlands | 1 | 1 |
|
Genome Diagnostics Laboratory University Medical Center Utrecht Netherlands | 1 | 1 |
|
Genetics Laboratory University of Oklahoma Health Sciences Center United States | 1 | 88 |
|
Center for Human Genetics Cliniques Universitaires Saint Luc Belgium | 1 | 1 |
|
Laboratory of Human Molecular Genetics de Duve Institute - Universite catholique de Louvain Belgium | 1 | 1 |
|
Laboratory of Human Molecular Genetics de Duve Institute - Universite catholique de Louvain Belgium | 1 | 1 |
|
Laboratory of Human Molecular Genetics de Duve Institute - Universite catholique de Louvain Belgium | 1 | 1 |
|
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.