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| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Holoprosencephaly Panel, Sequencing and Deletion/Duplication ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States | 8 | 8 |
|
Holoprosencephaly-5 (Autosomal Dominant, Nonsyndromic) via the ZIC2 Gene PreventionGenetics, part of Exact Sciences United States | 1 | 1 |
|
Holoprosencephaly, Autosomal Dominant, Nonsyndromic, Panel PreventionGenetics, part of Exact Sciences United States | 10 | 14 |
|
Institute for Human Genetics University Medical Center Freiburg Germany | 1 | 1 |
|
Holoprosencephaly panel. 12-gene NGS panel. Genologica Medica Spain | 27 | 12 |
|
Microphthalmia, Anophthalmia, and Coloboma Panel NGS Panel Fulgent Genetics United States | 244 | 78 |
|
Holoprosencephaly Panel, Sequencing and Deletion/Duplication, Fetal ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States | 9 | 8 |
|
Asper Biogene Asper Biogene LLC Estonia | 318 | 252 |
|
Quantitative Genomic Medicine Laboratories, SL Spain | 135 | 136 |
|
Invitae Holoprosencephaly Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 6 | 5 |
|
Epilepsy Comprehensive NGS Panel Fulgent Genetics United States | 729 | 398 |
|
Bioarray Spain | 1 | 1 |
|
CeGaT GmbH Germany | 1 | 1 |
|
CeGaT GmbH Germany | 11 | 7 |
|
CeGaT GmbH Germany | 11 | 7 |
|
Fulgent Genetics United States | 1 | 1 |
|
Fulgent Genetics United States | 13 | 7 |
|
Fulgent Genetics United States | 5128 | 4672 |
|
Intellectual Disability NGS Panel Fulgent Genetics United States | 1058 | 554 |
|
Comprehensive Eye Disorders NGS Panel Fulgent Genetics United States | 1018 | 459 |
|
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.