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Results: 1 to 17 of 17
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Invitae Corneal Dystrophies Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 65 | 33 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
PreventionGenetics, part of Exact Sciences United States | 40 | 27 |
|
Gelatinous Drop-Like Corneal Dystrophy (GDLD) via the TACSTD2 Gene PreventionGenetics, part of Exact Sciences United States | 1 | 1 |
|
Hereditary amyloidosis (WES based NGS panel of 21 genes, including CNV analysis) CGC Genetics Unilabs Portugal | 1 | 21 |
|
Mendelics Brazil | 1 | 28 |
|
HEREDITARY AMYLOIDOSIS SYNDROME PANEL Laboratorio de Genetica Clinica SL Spain | 1 | 22 |
|
Corneal dystrophy panel. NGS panel of 27 genes. Genologica Medica Spain | 44 | 27 |
|
Genologica Medica Spain | 44 | 19 |
|
Corneal dystrophy: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 19 | 11 |
|
Genomic Unity® Custom Analysis Variantyx, Inc. United States | 1 | 4054 |
|
Fulgent Genetics United States | 47 | 24 |
|
Blueprint Genetics Finland | 1 | 27 |
|
MGZ Medical Genetics Center Germany | 6 | 167 |
|
Fulgent Genetics United States | 1 | 1 |
|
Fulgent Genetics United States | 5128 | 4672 |
|
Comprehensive Eye Disorders NGS Panel Fulgent Genetics United States | 1018 | 459 |
|
Results: 1 to 17 of 17
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.