Clinical and research tests for 6935 - Genetic Testing Registry (GTR) - NCBI

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Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Invitae Corneal Dystrophies Panel Invitae United States	65	33	D Deletion/duplication analysis
Corneal dystrophy, posterior polymorphous, 3, 609141; PPCD3 (Posterior polymorphous corneal dystrophy) (ZEB1 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Corneal dystrophy, Fuchs endothelial, 6, 613270; FECD6 (Fuchs endothelial corneal dystrophy) (ZEB1 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Anterior Segment Dysgenesis Disorders Panel PreventionGenetics, part of Exact Sciences United States	272	278	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
ZEB1-Associated Corneal Dystrophies via the ZEB1 Gene PreventionGenetics, part of Exact Sciences United States	2	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Corneal Dystrophies Panel PreventionGenetics, part of Exact Sciences United States	40	27	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
MitoMet®Plus aCGH Analysis Baylor Genetics United States	842	637	D Deletion/duplication analysis
Corneal Diseases Panel Mendelics Brazil	1	28	C Sequence analysis of the entire coding region
Corneal dystrophy panel. NGS panel of 27 genes. Genologica Medica Spain	44	27	C Sequence analysis of the entire coding region
Corneal dystrophy: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada	18	10	C Sequence analysis of the entire coding region
Genomic Unity® Custom Analysis Variantyx, Inc. United States	1	4054	D Deletion/duplication analysis X Mutation scanning of select exons C Sequence analysis of the entire coding region
Retinal Dystrophy Xpanded Panel GeneDx United States	20	856	C Sequence analysis of the entire coding region
ZEB1 Institute for Human Genetics University Medical Center Freiburg Germany	2	1	C Sequence analysis of the entire coding region
Corneal Dystrophy NGS Panel Fulgent Genetics United States	47	24	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Posterior Polymorphous Corneal Dystrophy , Panel Massive Sequencing (NGS) OVOL2, COL8A2, ZEB1 Reference Laboratory Genetics Spain	3	3	C Sequence analysis of the entire coding region
Corneal Dystrophy , Panel Massive Sequencing (NGS) 18 Genes Reference Laboratory Genetics Spain	27	18	C Sequence analysis of the entire coding region
POSTERIOR POLYMORPHOUS CORNEAL DYSTROPHY Laboratorio de Genetica Clinica SL Spain	1	1	C Sequence analysis of the entire coding region
Eye diseases comprehensive panel Asper Biogene Asper Biogene LLC Estonia	367	291	C Sequence analysis of the entire coding region
Corneal Dystrophy Panel Blueprint Genetics Finland	1	27	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Eye Diseases - panels MGZ Medical Genetics Center Germany	6	167	D Deletion/duplication analysis C Sequence analysis of the entire coding region

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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.