Clinical and research tests for C3151206 - Genetic Testing Registry (GTR)

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Results: 21 to 40 of 42

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
TULP1-Associated Disorders via the TULP1 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
Leber's congenital amaurosis panel. NGS panel of 26 genes. Genologica Medica Spain	40	26	C Sequence analysis of the entire coding region
Retinitis pigmentosa panel Genologica Medica Spain	164	108	C Sequence analysis of the entire coding region
Retinal dystrophy panel. 260 gene NGS panel. Genologica Medica Spain	420	257	C Sequence analysis of the entire coding region
TULP1 Institute for Human Genetics University Medical Center Freiburg Germany	2	1	C Sequence analysis of the entire coding region
Leber congenital amaurosis: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada	25	19	C Sequence analysis of the entire coding region
Retinopathy and Optic Atrophy NGS Panel Fulgent Genetics United States	563	241	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Leber Congenital Amaurosis , Panel Massive Sequencong (NGS) 17 Genes Reference Laboratory Genetics Spain	17	17	C Sequence analysis of the entire coding region
Leber Congenital Amaurosis NGS Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States	23	24	C Sequence analysis of the entire coding region
Cone-Rod Dystrophy NGS Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States	45	37	C Sequence analysis of the entire coding region
LEBER CONGENITAL AMAUROSIS Laboratorio de Genetica Clinica SL Spain	16	17	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Single gene testing TUPL1 CeGaT GmbH Germany	2	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
Leber congenital amaurosis panel Molecular Vision Laboratory United States	43	23	C Sequence analysis of the entire coding region
Retinal Dystrophy Panel Molecular Vision Laboratory United States	372	283	C Sequence analysis of the entire coding region
Leber Congenital Amaurosis Panel CeGaT GmbH Germany	17	20	C Sequence analysis of the entire coding region
TULP1 Single Gene Fulgent Genetics United States	2	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Clinical Exome Fulgent Genetics United States	5127	4672	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Retinitis Pigmentosa NGS Panel Fulgent Genetics United States	329	124	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Comprehensive Eye Disorders NGS Panel Fulgent Genetics United States	1018	459	D Deletion/duplication analysis C Sequence analysis of the entire coding region

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Results: 21 to 40 of 42

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.

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Results: 21 to 40 of 42

Results: 21 to 40 of 42