Clinical and research tests for C3151001 - Genetic Testing Registry (GTR)

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Results: 21 to 40 of 47

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Mottled Retinal Disorders Panel. 12-gene NGS panel. Genologica Medica Spain	25	12	C Sequence analysis of the entire coding region
RHO Institute for Human Genetics University Medical Center Freiburg Germany	3	1	C Sequence analysis of the entire coding region
Retinitis pigmentosa: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada	75	71	C Sequence analysis of the entire coding region
Congenital Stationary Night Blindness NGS Panel Fulgent Genetics United States	27	17	D Deletion/duplication analysis 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
Flecked Retina NGS Panel Fulgent Genetics United States	28	14	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Retinitis Pigmentosa (Complet Panel) , Panel Massive Sequencing (NGS) 57 Genes Reference Laboratory Genetics Spain	57	57	C Sequence analysis of the entire coding region
Autosomal Dominant Retinitis Pigmentosa, Panel Massive Sequencing (NGS) 27 Genes Reference Laboratory Genetics Spain	26	27	C Sequence analysis of the entire coding region
Autosomal Recessive and Sporadic Retinitis Pigmentosa, Panel Massive Sequencing (NGS) 41 Genes Reference Laboratory Genetics Spain	41	41	C Sequence analysis of the entire coding region
RETINITIS PIGMENTOSA (AUTOSOMAL DOMINANT) Laboratorio de Genetica Clinica SL Spain	7	7	X Mutation scanning of select exons C Sequence analysis of the entire coding region
Retinitis Pigmentosa NGS Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States	103	92	C Sequence analysis of the entire coding region
Retinitis Pigmentosa , Sequencing RHO Gene Reference Laboratory Genetics 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
Single gene testing RHO CeGaT GmbH Germany	3	1	C Sequence analysis of the entire coding region
Congenital Stationary Night Blindness panel Molecular Vision Laboratory United States	19	14	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
Retinitis pigmentosa, autosomal recessive and X-linked Panel CeGaT GmbH Germany	37	62	C Sequence analysis of the entire coding region
Retinitis pigmentosa, autosomal dominant and X-linked Panel CeGaT GmbH Germany	24	30	C Sequence analysis of the entire coding region
RHO Institute of Human Genetics Medical University Innsbruck Austria	3	1	S Mutation scanning of the entire coding region
RHO Fulgent Genetics United States	3	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region

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Results: 21 to 40 of 47

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 47

Results: 21 to 40 of 47