Clinical and research tests for C1867300 - Genetic Testing Registry (GTR) - NCBI

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Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
MVL Vision Panel Molecular Vision Laboratory United States	1358	1028	C Sequence analysis of the entire coding region
Retinitis pigmentosa 9, 180104, Autosomal dominant; RP9 (Retinitis pigmentosa) (RP9 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
MVL Vision Panel Molecular Vision Laboratory United States	342	268	C Sequence analysis of the entire coding region
MitoMet®Plus aCGH Analysis Baylor Genetics United States	842	637	D Deletion/duplication analysis
Retinitis pigmentosa 9 (sequence analysis of RP9 gene) CGC Genetics Unilabs Portugal	1	1	C Sequence analysis of the entire coding region
RP9 Institute for Human Genetics University Medical Center Freiburg Germany	1	1	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
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
Retinitis Pigmentosa NGS Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States	103	92	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
RETINITIS PIGMENTOSA GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases Spain	56	57	C Sequence analysis of the entire coding region
RETINITIS PIGMENTOSA A.D GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases Spain	27	27	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 dominant and X-linked Panel CeGaT GmbH Germany	24	30	C Sequence analysis of the entire coding region
RP9 Single Gene Fulgent Genetics United States	1	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Autosomal Dominant Retinitis Pigmentosa Asper Biogene Asper Biogene LLC Estonia	25	26	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Clinical Exome Fulgent Genetics United States	5129	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
Autosomal Recessive Retinitis Pigmentosa Asper Biogene Asper Biogene LLC Estonia	57	56	C Sequence analysis of the entire coding region

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Results: 1 to 20 of 22

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.