Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Retinal dystrophy panel. 260 gene NGS panel. Genologica Medica Spain | 420 | 257 |
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Genomic Unity® Custom Analysis Variantyx, Inc. United States | 1 | 4054 |
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Prenatal Known Familial Mutation GeneDx United States | 1 | 1716 |
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Custom XomeDxSlice (2-150 Genes, Proband Only) GeneDx United States | 1 | 1718 |
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GeneDx United States | 1 | 1040 |
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Two Known Familial Variants in a Nuclear Gene GeneDx United States | 1 | 1043 |
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One Known Familial Variant in a Nuclear Gene GeneDx United States | 1 | 1045 |
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NewbornDx Advanced Sequencing Evaluation Athena Diagnostics United States | 1 | 1722 |
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Night blindness, congenital stationary: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 14 | 13 |
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Congenital Stationary Night Blindness NGS Panel Fulgent Genetics United States | 27 | 17 |
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Retinopathy and Optic Atrophy NGS Panel Fulgent Genetics United States | 563 | 241 |
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Congenital Stationary Night Blindness (CSNB) NGS Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States | 17 | 15 |
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NIGHT BLINDNESS, CONGENITAL STATIONARY (X-LINKED) Laboratorio de Genetica Clinica SL Spain | 2 | 2 |
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Blueprint Genetics Finland | 1 | 260 |
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Congenital Stationary Night Blindness Panel Blueprint Genetics Finland | 1 | 17 |
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Fulgent Genetics United States | 3 | 1 |
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CeGaT GmbH Germany | 1 | 1 |
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Congenital Stationary Night Blindness panel Molecular Vision Laboratory United States | 19 | 14 |
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Molecular Vision Laboratory United States | 372 | 283 |
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Congenital Stationary Night Blindness Panel CeGaT GmbH Germany | 6 | 15 |
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