Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Molecular Vision Laboratory United States | 1358 | 1028 |
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PRCD - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
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Centogene AG - the Rare Disease Company Germany | 417 | 413 |
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Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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qGenEx Intellectual disability Quantitative Genomic Medicine Laboratories, SL Spain | 3 | 1969 |
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Invitae Inherited Retinal Disorders Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 486 | 293 |
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Invitae Comprehensive Carrier Screen Labcorp Genetics (formerly Invitae) LabCorp United States | 886 | 547 |
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Retinitis Pigmentosa, autosomal recessive and X-linked Amplexa Genetics Amplexa Genetics A/S Denmark | 2 | 65 |
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Molecular Vision Laboratory United States | 342 | 268 |
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Autosomal Recessive Retinitis Pigmentosa 36 (RP36) via the PRCD Gene PreventionGenetics, part of Exact Sciences United States | 1 | 1 |
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PreventionGenetics, part of Exact Sciences United States | 91 | 82 |
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Autosomal Recessive Retinitis Pigmentosa (RP) Panel PreventionGenetics, part of Exact Sciences United States | 62 | 60 |
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Genomic Unity® Retinal Disorders Analysis Variantyx, Inc. United States | 1 | 394 |
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CGC Genetics Unilabs Portugal | 1 | 203 |
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CGC Genetics Unilabs Portugal | 1 | 306 |
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CGC Genetics Unilabs Portugal | 1 | 223 |
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Diseases of the posterior ocular segment (WES based NGS panel of 307 gene, including CNV analysis) CGC Genetics Unilabs Portugal | 1 | 307 |
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Retinitis pigmentosa 36 (sequence analysis of PRCD gene) CGC Genetics Unilabs Portugal | 1 | 1 |
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Integrated Genetics Westborough LabCorp United States | 330 | 746 |
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Targeted Variant, Fetal Analysis Integrated Genetics Westborough LabCorp United States | 292 | 746 |
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