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Items: 2

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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4426786copy number variation1nstd174human GRCh37 chr9: 123,255,123-123,260,688 , GRCh38.p12 chr9: 120,492,845-120,498,410 CDK5RAP2
    esv2663480copy number variation449estd199human GRCh37 chr9: 123,257,024-123,259,730 , GRCh38.p12 chr9: 120,494,746-120,497,452 CDK5RAP2

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