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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4405480copy number variation1nstd174human GRCh37 chr8: 42,919,717-42,921,810 , GRCh38.p12 chr8: 43,064,574-43,066,667 FNTA
    esv3617025copy number variation104estd214human GRCh37 chr8: 42,920,582-42,921,613 , GRCh38.p12 chr8: 43,065,439-43,066,470 FNTA

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