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Items: 3

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    Number of Variants: 3

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4769250copy number variation1nstd201human GRCh37 chrX: 96,096,220-155,208,244 , GRCh38.p12 chrX: 96,841,221-155,978,579 AGTR2, ABCD1, 959 more genes
    nsv4769248copy number variation1nstd201human GRCh37 chrX: 168,546-21,870,371 , GRCh38.p12 chrX: 251,879-21,852,253 AMELX, SLC25A6, 248 more genes
    nsv4769247copy number variation1nstd201human GRCh37 chr13: 109,490,236-115,107,733 , GRCh38.p12 chr13: 108,837,888-114,342,258 PARP1P1, ATP4B, 117 more genes

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