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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075189inversion1nstd229human GRCh38 chr13: 38,938,572-45,892,931 , GRCh37.p13 chr13: 39,512,709-46,467,066 TPT1-AS1, AKAP11, 136 more genes
    nsv7073451inversion1nstd229human GRCh38 chr13: 39,843,646-49,674,098 , GRCh37.p13 chr13: 40,417,783-50,248,234 CYCSP34, FNDC3A, 195 more genes
    nsv7062514inversion1nstd229human GRCh38 chr13: 45,123,278-45,123,870 , GRCh37.p13 chr13: 45,697,413-45,698,005 GTF2F2, RN7SKP4
    nsv6956246copy number variation1nstd229human GRCh38 chr13: 45,120,801-45,123,762 , GRCh37.p13 chr13: 45,694,936-45,697,897 RN7SKP4, GTF2F2
    nsv6955740copy number variation1nstd229human GRCh38 chr13: 45,180,295-45,285,422 , GRCh37.p13 chr13: 45,754,430-45,859,557 GTF2F2, KCTD4, 1 more genes
    nsv6954866copy number variation1nstd229human GRCh38 chr13: 45,129,499-45,135,548 , GRCh37.p13 chr13: 45,703,634-45,709,683 GTF2F2
    nsv6953438copy number variation1nstd229human GRCh38 chr13: 44,798,553-45,795,183 , GRCh37.p13 chr13: 45,372,689-46,369,318 AKR1B1P4, KCTD4, 31 more genes
    nsv6952520copy number variation1nstd229human GRCh38 chr13: 45,181,601-45,185,400 , GRCh37.p13 chr13: 45,755,736-45,759,535 GTF2F2
    nsv6952483copy number variation1nstd229human GRCh38 chr13: 41,848,658-47,157,739 , GRCh37.p13 chr13: 42,422,794-47,731,874 TSC22D1-AS1, LINC00330, 105 more genes
    nsv6951969copy number variation1nstd229human GRCh38 chr13: 45,143,357-52,624,108 , GRCh37.p13 chr13: 45,717,492-53,198,243 SNRPGP14, EBPL, 158 more genes
    nsv6950903copy number variation1nstd229human GRCh38 chr13: 45,167,452-45,170,601 , GRCh37.p13 chr13: 45,741,587-45,744,736 GTF2F2
    nsv6950124copy number variation1nstd229human GRCh38 chr13: 45,214,725-45,214,976 , GRCh37.p13 chr13: 45,788,860-45,789,111 GTF2F2
    nsv6949537copy number variation1nstd229human GRCh38 chr13: 45,238,632-45,246,499 , GRCh37.p13 chr13: 45,812,767-45,820,634 GTF2F2, LOC105370190
    nsv6949291copy number variation1nstd229human GRCh38 chr13: 45,222,401-45,226,200 , GRCh37.p13 chr13: 45,796,536-45,800,335 LOC105370190, GTF2F2
    nsv6948649copy number variation1nstd229human GRCh38 chr13: 45,229,611-45,237,011 , GRCh37.p13 chr13: 45,803,746-45,811,146 GTF2F2, LOC105370190
    nsv6948633copy number variation1nstd229human GRCh38 chr13: 45,036,674-45,470,148 , GRCh37.p13 chr13: 45,610,809-46,044,283 RN7SKP3, LOC101929259, 17 more genes
    nsv6948435copy number variation1nstd229human GRCh38 chr13: 45,123,510-45,130,605 , GRCh37.p13 chr13: 45,697,645-45,704,740 GTF2F2, RN7SKP4
    nsv6948295copy number variation1nstd229human GRCh38 chr13: 45,180,901-45,186,700 , GRCh37.p13 chr13: 45,755,036-45,760,835 GTF2F2
    nsv6948110copy number variation1nstd229human GRCh38 chr13: 45,059,321-45,128,566 , GRCh37.p13 chr13: 45,633,456-45,702,701 GTF2F2, LOC107984596, 3 more genes
    nsv6946133copy number variation1nstd229human GRCh38 chr13: 45,159,200-45,163,588 , GRCh37.p13 chr13: 45,733,335-45,737,723 GTF2F2
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