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Items: 1 to 20 of 477

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7093904copy number variation1nstd102humanUncertain significance GRCh37 chr10: 99,344,461-105,992,004 , GRCh38.p12 chr10: 97,584,704-104,232,246 ABCC2, LBX1-AS1, 160 more genes
    nsv7073837inversion1nstd229human GRCh38 chr10: 99,876,246-99,883,809 , GRCh37.p13 chr10: 101,636,003-101,643,566 DNMBP
    nsv7059886inversion1nstd229human GRCh38 chr10: 95,520,399-102,687,169 , GRCh37.p13 chr10: 97,280,156-104,446,926 , ENTPD1-AS1, 168 more genes
    nsv6897044copy number variation1nstd229human GRCh38 chr10: 99,918,350-99,918,381 , GRCh37.p13 chr10: 101,678,107-101,678,138 DNMBP
    nsv6895916copy number variation1nstd229human GRCh38 chr10: 99,831,125-99,888,845 , GRCh37.p13 chr10: 101,590,882-101,648,602 DNMBP, ABCC2
    nsv6891598copy number variation1nstd229human GRCh38 chr10: 100,006,739-100,006,774 , GRCh37.p13 chr10: 101,766,496-101,766,531 DNMBP
    nsv6890920copy number variation1nstd229human GRCh38 chr10: 100,004,001-100,006,884 , GRCh37.p13 chr10: 101,763,758-101,766,641 DNMBP
    nsv6890445copy number variation1nstd229human GRCh38 chr10: 99,870,106-99,876,687 , GRCh37.p13 chr10: 101,629,863-101,636,444 DNMBP
    nsv6890158copy number variation1nstd229human GRCh38 chr10: 99,911,678-99,911,773 , GRCh37.p13 chr10: 101,671,435-101,671,530 DNMBP
    nsv6889050copy number variation1nstd229human GRCh38 chr10: 99,870,867-99,885,164 , GRCh37.p13 chr10: 101,630,624-101,644,921 DNMBP
    nsv6884878copy number variation1nstd229human GRCh38 chr10: 99,991,898-99,994,489 , GRCh37.p13 chr10: 101,751,655-101,754,246 DNMBP
    nsv6883351copy number variation1nstd229human GRCh38 chr10: 99,870,766-99,874,378 , GRCh37.p13 chr10: 101,630,523-101,634,135 DNMBP
    nsv6881952copy number variation1nstd229human GRCh38 chr10: 99,876,797-99,876,901 , GRCh37.p13 chr10: 101,636,554-101,636,658 DNMBP
    nsv6881426copy number variation1nstd229human GRCh38 chr10: 99,870,001-99,876,700 , GRCh37.p13 chr10: 101,629,758-101,636,457 DNMBP
    nsv6880968copy number variation1nstd229human GRCh38 chr10: 99,932,376-100,009,584 , GRCh37.p13 chr10: 101,692,133-101,769,341 DNMBP-AS1, DNMBP
    nsv6880127copy number variation1nstd229human GRCh38 chr10: 99,711,540-100,023,720 , GRCh37.p13 chr10: 101,471,297-101,783,477 NANOGP6, ENTPD7, 5 more genes
    nsv6879071copy number variation1nstd229human GRCh38 chr10: 99,913,275-99,917,580 , GRCh37.p13 chr10: 101,673,032-101,677,337 DNMBP
    nsv6878812copy number variation1nstd229human GRCh38 chr10: 99,859,701-99,915,200 , GRCh37.p13 chr10: 101,619,458-101,674,957 DNMBP
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