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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093395copy number variation1nstd102humanPathogenic GRCh37 chr12: 64,609,458-70,352,103 , GRCh38.p12 chr12: 64,215,678-69,958,323 TODL, MIR6074, 116 more genes
    nsv7076483inversion1nstd229human GRCh38 chr12: 64,360,164-64,367,784 , GRCh37.p13 chr12: 64,753,944-64,761,564 C12orf56
    nsv7071931inversion1nstd229human GRCh38 chr12: 55,156,710-64,781,897 , GRCh37.p13 chr12: 55,550,494-65,175,677 ZBTB39, MIR548Z, 236 more genes
    nsv7069614inversion1nstd229human GRCh38 chr12: 57,953,160-64,335,038 , GRCh37.p13 chr12: 58,346,943-64,728,818 LOC100419700, LOC105369793, 67 more genes
    nsv7069192inversion1nstd229human GRCh38 chr12: 60,220,562-64,985,387 , GRCh37.p13 chr12: 60,614,343-65,379,167 KLF17P1, DPY19L2, 60 more genes
    nsv7066910inversion1nstd229human GRCh38 chr12: 60,203,453-65,465,649 , GRCh37.p13 chr12: 60,597,234-65,859,429 RPS11P6, MSRB3-AS1, 68 more genes
    nsv7064501inversion1nstd229human GRCh38 chr12: 60,432,939-65,464,484 , GRCh37.p13 chr12: 60,826,720-65,858,264 RSL24D1P5, RASSF3, 66 more genes
    nsv7063625inversion1nstd229human GRCh38 chr12: 60,220,582-64,980,713 , GRCh37.p13 chr12: 60,614,363-65,374,493 RASSF3, RPS27P24, 60 more genes
    nsv7062231inversion1nstd229human GRCh38 chr12: 62,212,375-66,047,637 , GRCh37.p13 chr12: 62,606,156-66,441,417 GAPDHP44, C12orf56, 73 more genes
    nsv7059707inversion1nstd229human GRCh38 chr12: 63,145,635-65,964,303 , GRCh37.p13 chr12: 63,539,415-66,358,083 LOC100418730, LEMD3, 52 more genes
    nsv7058808inversion1nstd229human GRCh38 chr12: 57,953,150-64,330,730 , GRCh37.p13 chr12: 58,346,933-64,724,510 LOC105369786, ATP23, 67 more genes
    nsv6930831copy number variation1nstd229human GRCh38 chr12: 64,338,701-64,342,100 , GRCh37.p13 chr12: 64,732,481-64,735,880 ATP6V1E1P3, C12orf56
    nsv6926779copy number variation1nstd229human GRCh38 chr12: 64,352,439-64,356,057 , GRCh37.p13 chr12: 64,746,219-64,749,837 C12orf56
    nsv6925434copy number variation1nstd229human GRCh38 chr12: 64,388,529-64,395,226 , GRCh37.p13 chr12: 64,782,309-64,789,006 RPS11P6, C12orf56
    nsv6924941copy number variation1nstd229human GRCh38 chr12: 64,260,901-64,264,600 , GRCh37.p13 chr12: 64,654,681-64,658,380 C12orf56
    nsv6924541copy number variation1nstd229human GRCh38 chr12: 64,270,214-64,285,859 , GRCh37.p13 chr12: 64,663,994-64,679,639 C12orf56
    nsv6922375copy number variation1nstd229human GRCh38 chr12: 64,383,933-64,387,967 , GRCh37.p13 chr12: 64,777,713-64,781,747 C12orf56
    nsv6922332copy number variation1nstd229human GRCh38 chr12: 64,260,529-64,265,327 , GRCh37.p13 chr12: 64,654,309-64,659,107 C12orf56
    nsv6921945copy number variation1nstd229human GRCh38 chr12: 64,279,979-64,280,012 , GRCh37.p13 chr12: 64,673,759-64,673,792 C12orf56
    nsv6921195copy number variation1nstd229human GRCh38 chr12: 64,344,197-64,379,778 , GRCh37.p13 chr12: 64,737,977-64,773,558 C12orf56
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