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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074199inversion1nstd229human GRCh38 chr12: 123,186,434-132,825,682 , GRCh37.p13 chr12: 123,670,981-133,402,268 PIWIL1, FZD10-AS1, 187 more genes
    nsv7073519inversion1nstd229human GRCh38 chr12: 126,711,147-127,123,265 , GRCh37.p13 chr12: 127,195,693-127,607,810 LINC00944, LOC105370061, 8 more genes
    nsv7062773inversion1nstd229human GRCh38 chr12: 126,641,790-126,744,586 , GRCh37.p13 chr12: 127,126,336-127,229,132 LINC00944, LINC02824, 2 more genes
    nsv6936274copy number variation1nstd229human GRCh38 chr12: 126,767,591-126,853,252 , GRCh37.p13 chr12: 127,252,137-127,337,798 LINC00944
    nsv6936199copy number variation1nstd229human GRCh38 chr12: 126,389,353-126,747,623 , GRCh37.p13 chr12: 126,873,899-127,232,169 LINC02825, LOC100996671, 10 more genes
    nsv6934942copy number variation1nstd229human GRCh38 chr12: 126,635,621-127,113,411 , GRCh37.p13 chr12: 127,120,167-127,597,956 LOC105370063, LINC00943, 9 more genes
    nsv6933362copy number variation1nstd229human GRCh38 chr12: 126,697,987-127,393,083 , GRCh37.p13 chr12: 127,182,533-127,877,628 LOC107984450, LINC02372, 15 more genes
    nsv6932916copy number variation1nstd229human GRCh38 chr12: 126,478,201-126,993,600 , GRCh37.p13 chr12: 126,962,747-127,478,145 LOC105370061, LINC00944, 11 more genes
    nsv6929584copy number variation1nstd229human GRCh38 chr12: 126,761,752-126,761,950 , GRCh37.p13 chr12: 127,246,298-127,246,496 LINC00944
    nsv6926450copy number variation1nstd229human GRCh38 chr12: 126,730,176-126,732,668 , GRCh37.p13 chr12: 127,214,722-127,217,214 LINC00944
    nsv6926331copy number variation1nstd229human GRCh38 chr12: 126,728,988-126,729,132 , GRCh37.p13 chr12: 127,213,534-127,213,678 LINC00944
    nsv6926174copy number variation1nstd229human GRCh38 chr12: 126,267,752-127,405,138 , GRCh37.p13 chr12: 126,752,298-127,889,683 LINC00943, LOC100996671, 26 more genes
    nsv6925203copy number variation1nstd229human GRCh38 chr12: 126,323,462-127,334,182 , GRCh37.p13 chr12: 126,808,008-127,818,727 LOC100996671, PGBD3P3, 26 more genes
    nsv6924289copy number variation1nstd229human GRCh38 chr12: 126,719,889-126,758,431 , GRCh37.p13 chr12: 127,204,435-127,242,977 LINC00943, LINC00944, 1 more genes
    nsv6924270copy number variation1nstd229human GRCh38 chr12: 126,572,659-126,843,187 , GRCh37.p13 chr12: 127,057,205-127,327,733 LOC100996671, LINC00943, 2 more genes
    nsv6921911copy number variation1nstd229human GRCh38 chr12: 126,765,650-126,765,855 , GRCh37.p13 chr12: 127,250,196-127,250,401 LINC00944
    nsv6920058copy number variation1nstd229human GRCh38 chr12: 126,734,597-126,734,786 , GRCh37.p13 chr12: 127,219,143-127,219,332 LINC00944
    nsv6493151copy number variation1nstd223human GRCh38 chr12: 126,635,621-127,113,411 , GRCh37.p13 chr12: 127,120,167-127,597,956 LINC00944, HSPE1P20, 9 more genes
    nsv6492805copy number variation1nstd223human GRCh38 chr12: 126,389,353-126,747,623 , GRCh37.p13 chr12: 126,873,899-127,232,169 FAM32EP, LINC02347, 10 more genes
    nsv6492488copy number variation1nstd223human GRCh38 chr12: 126,501,475-128,016,495 , GRCh37.p13 chr12: 126,986,021-128,501,040 LOC105370061, LOC105370064, 29 more genes
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