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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5501401copy number variation1nstd206human GRCh38 chr12: 52,321,487-52,321,934 , GRCh37.p13 chr12: 52,715,271-52,715,718 KRT83
    nsv5498104copy number variation1nstd206human GRCh38 chr12: 52,294,714-52,389,423 , GRCh37.p13 chr12: 52,688,498-52,783,207 KRT84, KRT83, 3 more genes
    nsv5319636copy number variation1nstd204human GRCh38.p13 chr12: 52,294,704-52,389,432 , GRCh37.p13 chr12: 52,688,488-52,783,216 KRT83, KRT86, 3 more genes
    nsv5272049copy number variation1nstd204human GRCh38.p13 chr12: 52,294,701-52,389,500 , GRCh37.p13 chr12: 52,688,485-52,783,284 KRT89P, KRT83, 3 more genes
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv4985600copy number variation1nstd200human GRCh38 chr12: 52,294,714-52,389,423 , GRCh37.p13 chr12: 52,688,498-52,783,207 KRT85, KRT89P, 3 more genes
    nsv4847735copy number variation1nstd200human GRCh37 chr12: 52,688,498-52,783,207 , GRCh38.p12 chr12: 52,294,714-52,389,423 KRT83, KRT85, 3 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4615207copy number variation1nstd183human GRCh37 chr12: 52,706,564-52,707,158 , GRCh38.p12 chr12: 52,312,780-52,313,374 KRT83
    nsv4614464copy number variation1nstd183human GRCh37 chr12: 52,682,239-52,779,578 , GRCh38.p12 chr12: 52,288,455-52,385,794 KRT81, KRT83, 4 more genes
    nsv4609389copy number variation1nstd183human GRCh37 chr12: 52,715,633-52,717,673 , GRCh38.p12 chr12: 52,321,849-52,323,889 KRT83
    nsv4607735copy number variation1nstd183human GRCh37 chr12: 52,685,772-52,785,519 , GRCh38.p12 chr12: 52,291,988-52,391,735 KRT81, KRT83, 4 more genes
    nsv4604675copy number variation1nstd183human GRCh37 chr12: 52,688,684-52,721,236 , GRCh38.p12 chr12: 52,294,900-52,327,452 KRT86, KRT83
    nsv4602355copy number variation2nstd183human GRCh37 chr12: 52,681,150-52,783,493 , GRCh38.p12 chr12: 52,287,366-52,389,709 KRT81, KRT83, 4 more genes
    nsv4599141copy number variation1nstd183human GRCh37 chr12: 52,706,564-52,707,818 , GRCh38.p12 chr12: 52,312,780-52,314,034 KRT83
    nsv4559196inversion1nstd166human GRCh37.p13 chr12: 51,569,865-55,219,228 , GRCh38.p12 chr12: 51,176,082-54,825,444 , EIF4B, 163 more genes
    nsv4423600copy number variation1nstd174human GRCh37 chr12: 52,706,564-52,708,420 , GRCh38.p12 chr12: 52,312,780-52,314,636 KRT83
    nsv4414276copy number variation1nstd174human GRCh37 chr12: 52,678,900-52,788,039 , GRCh38.p12 chr12: 52,285,116-52,394,255 KRT81, KRT82, 5 more genes
    nsv4388507copy number variation3nstd173human GRCh37 chr12: 52,688,601-52,781,851 , GRCh38.p12 chr12: 52,294,817-52,388,067 KRT86, KRT83, 3 more genes
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