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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5729521mobile element insertion1nstd211human GRCh38 chr12: 56,711,041-56,711,041 , GRCh37.p13 chr12: 57,104,825-57,104,825 NACA
    nsv5597499copy number variation1nstd207human GRCh38 chr12: 56,718,096-56,718,164 , GRCh37.p13 chr12: 57,111,880-57,111,948 NACA
    nsv5588031copy number variation1nstd207human GRCh38 chr12: 56,717,735-56,717,803 , GRCh37.p13 chr12: 57,111,519-57,111,587 NACA
    nsv5562355mobile element insertion1nstd206human GRCh38 chr12: 56,711,041-56,711,092 , GRCh37.p13 chr12: 57,104,825-57,104,876 NACA
    nsv5510862copy number variation1nstd206human GRCh38 chr12: 56,717,367-56,718,406 , GRCh37.p13 chr12: 57,111,151-57,112,190 NACA
    nsv5508476copy number variation1nstd206human GRCh38 chr12: 56,717,035-56,717,192 , GRCh37.p13 chr12: 57,110,819-57,110,976 NACA
    nsv5310148copy number variation1nstd204human GRCh38.p13 chr12: 56,717,864-56,718,638 , GRCh37.p13 chr12: 57,111,648-57,112,422 NACA
    nsv5270364copy number variation1nstd204human GRCh38.p13 chr12: 56,716,901-56,725,000 , GRCh37.p13 chr12: 57,110,685-57,118,784 NACA
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv5036282inversion1nstd200human GRCh38 chr12: 52,338,357-95,425,642 , GRCh37.p13 chr12: 52,732,141-95,819,418 , MIR6502, 769 more genes
    nsv4972896copy number variation1nstd200human GRCh38 chr12: 56,707,127-56,710,605 , GRCh37.p13 chr12: 57,100,911-57,104,389 NACA
    nsv4883504inversion1nstd200human GRCh37 chr12: 52,732,141-95,819,418 , GRCh38.p12 chr12: 52,338,357-95,425,642 , MYL6B, 769 more genes
    nsv4845754copy number variation1nstd200human GRCh37 chr12: 57,111,745-57,112,293 , GRCh38.p12 chr12: 56,717,961-56,718,509 NACA
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4740683copy number variation1nstd199human GRCh37 chr12: 57,111,887-57,111,956 , GRCh38.p12 chr12: 56,718,103-56,718,172 NACA
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4675143copy number variation1nstd102humanPathogenic GRCh37 chr12: 55,552,371-62,126,304 , GRCh38.p12 chr12: 55,158,587-61,732,523 OR6C71P, METTL1, 183 more genes
    nsv4606859copy number variation1nstd183human GRCh37 chr12: 57,110,564-57,115,506 , GRCh38.p12 chr12: 56,716,780-56,721,722 NACA
    nsv4576151mobile element insertion1nstd166human GRCh37.p13 chr12: 57,104,816-57,104,816 , GRCh38.p12 chr12: 56,711,032-56,711,032 NACA
    nsv4569165sequence alteration1nstd166human GRCh37.p13 chr12: 57,109,905-57,111,893 , GRCh38.p12 chr12: 56,716,121-56,718,109 NACA
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