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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5704466mobile element insertion1nstd211human GRCh38 chr12: 80,717,694-80,717,694 , GRCh37.p13 chr12: 81,111,473-81,111,473 MYF5
    nsv5500934copy number variation1nstd206human GRCh38 chr12: 76,069,603-82,449,398 , GRCh37.p13 chr12: 76,463,383-82,843,177 , E2F7, 65 more genes
    nsv5124406mobile element insertion1nstd203human GRCh38 chr12: 80,716,751-80,716,765 , GRCh37.p13 chr12: 81,110,530-81,110,544 MYF5
    nsv5037136inversion1nstd200human GRCh38 chr12: 69,787,024-109,882,221 , GRCh37.p13 chr12: 70,180,804-110,320,026 , RPL23AP68, 540 more genes
    nsv5036282inversion1nstd200human GRCh38 chr12: 52,338,357-95,425,642 , GRCh37.p13 chr12: 52,732,141-95,819,418 , MIR6502, 769 more genes
    nsv5032581inversion1nstd200human GRCh38 chr12: 67,763,754-90,678,993 , GRCh37.p13 chr12: 68,157,534-91,072,770 , LOC105369886, 255 more genes
    nsv4888823inversion1nstd200human GRCh37 chr12: 68,157,543-91,072,771 , GRCh38.p12 chr12: 67,763,763-90,678,994 , BEST3, 255 more genes
    nsv4886161inversion1nstd200human GRCh37 chr12: 70,180,810-110,320,027 , GRCh38.p12 chr12: 69,787,030-109,882,222 , LOC728739, 540 more genes
    nsv4883504inversion1nstd200human GRCh37 chr12: 52,732,141-95,819,418 , GRCh38.p12 chr12: 52,338,357-95,425,642 , MYL6B, 769 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
    nsv4675559copy number variation1nstd102humanUncertain significance GRCh37 chr12: 79,302,790-82,128,250 , GRCh38.p12 chr12: 78,909,010-81,734,471 NOP56P3, PPP1R12A-AS2, 31 more genes
    nsv4611334copy number variation1nstd183human GRCh37 chr12: 81,113,217-81,122,440 , GRCh38.p12 chr12: 80,719,438-80,728,661 MYF5
    nsv4516210mobile element insertion1nstd166human GRCh37.p13 chr12: 81,110,530-81,110,530 , GRCh38.p12 chr12: 80,716,751-80,716,751 MYF5
    nsv4456763copy number variation1nstd102humanPathogenic GRCh37 chr12: 77,737,623-94,330,526 , GRCh38.p12 chr12: 77,343,843-93,936,750 MIR1252, PLEKHG7, 162 more genes
    nsv4365518copy number variation1nstd173human GRCh37 chr12: 80,725,347-81,268,996 , GRCh38.p12 chr12: 80,331,567-80,875,217 LOC105369867, MIR617, 9 more genes
    nsv4345788sequence alteration1nstd166human GRCh37.p13 chr12: 59,785,153-101,478,055 , GRCh38.p12 chr12: 59,391,372-101,084,277 , APAF1, 538 more genes
    nsv4325802inversion1nstd166human GRCh37.p13 chr12: 70,180,810-110,320,028 , GRCh38.p12 chr12: 69,787,030-109,882,223 , APAF1, 540 more genes
    nsv4324772inversion1nstd166human GRCh37.p13 chr12: 27,368,635-91,765,744 , GRCh38.p12 chr12: 27,215,702-91,371,967 , ATP2B1, 1101 more genes
    nsv4216511copy number variation1nstd166human GRCh37.p13 chr12: 80,896,476-81,200,737 , GRCh38.p12 chr12: 80,502,697-80,806,958 MYF5, MYF6, 5 more genes
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