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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976816inversion1nstd209human GRCh38 chr11: 102,182,065-102,183,846 , GRCh37.p13 chr11: 102,052,796-102,054,577 YAP1
    nsv5975769insertion1nstd209human GRCh38 chr11: 102,228,634-102,228,634 , GRCh37.p13 chr11: 102,099,365-102,099,365 YAP1
    nsv5915038copy number variation1nstd209human GRCh38 chr11: 102,174,582-102,180,681 , GRCh37.p13 chr11: 102,045,313-102,051,412 YAP1
    nsv5907615copy number variation1nstd209human GRCh38 chr11: 102,150,729-102,151,399 , GRCh37.p13 chr11: 102,021,460-102,022,130 YAP1
    nsv5860444copy number variation1nstd209human GRCh38 chr11: 102,174,594-102,180,293 , GRCh37.p13 chr11: 102,045,325-102,051,024 YAP1
    nsv5699444mobile element insertion1nstd211human GRCh38 chr11: 102,182,578-102,182,578 , GRCh37.p13 chr11: 102,053,309-102,053,309 YAP1
    nsv5672640copy number variation1nstd102humanPathogenic GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976 HSPD1P13, CARD17P, 239 more genes
    nsv5562279inversion1nstd206human GRCh38 chr11: 102,182,052-102,183,887 , GRCh37.p13 chr11: 102,052,783-102,054,618 YAP1
    nsv5556869sequence alteration1nstd206human GRCh38 chr11: 102,182,108-102,183,928 , GRCh37.p13 chr11: 102,052,839-102,054,659 YAP1
    nsv5511437copy number variation1nstd206human GRCh38 chr11: 102,174,595-102,180,682 , GRCh37.p13 chr11: 102,045,326-102,051,413 YAP1
    nsv5507725copy number variation1nstd206human GRCh38 chr11: 102,233,895-102,236,735 , GRCh37.p13 chr11: 102,104,626-102,107,466 YAP1
    nsv5503494copy number variation1nstd206human GRCh38 chr11: 102,192,909-102,192,963 , GRCh37.p13 chr11: 102,063,640-102,063,694 YAP1
    nsv5499372copy number variation1nstd206human GRCh38 chr11: 102,110,339-102,110,405 , GRCh37.p13 chr11: 101,981,070-101,981,136 YAP1
    nsv5496758copy number variation1nstd206human GRCh38 chr11: 102,178,931-102,179,368 , GRCh37.p13 chr11: 102,049,662-102,050,099 YAP1
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5373833translocation1nstd200human GRCh38 chr11: 102,180,669-102,180,669 , GRCh38 chr11: 102,174,595-102,174,595 , GRCh37.p13 chr11: 102,051,400-102,051,400 , GRCh37.p13 chr11: 102,045,326-102,045,326 YAP1
    nsv5355468translocation1nstd200human GRCh38 chr22: 32,476,677-32,476,677 , GRCh38 chr11: 102,110,637-102,110,637 , GRCh37.p13 chr11: 101,981,368-101,981,368 , GRCh37.p13 chr22: 32,872,664-32,872,664 YAP1, FBXO7
    nsv5339273translocation1nstd200human GRCh37 chr11: 102,063,694-102,063,694 , GRCh37 chr11: 102,063,640-102,063,640 , GRCh38.p12 chr11: 102,192,963-102,192,963 , GRCh38.p12 chr11: 102,192,909-102,192,909 YAP1
    nsv5313687copy number variation1nstd204human GRCh38.p13 chr11: 102,174,586-102,180,678 , GRCh37.p13 chr11: 102,045,317-102,051,409 YAP1
    nsv5309043copy number variation1nstd204human GRCh38.p13 chr11: 102,150,175-102,150,997 , GRCh37.p13 chr11: 102,020,906-102,021,728 YAP1
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