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Items: 1 to 20 of 125

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973218insertion1nstd209human GRCh38 chr11: 44,942,023-44,942,023 , GRCh37.p13 chr11: 44,963,574-44,963,574 TP53I11
    nsv5652774insertion1nstd207human GRCh38 chr11: 44,942,023-44,942,023 , GRCh37.p13 chr11: 44,963,574-44,963,574 TP53I11
    nsv5539780insertion1nstd206human GRCh38 chr11: 44,942,039-44,942,074 , GRCh37.p13 chr11: 44,963,590-44,963,625 TP53I11
    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
    nsv5307164copy number variation1nstd204human GRCh38.p13 chr11: 44,942,267-44,950,956 , GRCh37.p13 chr11: 44,963,818-44,972,507 TP53I11
    nsv5280036copy number variation1nstd204human GRCh38.p13 chr11: 44,941,937-44,950,751 , GRCh37.p13 chr11: 44,963,488-44,972,302 TP53I11
    nsv5273957copy number variation1nstd204human GRCh38.p13 chr11: 44,941,901-44,950,400 , GRCh37.p13 chr11: 44,963,452-44,971,951 TP53I11
    nsv5269690copy number variation1nstd204human GRCh38.p13 chr11: 44,942,001-44,952,300 , GRCh37.p13 chr11: 44,963,552-44,973,851 TP53I11
    nsv4984453copy number variation1nstd200human GRCh38 chr11: 44,942,273-44,950,951 , GRCh37.p13 chr11: 44,963,824-44,972,502 TP53I11
    nsv4846845copy number variation1nstd200human GRCh37 chr11: 44,963,824-44,972,502 , GRCh38.p12 chr11: 44,942,273-44,950,951 TP53I11
    nsv4844547copy number variation1nstd200human GRCh37 chr11: 44,962,333-44,962,396 , GRCh38.p12 chr11: 44,940,782-44,940,845 TP53I11
    nsv4760248insertion1nstd199human GRCh37 chr11: 44,963,574-44,963,574 , GRCh38.p12 chr11: 44,942,023-44,942,023 TP53I11
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4729649copy number variation1nstd102humanUncertain significance GRCh37 chr11: 44,266,593-46,123,796 , GRCh38.p12 chr11: 44,245,043-46,102,245 LOC105376654, PHF21A, 31 more genes
    nsv4603262copy number variation1nstd183human GRCh37 chr11: 44,920,626-45,010,015 , GRCh38.p12 chr11: 44,899,075-44,988,464 LINC02685, LOC105376649, 2 more genes
    nsv4445823insertion1nstd175human GRCh37 chr11: 44,963,574-44,963,574 , GRCh38.p12 chr11: 44,942,023-44,942,023 TP53I11
    nsv4206096copy number variation1nstd166human GRCh37.p13 chr11: 44,962,333-44,962,396 , GRCh38.p12 chr11: 44,940,782-44,940,845 TP53I11
    nsv4195652copy number variation1nstd166human GRCh37.p13 chr11: 44,963,807-44,963,949 , GRCh38.p12 chr11: 44,942,256-44,942,398 TP53I11
    nsv3944131insertion1nstd167human GRCh37 chr11: 44,963,574-44,963,574 , GRCh38.p12 chr11: 44,942,023-44,942,023 TP53I11
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