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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077950inversion1nstd229human GRCh38 chr11: 6,003,081-6,030,570 , GRCh37.p13 chr11: 6,024,311-6,051,800 RNA5SP329, OR56A4, 2 more genes
    nsv6918063copy number variation1nstd229human GRCh38 chr11: 6,002,366-6,002,584 , GRCh37.p13 chr11: 6,023,596-6,023,814 OR56A4, LOC107984303
    nsv6917011copy number variation1nstd229human GRCh38 chr11: 2,693,282-9,207,515 , GRCh37.p13 chr11: 2,714,512-9,229,062 LOC105376526, OR51E2, 279 more genes
    nsv6904581copy number variation1nstd229human GRCh38 chr11: 5,990,529-6,000,587 , GRCh37.p13 chr11: 6,011,759-6,021,817 KRT18P58, OR56A4
    nsv6902882copy number variation1nstd229human GRCh38 chr11: 5,999,771-5,999,893 , GRCh37.p13 chr11: 6,021,001-6,021,123 OR56A4
    nsv6637864copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177 PNPLA2, OR52H1, 372 more genes
    nsv6621193copy number variation1nstd224human GRCh37 chr11: 6,024,349-6,048,372 , GRCh38.p12 chr11: 6,003,119-6,027,142 LOC107984303, OR56A1, 2 more genes
    nsv6621123copy number variation1nstd224human GRCh37 chr11: 5,966,415-6,090,372 , GRCh38.p12 chr11: 5,945,185-6,069,142 OR52L2P, OR52L1, 9 more genes
    nsv6591496inversion1nstd223human GRCh38 chr11: 6,003,072-6,030,573 , GRCh37.p13 chr11: 6,024,302-6,051,803 OR56A4, OR56A1, 2 more genes
    nsv6441849copy number variation1nstd223human GRCh38 chr11: 5,588,812-6,011,442 , GRCh37.p13 chr11: 5,610,042-6,032,672 OR52N5, OR52N4, 26 more genes
    nsv6437487copy number variation1nstd223human GRCh38 chr11: 5,568,264-6,075,481 , GRCh37.p13 chr11: 5,589,494-6,096,711 TRIM34, OR52E6, 33 more genes
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv5373407translocation1nstd200human GRCh38 chr11: 6,003,073-6,003,073 , GRCh38 chr11: 6,033,633-6,033,633 , GRCh37.p13 chr11: 6,024,303-6,024,303 , GRCh37.p13 chr11: 6,054,863-6,054,863 LOC107984303, OR56A4
    nsv4768373copy number variation1nstd102humanPathogenic GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811 LOC107984302, STK33, 375 more genes
    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
    nsv4681173copy number variation2nstd102humanUncertain significance GRCh37 chr11: 5,709,028-6,640,651 , GRCh38.p12 chr11: 5,687,798-6,619,420 OR56B2P, TRIM3, 50 more genes
    nsv4675693copy number variation1nstd102humanLikely benign GRCh37 chr11: 5,505,304-6,199,376 , GRCh38.p12 chr11: 5,484,074-6,178,146 OR52B5P, HNRNPA1P53, 47 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4603739copy number variation2nstd183human GRCh37 chr11: 6,005,905-6,159,840 , GRCh38.p12 chr11: 5,984,675-6,138,610 OR56A4, OR56A1, 9 more genes
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