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Items: 1 to 20 of 91

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7071741inversion1nstd229human GRCh38 chr11: 17,252,001-17,532,480 , GRCh37.p13 chr11: 17,273,548-17,554,027 ABCC8, NUCB2, 5 more genes
    nsv7070030inversion1nstd229human GRCh38 chr11: 16,966,270-21,356,221 , GRCh37.p13 chr11: 16,987,817-21,377,767 DBX1, PRMT3, 93 more genes
    nsv7067983inversion1nstd229human GRCh38 chr11: 17,304,327-18,032,820 , GRCh37.p13 chr11: 17,325,874-18,054,367 LOC107984317, LINC02729, 12 more genes
    nsv7058428inversion1nstd229human GRCh38 chr11: 14,504,801-17,598,701 , GRCh37.p13 chr11: 14,526,347-17,620,248 RPL36AP37, LOC105376567, 41 more genes
    nsv6917151copy number variation1nstd229human GRCh38 chr11: 9,940,109-18,580,574 , GRCh37.p13 chr11: 9,961,656-18,602,121 MYOD1, MIR8070, 139 more genes
    nsv6914530copy number variation1nstd229human GRCh38 chr11: 17,382,092-17,384,501 , GRCh37.p13 chr11: 17,403,639-17,406,048 KCNJ11
    nsv6904826copy number variation1nstd229human GRCh38 chr11: 17,347,997-17,527,034 , GRCh37.p13 chr11: 17,369,544-17,548,581 NUCB2, USH1C, 5 more genes
    nsv6590311inversion1nstd223human GRCh38 chr11: 16,144,251-19,584,623 , GRCh37.p13 chr11: 16,165,797-19,606,170 LDHC, GLTPP1, 85 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
    nsv6132090copy number variation1nstd213human GRCh37 chr11: 17,410,000-17,840,001 , GRCh38.p12 chr11: 17,388,453-17,818,454 KCNC1, KCNJ11, 7 more genes
    nsv5508997copy number variation1nstd206human GRCh38 chr11: 17,382,091-17,384,500 , GRCh37.p13 chr11: 17,403,638-17,406,047 , KCNJ11
    nsv5507673copy number variation1nstd206human GRCh38 chr11: 16,359,999-20,627,000 , GRCh37.p13 chr11: 16,381,545-20,648,546 , CSRP3, 102 more genes
    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
    nsv4984228copy number variation1nstd200human GRCh38 chr11: 17,347,997-17,527,034 , GRCh37.p13 chr11: 17,369,544-17,548,581 , USH1C, 6 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
    nsv4675502copy number variation1nstd102humanPathogenic GRCh37 chr11: 13,970,757-27,565,888 , GRCh38.p12 chr11: 13,949,210-27,544,341 MRGPRX5P, LDHC, 171 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
    nsv4674824copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,053,978-34,732,891 , GRCh38.p12 chr11: 11,032,431-34,711,344 SNORA88, LINC02729, 305 more genes
    nsv4602717copy number variation1nstd183human GRCh37 chr11: 16,913,860-18,038,721 , GRCh38.p12 chr11: 16,892,313-18,017,174 , LINC02729, 27 more genes
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