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Items: 1 to 20 of 190

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093840copy number variation1nstd102humanUncertain significance GRCh37 chr11: 18,301,429-18,428,828 , GRCh38.p12 chr11: 18,279,882-18,407,281 LDHA, MIR3159, 3 more genes
    nsv7070173inversion1nstd229human GRCh38 chr11: 18,169,244-18,915,403 , GRCh37.p13 chr11: 18,190,791-18,936,950 TSG101, MIR3159, 33 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
    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
    nsv6916107copy number variation1nstd229human GRCh38 chr11: 18,276,205-18,286,501 , GRCh37.p13 chr11: 18,297,752-18,308,048 HPS5
    nsv6907432copy number variation1nstd229human GRCh38 chr11: 18,313,633-18,315,379 , GRCh37.p13 chr11: 18,335,180-18,336,926 HPS5
    nsv6903814copy number variation1nstd229human GRCh38 chr11: 18,312,263-18,312,577 , GRCh37.p13 chr11: 18,333,810-18,334,124 HPS5
    nsv6637654copy number variation1nstd102humanUncertain significance GRCh37 chr11: 17,784,556-18,797,650 , GRCh38.p12 chr11: 17,763,009-18,776,103 LOC112268073, SAAL1, 37 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
    nsv6589612inversion1nstd223human GRCh38 chr11: 18,303,634-18,304,374 , GRCh37.p13 chr11: 18,325,181-18,325,921 HPS5
    nsv6578664inversion1nstd223human GRCh38 chr11: 18,317,020-18,317,447 , GRCh37.p13 chr11: 18,338,567-18,338,994 HPS5
    nsv6452600copy number variation1nstd223human GRCh38 chr11: 18,276,205-18,286,498 , GRCh37.p13 chr11: 18,297,752-18,308,045 HPS5
    nsv6450339copy number variation1nstd223human GRCh38 chr11: 18,251,319-18,277,032 , GRCh37.p13 chr11: 18,272,866-18,298,579 ST13P5, RNA5SP334, 2 more genes
    nsv6447549copy number variation1nstd223human GRCh38 chr11: 18,313,597-18,315,424 , GRCh37.p13 chr11: 18,335,144-18,336,971 HPS5
    nsv6439747copy number variation1nstd223human GRCh38 chr11: 18,282,231-18,289,396 , GRCh37.p13 chr11: 18,303,778-18,310,943 HPS5
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6315231copy number variation1nstd102humanUncertain significance GRCh37 chr11: 18,300,216-18,308,137 , GRCh38.p12 chr11: 18,278,669-18,286,590 HPS5
    nsv6308968copy number variation1nstd102humanUncertain significance GRCh37 chr11: 18,301,429-18,307,026 , GRCh38.p12 chr11: 18,279,882-18,285,479 HPS5
    nsv6132091copy number variation1nstd213human GRCh37 chr11: 17,970,000-18,540,001 , GRCh38.p12 chr11: 17,948,453-18,518,454 GTF2H1, LDHA, 25 more genes
    nsv5976306inversion1nstd209human GRCh37.p13 chr11: 18,289,785-18,311,434 , GRCh38 chr11: 18,268,238-18,289,887 SAA1, HPS5
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