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Items: 1 to 20 of 110

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093694copy number variation2nstd102humanUncertain significance GRCh37 chr11: 58,916,346-64,972,349 , GRCh38.p12 chr11: 59,148,873-65,204,878 VPS37C, POLR2G, 298 more genes
    nsv7076174inversion1nstd229human GRCh38 chr11: 57,437,573-64,138,990 , GRCh37.p13 chr11: 57,205,046-63,906,462 RNU2-2P, SLC43A1, 299 more genes
    nsv7066241inversion1nstd229human GRCh38 chr11: 60,058,237-60,062,962 , GRCh37.p13 chr11: 59,825,710-59,830,435 MS4A3
    nsv6917257copy number variation1nstd229human GRCh38 chr11: 60,055,033-60,108,713 , GRCh37.p13 chr11: 59,822,506-59,876,186 MS4A3, MS4A2, 1 more genes
    nsv6909750copy number variation1nstd229human GRCh38 chr11: 60,060,976-60,066,044 , GRCh37.p13 chr11: 59,828,449-59,833,517 MS4A3
    nsv6904436copy number variation1nstd229human GRCh38 chr11: 60,062,701-60,077,300 , GRCh37.p13 chr11: 59,830,174-59,844,773 MS4A3, YWHAZP9
    nsv6903095copy number variation1nstd229human GRCh38 chr11: 59,466,654-66,168,743 , GRCh37.p13 chr11: 59,234,127-65,936,214 LINC02724, TMEM132A, 342 more genes
    nsv6621192copy number variation1nstd224human GRCh37 chr11: 59,826,857-59,949,106 , GRCh38.p12 chr11: 60,059,384-60,181,633 MS4A3, LINC02705, 3 more genes
    nsv6579515inversion1nstd223human GRCh38 chr11: 60,067,849-60,068,548 , GRCh37.p13 chr11: 59,835,322-59,836,021 MS4A3
    nsv6577262inversion1nstd223human GRCh38 chr11: 60,067,752-60,068,447 , GRCh37.p13 chr11: 59,835,225-59,835,920 MS4A3
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6315474copy number variation1nstd102humanPathogenic GRCh37 chr11: 43,607,886-61,466,671 , GRCh38.p12 chr11: 43,586,336-61,699,199 TRR-TCT3-2, OR4A41P, 494 more genes
    nsv5922900copy number variation1nstd209human GRCh38 chr11: 60,067,824-60,067,962 , GRCh37.p13 chr11: 59,835,297-59,835,435 MS4A3
    nsv5921314copy number variation1nstd209human GRCh38 chr11: 60,059,601-60,059,653 , GRCh37.p13 chr11: 59,827,074-59,827,126 MS4A3
    nsv5908038copy number variation1nstd209human GRCh37.p13 chr11: 59,811,970-59,993,085 , GRCh38 chr11: 60,044,497-60,225,612 MS4A3, MS4A2, 6 more genes
    nsv5858743copy number variation1nstd209human GRCh38 chr11: 60,044,479-60,056,509 , GRCh37.p13 chr11: 59,811,952-59,823,982 MS4A3, OOSP2
    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
    nsv5326104inversion1nstd204human GRCh37.p13 chr11: 58,446,123-60,252,987 , GRCh38.p13 chr11: 58,678,650-60,485,514 OSBP, OR5BB1P, 78 more genes
    nsv5325627inversion1nstd204human GRCh37.p13 chr11: 58,669,453-61,321,541 , GRCh38.p13 chr11: 58,901,980-61,554,069 , CD5, 118 more genes
    nsv4885672inversion1nstd200human GRCh37 chr11: 58,669,461-61,321,541 , GRCh38.p12 chr11: 58,901,988-61,554,069 , MS4A2, 118 more genes
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