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Items: 1 to 20 of 54

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv4870911inversion1nstd200human GRCh37 chr11: 58,446,132-60,252,987 , GRCh38.p12 chr11: 58,678,659-60,485,514 LOC100422398, LOC100287485, 78 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
    nsv4607109copy number variation1nstd183human GRCh37 chr11: 59,664,384-59,714,155 , GRCh38.p12 chr11: 59,896,911-59,946,682 , GRCh38.p12 chr11|NW_019805498.1: 1-36,337 OOSP1, SRD5A3P1, 1 more genes
    nsv3920536copy number variation1nstd102humanLikely benign GRCh37 chr11: 59,618,746-60,466,753 , NCBI36 chr11: 59,375,322-60,223,329 , GRCh38 chr11: 59,851,273-60,699,280 MS4A3, MS4A2, 23 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 RTN3, KRTAP5-13P, 2833 more genes
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 LOC105376598, OSBPL9P2, 2842 more genes
    nsv3890886copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 58,935,215-62,177,656 , GRCh38.p12 chr11: 59,167,742-62,410,184 MYRF, TMEM258, 137 more genes
    nsv3168776inversion1nstd158human GRCh37 chr11: 37,074,771-61,357,521 , GRCh38.p12 chr11: 37,053,221-61,590,049 , ACP2, 535 more genes
    nsv3168425copy number variation1nstd158human GRCh37 chr11: 3,543,079-67,662,509 , GRCh38.p12 chr11: 3,521,849-67,895,038 , ACP2, 1535 more genes
    nsv1585381short tandem repeat2nstd128human GRCh37 chr11: 59,666,946-59,666,965 , GRCh38.p12 chr11: 59,899,473-59,899,492 OOSP3, SRD5A3P1
    nsv1585380short tandem repeat2nstd128human GRCh37 chr11: 59,665,537-59,665,549 , GRCh38.p12 chr11: 59,898,064-59,898,076 SRD5A3P1, OOSP3
    nsv1146381inversion1nstd107human GRCh37 chr11: 1,620,499-71,272,308 , GRCh38.p12 chr11: 1,599,269-71,561,262 , ACP2, 1686 more genes
    nsv1132999inversion1nstd106human GRCh37 chr11: 1,620,508-89,079,908 , GRCh38.p12 chr11: 1,599,278-89,346,740 , ACTN3, 2007 more genes
    nsv1125301inversion1nstd106human GRCh37 chr11: 48,489,096-88,979,496 , GRCh38.p12 chr11: 48,467,544-89,246,328 , MRPL49, 1130 more genes
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