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Items: 1 to 20 of 78

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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
    nsv5325627inversion1nstd204human GRCh37.p13 chr11: 58,669,453-61,321,541 , GRCh38.p13 chr11: 58,901,980-61,554,069 , CD5, 118 more genes
    nsv4984990copy number variation1nstd200human GRCh38 chr11: 60,931,698-60,971,997 , GRCh37.p13 chr11: 60,699,170-60,739,469 SLC15A3, CD6, 1 more genes
    nsv4885672inversion1nstd200human GRCh37 chr11: 58,669,461-61,321,541 , GRCh38.p12 chr11: 58,901,988-61,554,069 , MS4A2, 118 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
    nsv4675148copy number variation1nstd102humanUncertain significance GRCh37 chr11: 60,385,382-62,456,278 , GRCh38.p12 chr11: 60,617,909-62,688,806 LOC105369326, MS4A18, 91 more genes
    nsv4457060copy number variation1nstd102humanUncertain significance GRCh37 chr11: 60,499,486-61,529,578 , GRCh38.p12 chr11: 60,732,013-61,762,106 TMEM109, LOC101927495, 41 more genes
    nsv4204410copy number variation1nstd166human GRCh37.p13 chr11: 60,696,559-60,697,379 , GRCh38.p12 chr11: 60,929,087-60,929,907 TMEM132A
    nsv4193562copy number variation1nstd166human GRCh37.p13 chr11: 60,694,241-60,695,196 , GRCh38.p12 chr11: 60,926,769-60,927,724 TMEM132A
    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
    nsv3891516copy number variation1nstd102humanBenign GRCh37 chr11: 60,690,580-60,708,611 , GRCh38.p12 chr11: 60,923,108-60,941,139 TMEM109, SLC15A3, 1 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
    nsv3143591copy number variation1nstd151human GRCh37 chr11: 60,150,612-60,714,298 , GRCh38.p12 chr11: 60,383,139-60,946,826 , MS4A19P, 22 more genes
    nsv3142736copy number variation1nstd151human GRCh37 chr11: 60,107,336-60,714,298 , GRCh38.p12 chr11: 60,339,863-60,946,826 , MS4A15, 23 more genes
    nsv3139979copy number variation1nstd151human GRCh37 chr11: 60,687,163-60,714,298 , GRCh38.p12 chr11: 60,919,691-60,946,826 TMEM109, SLC15A3, 1 more genes
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