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Items: 1 to 20 of 127

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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
    nsv6909127copy number variation1nstd229human GRCh38 chr11: 64,917,822-64,924,482 , GRCh37.p13 chr11: 64,685,294-64,691,954 PPP2R5B
    nsv6905877copy number variation1nstd229human GRCh38 chr11: 60,405,001-68,536,600 , GRCh37.p13 chr11: 60,172,474-68,304,068 INCENP, SNRPCP12, 409 more genes
    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
    nsv6902983copy number variation1nstd229human GRCh38 chr11: 64,925,085-64,925,219 , GRCh37.p13 chr11: 64,692,557-64,692,691 PPP2R5B
    nsv6901653copy number variation1nstd229human GRCh38 chr11: 64,916,538-64,920,431 , GRCh37.p13 chr11: 64,684,010-64,687,903 ATG2A, PPP2R5B
    nsv6467972copy number variation1nstd223human GRCh38 chr11: 64,845,523-64,919,247 , GRCh37.p13 chr11: 64,612,995-64,686,719 RPS16P6, MIR194-2, 8 more genes
    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
    nsv6309121copy number variation2nstd102humanPathogenic GRCh37 chr11: 64,522,783-66,283,694 , GRCh38.p12 chr11: 64,755,311-66,516,223 SF3B2, ZNRD2-DT, 124 more genes
    nsv6132269copy number variation1nstd213human GRCh37 chr11: 64,390,000-65,950,001 , GRCh38.p12 chr11: 64,622,528-66,182,530 MRPL49, CTSW, 103 more genes
    nsv6132112copy number variation1nstd213human GRCh37 chr11: 64,220,000-68,010,001 , GRCh38.p12 chr11: 64,452,528-68,242,533 ACTN3, ALDH3B1, 212 more genes
    nsv5497530copy number variation1nstd206human GRCh38 chr11: 64,925,085-64,925,219 , GRCh37.p13 chr11: 64,692,557-64,692,691 PPP2R5B
    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
    nsv5267852copy number variation1nstd204human GRCh38.p13 chr11: 64,173,401-65,676,300 , GRCh37.p13 chr11: 63,940,873-65,443,771 , TALAM1, 103 more genes
    nsv4985045copy number variation1nstd200human GRCh38 chr11: 64,845,523-64,919,251 , GRCh37.p13 chr11: 64,612,995-64,686,723 MIR6750, ATG2A, 8 more genes
    nsv4979813copy number variation1nstd200human GRCh38 chr11: 64,920,009-64,924,109 , GRCh37.p13 chr11: 64,687,481-64,691,581 PPP2R5B
    nsv4843432copy number variation1nstd200human GRCh37 chr11: 64,687,481-64,691,581 , GRCh38.p12 chr11: 64,920,009-64,924,109 PPP2R5B
    nsv4837136copy number variation1nstd200human GRCh37 chr11: 64,695,687-64,705,996 , GRCh38.p12 chr11: 64,928,215-64,938,524 MAJIN, GPHA2, 1 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
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