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Items: 1 to 20 of 114

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093820copy number variation1nstd102humanUncertain significance GRCh37 chr11: 101,374,735-103,349,981 , GRCh38.p12 chr11: 101,504,004-103,479,253 WTAPP1, TMEM123, 40 more genes
    nsv7068895inversion1nstd229human GRCh38 chr11: 100,518,680-109,308,656 , GRCh37.p13 chr11: 100,389,411-109,179,383 LINC02719, RNA5SP349, 121 more genes
    nsv7064729inversion1nstd229human GRCh38 chr11: 102,706,869-103,032,485 , GRCh37.p13 chr11: 102,577,600-102,903,214 CSNK1A1P2, WTAPP1, 9 more genes
    nsv7061741inversion1nstd229human GRCh38 chr11: 100,793,881-105,425,000 , GRCh37.p13 chr11: 100,664,612-105,295,727 MTND1P36, LOC102723862, 75 more genes
    nsv6898625copy number variation1nstd229human GRCh38 chr11: 102,763,424-102,770,985 , GRCh37.p13 chr11: 102,634,155-102,641,716 LOC100421658, MMP10
    nsv6898519copy number variation1nstd229human GRCh38 chr11: 101,614,768-102,883,244 , GRCh37.p13 chr11: 101,485,499-102,702,496 PLS1P1, MMP3, 26 more genes
    nsv6637687copy number variation1nstd102humanPathogenic GRCh37 chr11: 101,371,503-109,306,519 , GRCh38.p12 chr11: 101,500,772-109,435,793 GRIA4, MTND1P36, 111 more genes
    nsv6637671copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 98,770,072-104,602,846 , GRCh38.p12 chr11: 98,899,342-104,732,118 BIRC2, BIRC3, 67 more genes
    nsv6637396copy number variation1nstd102humanPathogenic GRCh37 chr11: 81,478,509-104,667,040 , GRCh38.p12 chr11: 81,767,467-104,796,313 LOC107984375, RN7SL222P, 295 more genes
    nsv6637174copy number variation1nstd102humanUncertain significance GRCh37 chr11: 99,059,204-103,281,943 , GRCh38.p12 chr11: 99,188,473-103,411,215 TMEM123, LOC100418997, 55 more genes
    nsv6582485inversion1nstd223human GRCh38 chr11: 100,023,537-103,679,304 , GRCh37.p13 chr11: 99,894,269-103,550,032 BOLA3P1, LOC100190922, 56 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
    nsv6313981copy number variation1nstd102humanUncertain significance GRCh37 chr11: 102,308,740-102,676,879 , GRCh38.p12 chr11: 102,438,009-102,806,148 MMP1, MMP20, 11 more genes
    nsv6309019copy number variation2nstd102humanPathogenic GRCh37 chr11: 101,323,686-103,349,981 , GRCh38.p12 chr11: 101,452,955-103,479,253 RPL21P96, RNU6-952P, 40 more genes
    nsv6290834copy number variation1nstd102humanUncertain significance GRCh37 chr11: 85,422,071-118,022,671 , GRCh38.p12 chr11: 85,711,028-118,151,956 CARD17P, RNA5SP350, 480 more genes
    nsv6132066copy number variation1nstd213human GRCh37 chr11: 101,180,000-103,180,001 , GRCh38.p12 chr11: 101,309,269-103,309,272 BIRC2, MMP3, 35 more genes
    nsv6131906copy number variation1nstd213human GRCh37 chr11: 102,640,000-102,710,001 , GRCh38.p12 chr11: 102,769,269-102,839,270 MMP1, MMP3, 3 more genes
    nsv5706468mobile element insertion2nstd211human GRCh38 chr11: 102,778,257-102,778,257 , GRCh37.p13 chr11: 102,648,988-102,648,988 MMP10
    nsv5672640copy number variation1nstd102humanPathogenic GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976 HSPD1P13, CARD17P, 239 more genes
    nsv5410701mobile element insertion1nstd206human GRCh38 chr11: 102,778,257-102,778,302 , GRCh37.p13 chr11: 102,648,988-102,649,033 MMP10
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