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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5918104copy number variation1nstd209human GRCh38 chr11: 104,190,618-110,044,159 , GRCh37.p13 chr11: 104,061,346-109,914,884 , CARD18, 71 more genes
    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
    nsv5509421copy number variation1nstd206human GRCh38 chr11: 105,024,553-105,024,646 , GRCh37.p13 chr11: 104,895,280-104,895,373 CASP1
    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
    nsv5260743copy number variation1nstd204human GRCh38.p13 chr11: 105,034,254-105,044,377 , GRCh37.p13 chr11: 104,904,981-104,915,104 CASP1, CARD16
    nsv4989250copy number variation1nstd200human GRCh38 chr11: 104,163,006-105,424,224 , GRCh37.p13 chr11: 104,033,734-105,294,951 LOC105369468, CASP1P1, 19 more genes
    nsv4709877copy number variation1nstd195human GRCh37 chr11: 104,893,001-105,284,101 , GRCh38.p12 chr11: 105,022,274-105,413,374 CASP1, CARD18, 10 more genes
    nsv4680641copy number variation1nstd189human GRCh37.p13 chr11: 104,027,037-105,291,719 , GRCh38.p12 chr11: 104,156,309-105,420,992 CASP1, CASP4, 19 more genes
    nsv4680518copy number variation1nstd189human GRCh37.p13 chr11: 104,037,015-105,276,482 , GRCh38.p12 chr11: 104,166,287-105,405,755 CASP1, CASP4, 18 more genes
    nsv4680081copy number variation1nstd189human GRCh37.p13 chr11: 104,023,678-105,291,719 , GRCh38.p12 chr11: 104,152,950-105,420,992 CASP1, CASP4, 19 more genes
    nsv4676052copy number variation1nstd102humanUncertain significance GRCh37 chr11: 103,980,525-106,914,369 , GRCh38.p12 chr11: 104,109,797-107,043,643 CARD17P, LOC643855, 36 more genes
    nsv4675822copy number variation1nstd102humanLikely benign GRCh37 chr11: 104,805,250-105,062,846 , GRCh38.p12 chr11: 104,934,523-105,192,119 LOC107984381, CARD17P, 10 more genes
    nsv4675680copy number variation1nstd102humanPathogenic GRCh37 chr11: 103,320,065-114,349,787 , GRCh38.p12 chr11: 103,449,337-114,479,065 DRD2, NCAM1, 181 more genes
    nsv4675315copy number variation1nstd102humanLikely benign GRCh37 chr11: 104,032,889-105,292,804 , GRCh38.p12 chr11: 104,162,161-105,422,077 CASP1P3, RNA5SP348, 19 more genes
    nsv4675055copy number variation1nstd102humanUncertain significance GRCh37 chr11: 103,983,847-106,914,369 , GRCh38.p12 chr11: 104,113,119-107,043,643 LOC105369466, CASP4LP, 36 more genes
    nsv4599439copy number variation1nstd183human GRCh37 chr11: 104,797,787-104,912,458 , GRCh38.p12 chr11: 104,927,060-105,041,731 CASP1, CASP5, 2 more genes
    nsv4456352copy number variation1nstd102humanUncertain significance GRCh37 chr11: 104,032,613-105,293,148 , GRCh38.p12 chr11: 104,161,885-105,422,421 CASP12, CASP4, 19 more genes
    nsv4455554copy number variation1nstd102humanPathogenic GRCh37 chr11: 104,101,411-116,680,918 , GRCh38.p12 chr11: 104,230,683-116,810,202 LINC02732, LINC02698, 198 more genes
    nsv3924464copy number variation1nstd102humanPathogenic NCBI36 chr11: 97,733,839-105,435,083 , GRCh38 chr11: 98,357,901-106,059,146 , GRCh37 chr11: 98,228,629-105,929,873 ARHGAP42, PDGFDDN, 91 more genes
    nsv3922253copy number variation1nstd102humanPathogenic GRCh37 chr11: 100,219,331-134,910,140 , NCBI36 chr11: 99,724,541-134,415,350 , GRCh38 chr11: 100,348,599-135,040,246 RPS27P19, UBASH3B, 655 more genes
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