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Items: 1 to 20 of 145

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5921405copy number variation1nstd209human GRCh38 chr11: 94,508,192-94,514,054 , GRCh37.p13 chr11: 94,241,358-94,247,220 C11orf97, MRE11
    nsv5859689copy number variation1nstd209human GRCh38 chr11: 94,507,814-94,515,258 , GRCh37.p13 chr11: 94,240,980-94,248,424 MRE11, C11orf97
    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
    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
    nsv5037979inversion1nstd200human GRCh38 chr11: 93,899,952-96,855,215 , GRCh37.p13 chr11: 93,633,118-96,726,215 , GPR83, 52 more genes
    nsv4971714copy number variation1nstd200human GRCh38 chr11: 94,530,306-94,534,945 , GRCh37.p13 chr11: 94,263,472-94,268,111 C11orf97
    nsv4971591copy number variation1nstd200human GRCh38 chr11: 91,285,470-94,799,390 , GRCh37.p13 chr11: 91,018,638-94,532,556 , LOC105369429, 53 more genes
    nsv4839969copy number variation1nstd200human GRCh37 chr11: 91,018,638-94,532,556 , GRCh38.p12 chr11: 91,285,470-94,799,390 , MIR548L, 53 more genes
    nsv4729076copy number variation1nstd102humanUncertain significance GRCh37 chr11: 93,676,223-94,342,737 , GRCh38.p12 chr11: 93,943,057-94,609,571 HEPHL1, ARPC3P3, 14 more genes
    nsv4208388copy number variation1nstd166human GRCh37.p13 chr11: 94,241,398-94,247,221 , GRCh38.p12 chr11: 94,508,232-94,514,055 MRE11, C11orf97
    nsv3922508copy number variation1nstd102humanPathogenic GRCh38 chr11: 85,242,847-102,920,097 , GRCh37 chr11: 84,953,891-102,738,968 , NCBI36 chr11: 84,631,539-102,296,037 AMOTL1, LNCRNA-IUR, 240 more genes
    nsv3921121copy number variation1nstd102humanPathogenic GRCh38 chr11: 75,941,754-98,357,960 , NCBI36 chr11: 75,330,446-97,733,898 , GRCh37 chr11: 75,652,798-98,228,688 LOC105369441, RNU6-1135P, 296 more genes
    nsv3916760copy number variation1nstd102humanUncertain significance NCBI36 chr11: 93,697,096-95,454,478 , GRCh38 chr11: 94,324,282-96,081,666 , GRCh37 chr11: 94,057,448-95,814,830 SESN3, SRSF8BP, 36 more genes
    nsv3913977copy number variation1nstd102humanPathogenic GRCh37 chr11: 77,943,882-106,650,146 , GRCh38 chr11: 78,232,836-106,779,420 , NCBI36 chr11: 77,621,530-106,155,356 PLS1P1, SNORA25, 349 more genes
    nsv3910663copy number variation1nstd102humanPathogenic GRCh38 chr11: 91,086,659-109,595,582 , NCBI36 chr11: 90,459,475-108,971,518 , GRCh37 chr11: 90,819,827-109,466,308 LOC101060084, PGAM1P9, 230 more genes
    nsv3910101copy number variation1nstd102humanPathogenic NCBI36 chr11: 87,796,211-113,996,548 , GRCh37.p13 chr11: 88,156,563-114,491,338 , GRCh38.p12 chr11: 88,423,395-114,620,616 PHB1P16, LOC100418884, 385 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
    nsv3906008copy number variation1nstd102humanPathogenic GRCh37 chr11: 83,179,196-94,716,998 , GRCh38.p12 chr11: 83,468,153-94,983,834 SNORA18, PIWIL4, 157 more genes
    nsv3904761copy number variation1nstd102humanPathogenic GRCh37 chr11: 80,053,454-113,316,236 , GRCh38.p12 chr11: 80,342,410-113,445,514 RPS6P16, CTSC, 449 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
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