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Items: 1 to 20 of 129

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5850595copy number variation1nstd209human GRCh38 chr11: 96,335,501-96,353,194 , GRCh37.p13 chr11: 96,068,665-96,086,358 CCDC82, MAML2, 1 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
    nsv5498179copy number variation1nstd206human GRCh38 chr11: 96,370,217-96,370,336 , GRCh37.p13 chr11: 96,103,381-96,103,500 CCDC82
    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
    nsv4989189copy number variation1nstd200human GRCh38 chr11: 96,253,825-96,817,793 , GRCh37.p13 chr11: 95,986,989-96,688,793 MIR1260B, RNA5SP346, 6 more genes
    nsv4971775copy number variation1nstd200human GRCh38 chr11: 96,385,463-96,387,207 , GRCh37.p13 chr11: 96,118,627-96,120,371 CCDC82
    nsv4971774copy number variation1nstd200human GRCh38 chr11: 96,350,572-96,350,861 , GRCh37.p13 chr11: 96,083,736-96,084,025 CCDC82
    nsv4845111copy number variation1nstd200human GRCh37 chr11: 96,118,627-96,120,371 , GRCh38.p12 chr11: 96,385,463-96,387,207 CCDC82
    nsv4728836copy number variation1nstd102humanUncertain significance GRCh37 chr11: 95,822,513-97,875,558 , GRCh38.p12 chr11: 96,089,349-98,004,830 CCDC82, RNA5SP347, 14 more genes
    nsv4675744copy number variation1nstd102humanUncertain significance GRCh37 chr11: 95,841,847-96,810,072 , GRCh38.p12 chr11: 96,108,683-96,939,072 CCDC82, JRKL-AS1, 6 more genes
    nsv4675242copy number variation1nstd102humanUncertain significance GRCh37 chr11: 95,878,455-98,553,076 , GRCh38.p12 chr11: 96,145,291-98,682,346 LOC100289416, LOC105369453, 17 more genes
    nsv4510417mobile element insertion1nstd166human GRCh37.p13 chr11: 96,085,887-96,085,887 , GRCh38.p12 chr11: 96,352,723-96,352,723 CCDC82
    nsv4504030mobile element insertion1nstd166human GRCh37.p13 chr11: 96,101,454-96,101,454 , GRCh38.p12 chr11: 96,368,290-96,368,290 CCDC82
    nsv4499004mobile element insertion1nstd166human GRCh37.p13 chr11: 96,115,997-96,115,997 , GRCh38.p12 chr11: 96,382,833-96,382,833 CCDC82
    nsv4209047copy number variation1nstd166human GRCh37.p13 chr11: 96,103,381-96,103,500 , GRCh38.p12 chr11: 96,370,217-96,370,336 CCDC82
    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
    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
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