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Items: 1 to 20 of 142

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5919345copy number variation1nstd209human GRCh38 chr11: 76,373,147-76,373,517 , GRCh37.p13 chr11: 76,084,191-76,084,561 THAP12
    nsv5712942mobile element insertion2nstd211human GRCh38 chr11: 76,376,762-76,376,762 , GRCh37.p13 chr11: 76,087,806-76,087,806 THAP12
    nsv5655012insertion1nstd207human GRCh38 chr11: 76,376,748-76,376,748 , GRCh37.p13 chr11: 76,087,792-76,087,792 THAP12
    nsv5499841copy number variation1nstd206human GRCh38 chr11: 76,373,139-76,373,558 , GRCh37.p13 chr11: 76,084,183-76,084,602 THAP12
    nsv5394863mobile element insertion1nstd206human GRCh38 chr11: 76,376,762-76,376,813 , GRCh37.p13 chr11: 76,087,806-76,087,857 THAP12
    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
    nsv5363222translocation1nstd200human GRCh38 chr11: 76,381,132-76,381,132 , GRCh38 chr6: 90,590,715-90,590,715 , GRCh37.p13 chr11: 76,092,176-76,092,176 , GRCh37.p13 chr6: 91,300,434-91,300,434 GVQW3, THAP12
    nsv5343069translocation1nstd200human GRCh37 chr11: 76,092,176-76,092,176 , GRCh37 chr6: 91,300,434-91,300,434 , GRCh38.p12 chr11: 76,381,132-76,381,132 , GRCh38.p12 chr6: 90,590,715-90,590,715 GVQW3, THAP12
    nsv5136761mobile element insertion1nstd203human GRCh38 chr11: 76,376,752-76,376,762 , GRCh37.p13 chr11: 76,087,796-76,087,806 THAP12
    nsv5135762mobile element insertion1nstd203human GRCh38 chr11: 76,376,748-76,376,762 , GRCh37.p13 chr11: 76,087,792-76,087,806 THAP12
    nsv4717457mobile element insertion1nstd186human GRCh37 chr11: 76,087,792-76,087,792 , GRCh38.p12 chr11: 76,376,748-76,376,748 THAP12
    nsv4671669copy number variation1nstd186human GRCh37 chr11: 76,091,921-76,091,975 , GRCh38.p12 chr11: 76,380,877-76,380,931 THAP12, GVQW3
    nsv4607500copy number variation1nstd183human GRCh37 chr11: 76,091,921-76,091,975 , GRCh38.p12 chr11: 76,380,877-76,380,931 THAP12, GVQW3
    nsv4496282mobile element insertion1nstd166human GRCh37.p13 chr11: 76,087,792-76,087,792 , GRCh38.p12 chr11: 76,376,748-76,376,748 THAP12
    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
    nsv3916301copy number variation1nstd102humanPathogenic GRCh38 chr11: 71,928,796-77,064,521 , GRCh37 chr11: 71,639,842-76,751,808 , NCBI36 chr11: 71,317,490-76,453,216 RN7SL786P, LIPT2-AS1, 146 more genes
    nsv3915804copy number variation1nstd102humanPathogenic GRCh37 chr11: 71,680,927-77,943,941 , NCBI36 chr11: 71,358,575-77,621,589 , GRCh38 chr11: 71,969,881-78,232,895 TPBGL, MAP6, 173 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
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 RTN3, KRTAP5-13P, 2833 more genes
    nsv3898361copy number variation1nstd102humanPathogenic GRCh37 chr11: 71,588,805-116,680,918 , GRCh38.p12 chr11: 71,877,759-116,810,202 SESN3, LOC107984352, 694 more genes
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