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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973872inversion1nstd209human GRCh38 chr6: 132,165,589-132,167,549 , GRCh37.p13 chr6: 132,486,729-132,488,689 LINC01013
    nsv5968494inversion1nstd209human GRCh38 chr6: 125,606,968-134,343,905 , GRCh37.p13 chr6: 125,928,114-134,665,043 , ARG1, 137 more genes
    nsv5906945copy number variation1nstd209human GRCh38 chr6: 123,301,756-132,349,395 , GRCh37.p13 chr6: 123,622,901-132,670,534 , LOC105377999, 105 more genes
    nsv5562129sequence alteration1nstd206human GRCh38 chr6: 132,165,590-132,167,550 , GRCh37.p13 chr6: 132,486,730-132,488,690 LINC01013
    nsv5363393translocation1nstd200human GRCh38 chr6: 132,167,166-132,167,166 , GRCh38 chr6: 132,166,142-132,166,142 , GRCh37.p13 chr6: 132,487,282-132,487,282 , GRCh37.p13 chr6: 132,488,306-132,488,306 LINC01013
    nsv5363392translocation1nstd200human GRCh38 chr6: 132,167,550-132,167,550 , GRCh38 chr6: 132,165,590-132,165,590 , GRCh37.p13 chr6: 132,486,730-132,486,730 , GRCh37.p13 chr6: 132,488,690-132,488,690 LINC01013
    nsv5341026translocation1nstd200human GRCh37 chr6: 132,488,306-132,488,306 , GRCh37 chr6: 132,487,282-132,487,282 , GRCh38.p12 chr6: 132,167,166-132,167,166 , GRCh38.p12 chr6: 132,166,142-132,166,142 LINC01013
    nsv5332685translocation1nstd200human GRCh37 chr6: 132,488,690-132,488,690 , GRCh37 chr6: 132,486,731-132,486,731 , GRCh38.p12 chr6: 132,167,550-132,167,550 , GRCh38.p12 chr6: 132,165,591-132,165,591 LINC01013
    nsv5327653translocation1nstd204human GRCh38.p13 chr6: 132,166,142-132,166,142 , GRCh38.p13 chr6: 132,167,166-132,167,166 , GRCh37.p13 chr6: 132,488,306-132,488,306 , GRCh37.p13 chr6: 132,487,282-132,487,282 LINC01013
    nsv5320951translocation1nstd204human GRCh38.p13 chr6: 132,167,550-132,167,550 , GRCh38.p13 chr6: 132,165,591-132,165,591 , GRCh37.p13 chr6: 132,486,731-132,486,731 , GRCh37.p13 chr6: 132,488,690-132,488,690 LINC01013
    nsv5168554mobile element insertion1nstd203human GRCh38 chr6: 132,152,186-132,152,209 , GRCh37.p13 chr6: 132,473,326-132,473,349 LINC01013
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4934152copy number variation1nstd200human GRCh38 chr6: 132,125,892-132,136,263 , GRCh37.p13 chr6: 132,447,032-132,457,403 LINC01013
    nsv4934148copy number variation1nstd200human GRCh38 chr6: 132,013,279-132,300,375 , GRCh37.p13 chr6: 132,334,419-132,621,514 EEF1A1P36, MOXD1, 2 more genes
    nsv4826492copy number variation1nstd200human GRCh37 chr6: 132,452,152-132,453,268 , GRCh38.p12 chr6: 132,131,012-132,132,128 LINC01013
    nsv4826491copy number variation1nstd200human GRCh37 chr6: 132,447,032-132,457,403 , GRCh38.p12 chr6: 132,125,892-132,136,263 LINC01013
    nsv4572340sequence alteration1nstd166human GRCh37.p13 chr6: 132,486,729-132,488,690 , GRCh38.p12 chr6: 132,165,589-132,167,550 LINC01013
    nsv4494099mobile element insertion1nstd166human GRCh37.p13 chr6: 132,473,326-132,473,326 , GRCh38.p12 chr6: 132,152,186-132,152,186 LINC01013
    nsv4482953mobile element insertion1nstd166human GRCh37.p13 chr6: 132,454,036-132,454,036 , GRCh38.p12 chr6: 132,132,896-132,132,896 LINC01013
    nsv4455443copy number variation1nstd102humanUncertain significance GRCh37 chr6: 131,673,206-132,706,248 , GRCh38.p12 chr6: 131,352,066-132,385,109 CTAGE9, SELENOKP2, 17 more genes
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