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Items: 1 to 20 of 222

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5687343mobile element insertion1nstd211human GRCh38 chr5: 87,377,896-87,377,896 , GRCh37.p13 chr5: 86,673,713-86,673,713 RASA1, CCNH
    nsv5469062copy number variation1nstd206human GRCh38 chr5: 87,313,159-87,321,244 , GRCh37.p13 chr5: 86,608,976-86,617,061 LOC644285, CCNH, 1 more genes
    nsv5457938copy number variation1nstd206human GRCh38 chr5: 87,349,389-87,349,496 , GRCh37.p13 chr5: 86,645,206-86,645,313 CCNH, RASA1
    nsv5406968mobile element insertion1nstd206human GRCh38 chr5: 87,377,896-87,377,947 , GRCh37.p13 chr5: 86,673,713-86,673,764 CCNH, RASA1
    nsv5337441translocation1nstd200human GRCh37 chr5: 86,703,521-86,703,521 , GRCh37 chr5: 86,707,680-86,707,680 , GRCh38.p12 chr5: 87,411,863-87,411,863 , GRCh38.p12 chr5: 87,407,704-87,407,704 LOC105379066, CCNH
    nsv5334579translocation1nstd200human GRCh37 chr5: 86,701,163-86,701,163 , GRCh37 chr5: 86,708,121-86,708,121 , GRCh38.p12 chr5: 87,412,304-87,412,304 , GRCh38.p12 chr5: 87,405,346-87,405,346 CCNH, LOC105379066
    nsv5236975copy number variation1nstd204human GRCh38.p13 chr5: 87,359,221-87,360,420 , GRCh37.p13 chr5: 86,655,038-86,656,237 RASA1, CCNH
    nsv5160580mobile element insertion1nstd203human GRCh38 chr5: 87,372,560-87,372,568 , GRCh37.p13 chr5: 86,668,377-86,668,385 RASA1, CCNH
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5033775inversion1nstd200human GRCh38 chr5: 76,373,686-102,541,075 , GRCh37.p13 chr5: 75,669,511-101,876,779 , F2RL1, 331 more genes
    nsv4947057copy number variation1nstd200human GRCh38 chr5: 87,323,934-87,327,349 , GRCh37.p13 chr5: 86,619,751-86,623,166 LOC644285, RASA1, 1 more genes
    nsv4947056copy number variation1nstd200human GRCh38 chr5: 87,314,204-87,315,471 , GRCh37.p13 chr5: 86,610,021-86,611,288 CCNH, RASA1
    nsv4947055copy number variation1nstd200human GRCh38 chr5: 87,309,793-87,313,736 , GRCh37.p13 chr5: 86,605,610-86,609,553 RASA1, CCNH
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4793216copy number variation1nstd200human GRCh37 chr5: 86,619,751-86,623,166 , GRCh38.p12 chr5: 87,323,934-87,327,349 CCNH, LOC644285, 1 more genes
    nsv4793215copy number variation1nstd200human GRCh37 chr5: 86,605,610-86,609,553 , GRCh38.p12 chr5: 87,309,793-87,313,736 CCNH, RASA1
    nsv4675667copy number variation1nstd102humanPathogenic GRCh37 chr5: 72,790,061-97,478,870 , GRCh38.p12 chr5: 73,494,236-98,143,166 LOC101929380, LIX1-AS1, 318 more genes
    nsv4598316copy number variation1nstd183human GRCh37 chr5: 86,628,839-86,633,974 , GRCh38.p12 chr5: 87,333,022-87,338,157 RASA1, CCNH
    nsv4560903mobile element insertion1nstd166human GRCh37.p13 chr5: 86,639,114-86,639,114 , GRCh38.p12 chr5: 87,343,297-87,343,297 RASA1, CCNH
    nsv4559343mobile element insertion1nstd166human GRCh37.p13 chr5: 86,668,377-86,668,377 , GRCh38.p12 chr5: 87,372,560-87,372,560 RASA1, CCNH
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