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Items: 1 to 20 of 123

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5975420inversion1nstd209human GRCh38 chr4: 44,594,542-44,748,679 , GRCh37.p13 chr4: 44,596,559-44,750,696 GUF1, GNPDA2, 2 more genes
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 more genes
    nsv4928622copy number variation1nstd200human GRCh38 chr4: 44,687,613-44,687,754 , GRCh37.p13 chr4: 44,689,630-44,689,771 GUF1
    nsv4928618copy number variation1nstd200human GRCh38 chr4: 44,656,476-44,688,293 , GRCh37.p13 chr4: 44,658,493-44,690,310 YIPF7, GUF1
    nsv4791655copy number variation1nstd200human GRCh37 chr4: 44,689,630-44,689,771 , GRCh38.p12 chr4: 44,687,613-44,687,754 GUF1
    nsv4791614copy number variation1nstd200human GRCh37 chr4: 43,358,175-53,119,711 , GRCh38.p12 chr4: 43,356,158-52,253,545 , LOC107986277, 78 more genes
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 more genes
    nsv4753570inversion1nstd199human GRCh37 chr4: 19,034-191,028,414 , GRCh38.p12 chr4: 19,034-190,107,259 , ADD1, 2434 more genes
    nsv4751554inversion1nstd199human GRCh37 chr4: 18,939-191,034,785 , GRCh38.p12 chr4: 18,939-190,113,630 , ADD1, 2434 more genes
    nsv4714416copy number variation1nstd195human GRCh37 chr4: 44,606,301-44,746,051 , GRCh38.p12 chr4: 44,604,284-44,744,034 GUF1, GNPDA2, 2 more genes
    nsv4684161copy number variation1nstd102humanPathogenic GRCh37 chr4: 49,450-49,620,898 , GRCh38.p12 chr4: 49,556-49,618,881 TLR10, WDR1, 669 more genes
    nsv4674539copy number variation1nstd102humanUncertain significance GRCh37 chr4: 42,626,603-45,438,191 , GRCh38.p12 chr4: 42,624,586-45,436,174 GNPDA2, ATP8A1, 27 more genes
    nsv4674128copy number variation1nstd102humanLikely benign GRCh37 chr4: 44,669,198-44,770,906 , GRCh38.p12 chr4: 44,667,181-44,768,889 LOC112268465, LOC105374439, 2 more genes
    nsv4588687copy number variation1nstd183human GRCh37 chr4: 44,543,808-44,976,135 , GRCh38.p12 chr4: 44,541,791-44,974,118 GUF1, GNPDA2, 7 more genes
    nsv4475536mobile element insertion1nstd166human GRCh37.p13 chr4: 44,693,287-44,693,287 , GRCh38.p12 chr4: 44,691,270-44,691,270 GUF1
    nsv4110217copy number variation1nstd166human GRCh37.p13 chr4: 43,471,198-45,044,741 , GRCh38.p12 chr4: 43,469,181-45,042,724 GUF1, NDUFB4P12, 17 more genes
    nsv4096041copy number variation1nstd166human GRCh37.p13 chr4: 44,689,630-44,689,771 , GRCh38.p12 chr4: 44,687,613-44,687,754 GUF1
    nsv3923949copy number variation1nstd102humanPathogenic GRCh37 chr4: 40,498,493-49,581,867 , NCBI36 chr4: 40,193,250-49,276,624 , GRCh38 chr4: 40,496,476-49,579,850 CWH43, LOC100419154, 104 more genes
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