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Items: 1 to 20 of 448

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147175copy number variation1nstd232human GRCh37.p13 chr4: 184,632,824-184,632,913 , GRCh38.p12 chr4: 183,711,671-183,711,760 TRAPPC11
    nsv7096991copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr4: 184,585,021-184,585,244 , GRCh38.p12 chr4: 183,663,868-183,664,091 TRAPPC11
    nsv7096990copy number variation1nstd102humanPathogenic GRCh37 chr4: 183,245,174-184,633,797 , GRCh38.p12 chr4: 182,324,021-183,712,644 RNU6-335P, LOC101929996, 29 more genes
    nsv7093619copy number variation1nstd228human GRCh37 chr4: 171,508,974-190,957,473 , GRCh38.p12 chr4: 170,587,823-190,036,318 AGA, SLC25A4, 240 more genes
    nsv7056086inversion1nstd229human GRCh38 chr4: 174,912,619-184,252,538 , GRCh37.p13 chr4: 175,833,770-185,173,691 WDR17, LOC105377580, 84 more genes
    nsv7055054inversion1nstd229human GRCh38 chr4: 177,546,174-183,679,474 , GRCh37.p13 chr4: 178,467,328-184,600,627 RNU6-479P, VTI1BP2, 52 more genes
    nsv7054725inversion1nstd229human GRCh38 chr4: 178,850,585-188,333,056 , GRCh37.p13 chr4: 179,771,739-189,254,210 RPL6P16, LOC105377568, 125 more genes
    nsv7050592inversion1nstd229human GRCh38 chr4: 181,219,378-183,892,493 , GRCh37.p13 chr4: 182,140,531-184,813,646 ING2, VTI1BP2, 40 more genes
    nsv7048281inversion1nstd229human GRCh38 chr4: 177,590,230-186,282,308 , GRCh37.p13 chr4: 178,511,384-187,203,462 STOX2, LINC01098, 105 more genes
    nsv7038446inversion1nstd229human GRCh38 chr4: 182,834,579-184,176,114 , GRCh37.p13 chr4: 183,755,732-185,097,267 LOC105377581, FBLP1, 30 more genes
    nsv6757046copy number variation1nstd229human GRCh38 chr4: 183,711,671-183,711,761 , GRCh37.p13 chr4: 184,632,824-184,632,914 TRAPPC11
    nsv6756144copy number variation1nstd229human GRCh38 chr4: 183,509,739-183,794,572 , GRCh37.p13 chr4: 184,430,892-184,715,725 ING2, LOC105377581, 8 more genes
    nsv6755835copy number variation1nstd229human GRCh38 chr4: 183,660,997-183,663,481 , GRCh37.p13 chr4: 184,582,150-184,584,634 TRAPPC11
    nsv6752691copy number variation1nstd229human GRCh38 chr4: 183,673,476-183,677,743 , GRCh37.p13 chr4: 184,594,629-184,598,896 RNU6-335P, TRAPPC11
    nsv6751637copy number variation1nstd229human GRCh38 chr4: 183,708,801-184,045,600 , GRCh37.p13 chr4: 184,629,954-184,966,753 LOC107986330, STOX2, 2 more genes
    nsv6751409copy number variation1nstd229human GRCh38 chr4: 183,679,422-183,883,700 , GRCh37.p13 chr4: 184,600,575-184,804,853 RNU6-1053P, STOX2, 2 more genes
    nsv6750088copy number variation1nstd229human GRCh38 chr4: 183,658,839-183,663,129 , GRCh37.p13 chr4: 184,579,992-184,584,282 RWDD4, TRAPPC11
    nsv6748972copy number variation1nstd229human GRCh38 chr4: 183,673,477-183,682,943 , GRCh37.p13 chr4: 184,594,630-184,604,096 RNU6-335P, TRAPPC11
    nsv6746118copy number variation1nstd229human GRCh38 chr4: 183,660,824-183,661,608 , GRCh37.p13 chr4: 184,581,977-184,582,761 TRAPPC11
    nsv6744773copy number variation1nstd229human GRCh38 chr4: 183,528,600-183,785,915 , GRCh37.p13 chr4: 184,449,753-184,707,068 RWDD4, LOC101929996, 6 more genes
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