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Items: 1 to 20 of 179

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5929017copy number variation1nstd209human GRCh38 chr15: 90,926,240-90,928,342 , GRCh37.p13 chr15: 91,469,470-91,471,572 HDDC3, UNC45A
    nsv5869183copy number variation1nstd209human GRCh38 chr15: 90,926,388-90,928,323 , GRCh37.p13 chr15: 91,469,618-91,471,553 UNC45A, HDDC3
    nsv5380768copy number variation1nstd102humanUncertain significance GRCh37 chr15: 91,290,623-91,512,067 , GRCh38.p12 chr15: 90,747,393-90,968,837 BLM, MAN2A2, 9 more genes
    nsv5009181copy number variation1nstd200human GRCh38 chr15: 90,949,020-91,019,180 , GRCh37.p13 chr15: 91,492,250-91,562,410 UNC45A, PRC1, 4 more genes
    nsv5009180copy number variation1nstd200human GRCh38 chr15: 90,925,948-90,928,224 , GRCh37.p13 chr15: 91,469,178-91,471,454 HDDC3, UNC45A
    nsv5002374copy number variation1nstd200human GRCh38 chr15: 90,946,029-90,958,116 , GRCh37.p13 chr15: 91,489,259-91,501,346 RCCD1, UNC45A
    nsv5002373copy number variation1nstd200human GRCh38 chr15: 90,944,368-90,978,695 , GRCh37.p13 chr15: 91,487,598-91,521,925 RCCD1, PRC1-AS1, 2 more genes
    nsv5002372copy number variation1nstd200human GRCh38 chr15: 90,944,276-90,954,497 , GRCh37.p13 chr15: 91,487,506-91,497,727 UNC45A, RCCD1
    nsv5002371copy number variation1nstd200human GRCh38 chr15: 90,926,288-90,928,252 , GRCh37.p13 chr15: 91,469,518-91,471,482 HDDC3, UNC45A
    nsv4732693copy number variation1nstd199human GRCh37 chr15: 91,489,292-91,489,357 , GRCh38.p12 chr15: 90,946,062-90,946,127 UNC45A
    nsv4729092copy number variation1nstd102humanPathogenic GRCh37 chr15: 86,962,053-102,531,392 , GRCh38.p12 chr15: 86,418,822-101,981,189 CHD2, MIR11181, 272 more genes
    nsv4681314copy number variation1nstd102humanUncertain significance GRCh37 chr15: 91,326,042-91,512,067 , GRCh38.p12 chr15: 90,782,812-90,968,837 MAN2A2, UNC45A, 9 more genes
    nsv4675917copy number variation1nstd102humanUncertain significance GRCh37 chr15: 91,347,599-91,491,931 , GRCh38.p12 chr15: 90,804,369-90,948,701 FES, MAN2A2, 6 more genes
    nsv4675149copy number variation1nstd102humanPathogenic GRCh37 chr15: 87,189,245-102,429,112 , GRCh38.p12 chr15: 86,646,014-101,888,909 TTLL13, LINC00052, 264 more genes
    nsv4577711mobile element insertion1nstd166human GRCh37.p13 chr15: 91,497,679-91,497,679 , GRCh38.p12 chr15: 90,954,449-90,954,449 UNC45A, RCCD1
    nsv4503352mobile element insertion1nstd166human GRCh37.p13 chr15: 91,476,240-91,476,240 , GRCh38.p12 chr15: 90,933,010-90,933,010 UNC45A, HDDC3
    nsv4457347copy number variation1nstd102humanUncertain significance GRCh37 chr15: 91,276,782-91,550,953 , GRCh38.p12 chr15: 90,733,551-91,007,723 BLM, MAN2A2, 10 more genes
    nsv4456778copy number variation1nstd102humanPathogenic GRCh37 chr15: 91,229,877-93,677,014 , GRCh38.p12 chr15: 90,686,646-93,133,785 H2AZ2P1, MAN2A2, 44 more genes
    nsv4456430copy number variation1nstd102humanPathogenic GRCh37 chr15: 90,288,175-102,429,112 , GRCh38.p12 chr15: 89,744,944-101,888,909 IQGAP1, LOC400464, 210 more genes
    nsv4377776copy number variation1nstd173human GRCh37 chr15: 86,980,083-93,499,239 , GRCh38.p12 chr15: 86,436,852-92,956,009 , RNU6-1111P, 136 more genes
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