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Items: 1 to 20 of 128

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5927101copy number variation1nstd209human GRCh38 chr10: 73,109,278-73,109,343 , GRCh37.p13 chr10: 74,869,036-74,869,101 NUDT13
    nsv5914351copy number variation1nstd209human GRCh38 chr10: 73,109,301-73,109,473 , GRCh37.p13 chr10: 74,869,059-74,869,231 NUDT13
    nsv5909992copy number variation1nstd209human GRCh38 chr10: 72,964,663-80,533,256 , GRCh37.p13 chr10: 74,724,421-82,293,012 , PRXL2A, 155 more genes
    nsv5696261mobile element insertion1nstd211human GRCh38 chr10: 73,128,404-73,128,404 , GRCh37.p13 chr10: 74,888,162-74,888,162 NUDT13
    nsv5550149insertion1nstd206human GRCh38 chr10: 73,112,366-73,112,404 , GRCh37.p13 chr10: 74,872,124-74,872,162 NUDT13
    nsv5399418mobile element insertion1nstd206human GRCh38 chr10: 73,128,404-73,128,455 , GRCh37.p13 chr10: 74,888,162-74,888,213 NUDT13
    nsv5126780mobile element insertion1nstd203human GRCh38 chr10: 73,112,353-73,112,366 , GRCh37.p13 chr10: 74,872,111-74,872,124 NUDT13
    nsv5124855mobile element insertion1nstd203human GRCh38 chr10: 73,128,389-73,128,404 , GRCh37.p13 chr10: 74,888,147-74,888,162 NUDT13
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4976527copy number variation1nstd200human GRCh38 chr10: 73,127,255-73,130,302 , GRCh37.p13 chr10: 74,887,013-74,890,060 NUDT13
    nsv4832062copy number variation1nstd200human GRCh37 chr10: 74,887,013-74,890,060 , GRCh38.p12 chr10: 73,127,255-73,130,302 NUDT13
    nsv4756674insertion1nstd199human GRCh37 chr10: 74,872,104-74,872,104 , GRCh38.p12 chr10: 73,112,346-73,112,346 NUDT13
    nsv4748684copy number variation1nstd199human GRCh37 chr10: 74,878,851-74,878,984 , GRCh38.p12 chr10: 73,119,093-73,119,226 NUDT13
    nsv4576911mobile element insertion1nstd166human GRCh37.p13 chr10: 74,875,622-74,875,622 , GRCh38.p12 chr10: 73,115,864-73,115,864 NUDT13
    nsv4547743insertion1nstd166human GRCh37.p13 chr10: 74,872,111-74,872,111 , GRCh38.p12 chr10: 73,112,353-73,112,353 NUDT13
    nsv4491363mobile element insertion1nstd166human GRCh37.p13 chr10: 74,888,147-74,888,147 , GRCh38.p12 chr10: 73,128,389-73,128,389 NUDT13
    nsv4343722sequence alteration1nstd166human GRCh37.p13 chr10: 43,905,894-92,001,956 , GRCh38.p12 chr10: 43,410,446-90,242,199 , ALOX5, 749 more genes
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4185380copy number variation1nstd166human GRCh37.p13 chr10: 74,869,106-74,869,195 , GRCh38.p12 chr10: 73,109,348-73,109,437 NUDT13
    nsv3970675copy number variation1nstd168human GRCh38 chr10: 73,032,091-73,180,232 , GRCh37.p13 chr10: 74,791,849-74,939,990 ECD, NUDT13, 3 more genes
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