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Items: 1 to 20 of 258

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv5942329copy number variation1nstd209human GRCh38 chr18: 31,526,323-31,526,430 , GRCh37.p13 chr18: 29,106,286-29,106,393 DSG2
    nsv5717662mobile element insertion1nstd211human GRCh38 chr18: 31,542,161-31,542,161 , GRCh37.p13 chr18: 29,122,124-29,122,124 DSG2-AS1, DSG2
    nsv5711741mobile element insertion1nstd211human GRCh38 chr18: 31,519,960-31,519,960 , GRCh37.p13 chr18: 29,099,923-29,099,923 DSG2
    nsv5673140copy number variation1nstd102humanPathogenic GRCh38 chr18: 31,545,864-31,546,096 , GRCh37 chr18: 29,125,827-29,126,059 DSG2-AS1, DSG2
    nsv5562656mobile element insertion1nstd206human GRCh38 chr18: 31,542,161-31,542,212 , GRCh37.p13 chr18: 29,122,124-29,122,175 DSG2, DSG2-AS1
    nsv5526156copy number variation1nstd206human GRCh38 chr18: 31,526,326-31,526,431 , GRCh37.p13 chr18: 29,106,289-29,106,394 DSG2
    nsv5524104copy number variation1nstd206human GRCh38 chr18: 31,528,628-31,528,847 , GRCh37.p13 chr18: 29,108,591-29,108,810 DSG2
    nsv5519081copy number variation1nstd206human GRCh38 chr18: 31,538,984-31,539,044 , GRCh37.p13 chr18: 29,118,947-29,119,007 DSG2
    nsv5421649mobile element insertion1nstd206human GRCh38 chr18: 31,519,960-31,520,011 , GRCh37.p13 chr18: 29,099,923-29,099,974 DSG2
    nsv5381260copy number variation1nstd102humanUncertain significance GRCh37 chr18: 29,118,704-29,126,716 , GRCh38.p12 chr18: 31,538,741-31,546,753 DSG2-AS1, DSG2
    nsv5024038copy number variation1nstd200human GRCh38 chr18: 28,435,232-32,096,725 , GRCh37.p13 chr18: 26,015,196-29,676,688 DSC2, LOC100287539, 35 more genes
    nsv5011180copy number variation1nstd200human GRCh38 chr18: 31,531,926-31,532,040 , GRCh37.p13 chr18: 29,111,889-29,112,003 DSG2
    nsv5011179copy number variation1nstd200human GRCh38 chr18: 31,517,695-31,518,700 , GRCh37.p13 chr18: 29,097,658-29,098,663 DSG2
    nsv5011178copy number variation1nstd200human GRCh38 chr18: 31,505,929-31,506,985 , GRCh37.p13 chr18: 29,085,892-29,086,948 DSG2
    nsv4859145copy number variation1nstd200human GRCh37 chr18: 29,097,658-29,098,663 , GRCh38.p12 chr18: 31,517,695-31,518,700 DSG2
    nsv4859144copy number variation1nstd200human GRCh37 chr18: 29,085,899-29,086,941 , GRCh38.p12 chr18: 31,505,936-31,506,978 DSG2
    nsv4729939copy number variation1nstd102humanUncertain significance GRCh37 chr18: 25,329,706-29,734,723 , GRCh38.p12 chr18: 27,749,742-32,154,760 SLC25A52, LOC105372043, 37 more genes
    nsv4729854copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,971,647-33,737,300 , GRCh38.p12 chr18: 26,391,683-36,157,337 CLUHP6, KLHL14, 100 more genes
    nsv4682667copy number variation1nstd102humanUncertain significance GRCh37 chr18: 28,647,971-29,178,648 , GRCh38.p12 chr18: 31,068,005-31,598,685 DSC1, TTR, 10 more genes
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