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Items: 1 to 20 of 325

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130241insertion1nstd186human GRCh37 chr18: 55,120,818-55,120,867 , GRCh38.p12 chr18: 57,453,586-57,453,635 , ONECUT2
    nsv6112815copy number variation1nstd102humanPathogenic GRCh37 chr18: 54,285,235-77,960,815 , GRCh38.p12 chr18: 56,618,004-80,202,932 RPL31P9, TRG-TCC5-1, 271 more genes
    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
    nsv5976912insertion1nstd209human GRCh38 chr18: 57,453,584-57,453,584 , GRCh37.p13 chr18: 55,120,816-55,120,816 , ONECUT2
    nsv5713437mobile element insertion1nstd211human GRCh38 chr18: 57,470,638-57,470,638 , GRCh37.p13 chr18: 55,137,870-55,137,870 ONECUT2
    nsv5698746mobile element insertion1nstd211human GRCh38 chr18: 57,445,592-57,445,592 , GRCh37.p13 chr18: 55,112,824-55,112,824 , ONECUT2
    nsv5656976insertion1nstd207human GRCh38 chr18: 57,453,584-57,453,584 , GRCh37.p13 chr18: 55,120,816-55,120,816 , ONECUT2
    nsv5545478insertion1nstd206human GRCh38 chr18: 57,453,586-57,453,635 , GRCh37.p13 chr18: 55,120,818-55,120,867 , ONECUT2
    nsv5543117insertion1nstd206human GRCh38 chr18: 57,459,939-57,459,973 , GRCh37.p13 chr18: 55,127,171-55,127,205 , ONECUT2
    nsv5518381copy number variation1nstd206human GRCh38 chr18: 57,457,066-57,458,530 , GRCh37.p13 chr18: 55,124,298-55,125,762 , ONECUT2
    nsv5416501mobile element insertion1nstd206human GRCh38 chr18: 57,470,638-57,470,689 , GRCh37.p13 chr18: 55,137,870-55,137,921 ONECUT2
    nsv5381802copy number variation1nstd102humanPathogenic GRCh37 chr18: 51,925,586-78,010,032 , GRCh38.p12 chr18: 54,399,216-80,252,149 LOC105372200, LOC105372174, 298 more genes
    nsv5359150translocation1nstd200human GRCh38 chr18: 57,462,815-57,462,815 , GRCh38 chr18: 57,462,519-57,462,519 , GRCh37.p13 chr18: 55,129,751-55,129,751 , GRCh37.p13 chr18: 55,130,047-55,130,047 , ONECUT2
    nsv5359149translocation1nstd200human GRCh38 chr18: 57,441,400-57,441,400 , GRCh38 chr18: 57,438,400-57,438,400 , GRCh37.p13 chr18: 55,105,632-55,105,632 , GRCh37.p13 chr18: 55,108,632-55,108,632 , ONECUT2
    nsv5188054mobile element insertion1nstd203human GRCh38 chr18: 57,480,744-57,480,751 , GRCh37.p13 chr18: 55,147,976-55,147,983 ONECUT2
    nsv4766668insertion1nstd199human GRCh37 chr18: 55,120,810-55,120,810 , GRCh38.p12 chr18: 57,453,578-57,453,578 , ONECUT2
    nsv4730003copy number variation1nstd102humanUncertain significance GRCh37 chr18: 55,040,694-55,858,630 , GRCh38.p12 chr18: 57,373,463-58,191,398 LOC105372143, LOC105372140, 13 more genes
    nsv4718742insertion1nstd186human GRCh37 chr18: 55,120,816-55,120,816 , GRCh38.p12 chr18: 57,453,584-57,453,584 , ONECUT2
    nsv4676235copy number variation1nstd102humanUncertain significance GRCh37 chr18: 54,552,231-55,285,563 , GRCh38.p12 chr18: 56,885,000-57,618,331 LOC105372136, WDR7-OT1, 9 more genes
    nsv4676212copy number variation1nstd102humanUncertain significance GRCh37 chr18: 54,652,730-55,528,259 , GRCh38.p12 chr18: 56,985,499-57,861,027 FECH, WDR7, 17 more genes
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