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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5941188copy number variation1nstd209human GRCh38 chr18: 73,348,577-73,349,080 , GRCh37.p13 chr18: 71,015,812-71,016,315 LINC02582
    nsv5936868copy number variation1nstd209human GRCh38 chr18: 73,348,957-73,354,799 , GRCh37.p13 chr18: 71,016,192-71,022,034 LINC02582
    nsv5935502copy number variation1nstd209human GRCh38 chr18: 73,335,192-73,336,776 , GRCh37.p13 chr18: 71,002,427-71,004,011 LINC02582
    nsv5933851copy number variation1nstd209human GRCh38 chr18: 73,332,579-73,340,253 , GRCh37.p13 chr18: 70,999,814-71,007,488 LINC02582
    nsv5883362copy number variation1nstd209human GRCh38 chr18: 73,335,401-73,336,700 , GRCh37.p13 chr18: 71,002,636-71,003,935 LINC02582
    nsv5877148copy number variation1nstd209human GRCh38 chr18: 73,324,553-73,326,978 , GRCh37.p13 chr18: 70,991,788-70,994,213 LINC02582
    nsv5870411copy number variation1nstd209human GRCh38 chr18: 73,348,905-73,354,797 , GRCh37.p13 chr18: 71,016,140-71,022,032 LINC02582
    nsv5705883mobile element insertion1nstd211human GRCh38 chr18: 73,332,920-73,332,920 , GRCh37.p13 chr18: 71,000,155-71,000,155 LINC02582
    nsv5651696insertion1nstd207human GRCh38 chr18: 73,347,721-73,347,721 , GRCh37.p13 chr18: 71,014,956-71,014,956 LINC02582
    nsv5519484copy number variation1nstd206human GRCh38 chr18: 73,212,274-73,711,935 , GRCh37.p13 chr18: 70,879,509-71,379,170 LINC02582, LINC02864, 1 more genes
    nsv5517953copy number variation1nstd206human GRCh38 chr18: 73,335,191-73,336,829 , GRCh37.p13 chr18: 71,002,426-71,004,064 LINC02582
    nsv5515613copy number variation1nstd206human GRCh38 chr18: 73,324,966-73,330,281 , GRCh37.p13 chr18: 70,992,201-70,997,516 LINC02582
    nsv5514135copy number variation1nstd206human GRCh38 chr18: 62,909,528-80,261,528 , GRCh37.p13 chr18: 60,576,761-78,017,154 , SMIM21, 190 more genes
    nsv5431257mobile element insertion1nstd206human GRCh38 chr18: 73,332,920-73,332,971 , GRCh37.p13 chr18: 71,000,155-71,000,206 LINC02582
    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
    nsv5359287translocation1nstd200human GRCh38 chr18: 73,329,238-73,329,238 , GRCh38 chr18: 73,329,149-73,329,149 , GRCh37.p13 chr18: 70,996,384-70,996,384 , GRCh37.p13 chr18: 70,996,473-70,996,473 LINC02582
    nsv5290962copy number variation1nstd204human GRCh38.p13 chr18: 73,334,801-73,336,750 , GRCh37.p13 chr18: 71,002,036-71,003,985 LINC02582
    nsv5027116copy number variation1nstd200human GRCh38 chr18: 73,349,599-73,358,221 , GRCh37.p13 chr18: 71,016,834-71,025,456 LINC02582
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