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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
    nsv5969313inversion1nstd209human GRCh38 chr18: 49,148,257-52,144,553 , GRCh37.p13 chr18: 46,674,627-49,670,923 , SMAD4, 52 more genes
    nsv5936882copy number variation1nstd209human GRCh38 chr18: 50,924,452-50,924,531 , GRCh37.p13 chr18: 48,450,822-48,450,901 ME2
    nsv5728390mobile element insertion1nstd211human GRCh38 chr18: 50,953,447-50,953,447 , GRCh37.p13 chr18: 48,479,817-48,479,817 ME2
    nsv5722027mobile element insertion2nstd211human GRCh38 chr18: 50,945,620-50,945,620 , GRCh37.p13 chr18: 48,471,990-48,471,990 ME2
    nsv5716150mobile element insertion1nstd211human GRCh38 chr18: 50,918,222-50,918,222 , GRCh37.p13 chr18: 48,444,592-48,444,592 ME2
    nsv5653215insertion1nstd207human GRCh38 chr18: 50,924,452-50,924,452 , GRCh37.p13 chr18: 48,450,822-48,450,822 ME2
    nsv5564037mobile element insertion1nstd206human GRCh38 chr18: 50,953,447-50,953,498 , GRCh37.p13 chr18: 48,479,817-48,479,868 ME2
    nsv5556025mobile element insertion1nstd206human GRCh38 chr18: 50,945,620-50,945,671 , GRCh37.p13 chr18: 48,471,990-48,472,041 ME2
    nsv5525129copy number variation1nstd206human GRCh38 chr18: 50,904,148-50,913,499 , GRCh37.p13 chr18: 48,430,518-48,439,869 ME2
    nsv5183957mobile element insertion1nstd203human GRCh38 chr18: 50,918,222-50,918,239 , GRCh37.p13 chr18: 48,444,592-48,444,609 ME2
    nsv5018059copy number variation1nstd200human GRCh38 chr18: 50,952,611-50,964,297 , GRCh37.p13 chr18: 48,478,981-48,490,667 ME2
    nsv5018058copy number variation1nstd200human GRCh38 chr18: 50,905,624-50,905,757 , GRCh37.p13 chr18: 48,431,994-48,432,127 ME2
    nsv4859616copy number variation1nstd200human GRCh37 chr18: 48,469,434-48,469,785 , GRCh38.p12 chr18: 50,943,064-50,943,415 ME2
    nsv4859615copy number variation1nstd200human GRCh37 chr18: 48,431,994-48,432,127 , GRCh38.p12 chr18: 50,905,624-50,905,757 ME2
    nsv4735269copy number variation1nstd199human GRCh37 chr18: 48,467,394-48,467,460 , GRCh38.p12 chr18: 50,941,024-50,941,090 ME2
    nsv4708366copy number variation1nstd195human GRCh37 chr18: 48,467,720-48,467,721 , GRCh38.p12 chr18: 50,941,350-50,941,351 ME2
    nsv4679055copy number variation1nstd189human GRCh37.p13 chr18: 48,222,317-48,666,871 , GRCh38.p12 chr18: 50,695,947-51,140,501 , SMAD4, 8 more genes
    nsv4676155copy number variation1nstd102humanPathogenic GRCh37 chr18: 20,689,919-49,455,212 , GRCh38.p12 chr18: 23,109,955-51,928,842 KLHL14, RPL23AP77, 318 more genes
    nsv4578035mobile element insertion1nstd166human GRCh37.p13 chr18: 48,444,592-48,444,592 , GRCh38.p12 chr18: 50,918,222-50,918,222 ME2
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