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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
    nsv5972085insertion1nstd209human GRCh38 chr18: 50,237,329-50,237,329 , GRCh37.p13 chr18: 47,763,699-47,763,699 CFAP53
    nsv5969313inversion1nstd209human GRCh38 chr18: 49,148,257-52,144,553 , GRCh37.p13 chr18: 46,674,627-49,670,923 , SMAD4, 52 more genes
    nsv5943897copy number variation1nstd209human GRCh38 chr18: 50,231,749-50,238,198 , GRCh37.p13 chr18: 47,758,119-47,764,568 CFAP53
    nsv5867629copy number variation1nstd209human GRCh38 chr18: 50,235,511-50,238,022 , GRCh37.p13 chr18: 47,761,881-47,764,392 CFAP53
    nsv5559510sequence alteration1nstd206human GRCh38 chr18: 50,243,397-50,244,337 , GRCh37.p13 chr18: 47,769,767-47,770,707 CFAP53
    nsv5156530mobile element insertion1nstd203human GRCh38 chr18: 50,256,558-50,256,571 , GRCh37.p13 chr18: 47,782,928-47,782,941 CFAP53
    nsv5153792mobile element insertion1nstd203human GRCh38 chr18: 50,237,304-50,237,330 , GRCh37.p13 chr18: 47,763,674-47,763,700 CFAP53
    nsv5152077mobile element insertion1nstd203human GRCh38 chr18: 50,259,569-50,259,572 , GRCh37.p13 chr18: 47,785,939-47,785,942 CFAP53
    nsv5141941mobile element insertion1nstd203human GRCh38 chr18: 50,252,100-50,252,121 , GRCh37.p13 chr18: 47,778,470-47,778,491 CFAP53
    nsv5018037copy number variation1nstd200human GRCh38 chr18: 50,265,866-50,265,990 , GRCh37.p13 chr18: 47,792,236-47,792,360 CFAP53, MBD1
    nsv5018036copy number variation1nstd200human GRCh38 chr18: 50,231,068-50,236,201 , GRCh37.p13 chr18: 47,757,438-47,762,571 CFAP53
    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
    nsv4618867copy number variation1nstd183human GRCh37 chr18: 47,763,331-47,785,532 , GRCh38.p12 chr18: 50,236,961-50,259,162 CFAP53
    nsv4556863insertion1nstd166human GRCh37.p13 chr18: 47,785,939-47,785,939 , GRCh38.p12 chr18: 50,259,569-50,259,569 CFAP53
    nsv4514148mobile element insertion1nstd166human GRCh37.p13 chr18: 47,782,928-47,782,928 , GRCh38.p12 chr18: 50,256,558-50,256,558 CFAP53
    nsv4503397mobile element insertion1nstd166human GRCh37.p13 chr18: 47,762,453-47,762,453 , GRCh38.p12 chr18: 50,236,083-50,236,083 CFAP53
    nsv4457866copy number variation1nstd102humanPathogenic GRCh37 chr18: 45,621,155-61,416,536 , GRCh38.p12 chr18: 48,094,784-63,749,302 LOC105372159, LOC105372156, 208 more genes
    nsv4336672sequence alteration1nstd166human GRCh37.p13 chr18: 21,176,191-70,772,863 , GRCh38.p12 chr18: 23,596,227-73,105,628 , CDH2, 557 more genes
    nsv4269583copy number variation1nstd166human GRCh37.p13 chr18: 47,792,236-47,792,360 , GRCh38.p12 chr18: 50,265,866-50,265,990 CFAP53, MBD1
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