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Items: 1 to 20 of 106

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5971593insertion1nstd209human GRCh38 chr20: 16,735,298-16,735,298 , GRCh37.p13 chr20: 16,715,943-16,715,943 SNRPB2
    nsv5700160mobile element insertion1nstd211human GRCh38 chr20: 16,742,170-16,742,170 , GRCh37.p13 chr20: 16,722,815-16,722,815 SNRPB2
    nsv5666909insertion1nstd207human GRCh38 chr20: 16,735,298-16,735,298 , GRCh37.p13 chr20: 16,715,943-16,715,943 SNRPB2
    nsv5539233insertion1nstd206human GRCh38 chr20: 16,735,331-16,735,356 , GRCh37.p13 chr20: 16,715,976-16,716,001 SNRPB2
    nsv5535207insertion1nstd206human GRCh38 chr20: 16,735,336-16,735,349 , GRCh37.p13 chr20: 16,715,981-16,715,994 SNRPB2
    nsv5533905copy number variation1nstd206human GRCh38 chr20: 16,737,619-16,737,670 , GRCh37.p13 chr20: 16,718,264-16,718,315 SNRPB2
    nsv5530660copy number variation1nstd206human GRCh38 chr20: 16,704,017-17,308,202 , GRCh37.p13 chr20: 16,684,662-17,288,847 PCSK2, SNRPB2, 6 more genes
    nsv5423539mobile element insertion1nstd206human GRCh38 chr20: 16,742,170-16,742,221 , GRCh37.p13 chr20: 16,722,815-16,722,866 SNRPB2
    nsv5350170translocation1nstd200human GRCh38 chr20: 16,729,324-16,729,324 , GRCh38 chr20: 16,727,286-16,727,286 , GRCh37.p13 chr20: 16,709,969-16,709,969 , GRCh37.p13 chr20: 16,707,931-16,707,931 SNRPB2
    nsv5173585mobile element insertion1nstd203human GRCh38 chr20: 16,732,366-16,732,384 , GRCh37.p13 chr20: 16,713,011-16,713,029 SNRPB2
    nsv5025167copy number variation1nstd200human GRCh38 chr20: 16,704,017-17,308,202 , GRCh37.p13 chr20: 16,684,662-17,288,847 LOC105372544, RNU6-27P, 6 more genes
    nsv4865459copy number variation1nstd200human GRCh37 chr20: 16,684,662-17,288,847 , GRCh38.p12 chr20: 16,704,017-17,308,202 LOC105372545, LOC105372544, 6 more genes
    nsv4862189copy number variation1nstd200human GRCh37 chr20: 16,707,931-16,709,969 , GRCh38.p12 chr20: 16,727,286-16,729,324 SNRPB2
    nsv4722724insertion1nstd186human GRCh37 chr20: 16,715,943-16,715,943 , GRCh38.p12 chr20: 16,735,298-16,735,298 SNRPB2
    nsv4676419copy number variation1nstd102humanPathogenic GRCh37 chr20: 8,571,696-22,088,650 , GRCh38.p12 chr20: 8,591,049-22,108,012 PGAM3P, EEF1A1P34, 182 more genes
    nsv4676401copy number variation1nstd102humanUncertain significance GRCh37 chr20: 15,872,280-16,764,799 , GRCh38.p12 chr20: 15,891,635-16,784,154 RPL7AP13, LOC105372542, 8 more genes
    nsv4561690insertion1nstd166human GRCh37.p13 chr20: 16,715,943-16,715,943 , GRCh38.p12 chr20: 16,735,298-16,735,298 SNRPB2
    nsv4457540copy number variation1nstd102humanUncertain significance GRCh37 chr20: 16,688,627-17,288,943 , GRCh38.p12 chr20: 16,707,982-17,308,298 SNRPB2, OTOR, 6 more genes
    nsv4350090copy number variation1nstd102humanPathogenic GRCh37 chr20: 11,716,825-19,331,055 , GRCh38.p12 chr20: 11,736,177-19,350,411 ENSAP1, BANF2, 107 more genes
    nsv4349190copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,568-26,305,479 , GRCh38.p12 chr20: 80,927-26,324,843 LOC105372582, LOC101929937, 473 more genes
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