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Items: 1 to 20 of 152

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5913674copy number variation1nstd209human GRCh38 chr9: 92,757,932-92,758,279 , GRCh37.p13 chr9: 95,520,214-95,520,561 BICD2
    nsv5715959mobile element insertion1nstd211human GRCh38 chr9: 92,754,925-92,754,925 , GRCh37.p13 chr9: 95,517,207-95,517,207 BICD2
    nsv5712490mobile element insertion2nstd211human GRCh38 chr9: 92,762,261-92,762,261 , GRCh37.p13 chr9: 95,524,543-95,524,543 BICD2
    nsv5696068mobile element insertion1nstd211human GRCh38 chr9: 92,751,136-92,751,136 , GRCh37.p13 chr9: 95,513,418-95,513,418 BICD2
    nsv5563961mobile element insertion1nstd206human GRCh38 chr9: 92,754,925-92,754,930 , GRCh37.p13 chr9: 95,517,207-95,517,212 BICD2
    nsv5562344sequence alteration1nstd206human GRCh38 chr9: 92,266,854-92,881,037 , GRCh37.p13 chr9: 95,029,136-95,643,319 ECM2, BICD2, 21 more genes
    nsv5477942copy number variation1nstd206human GRCh38 chr9: 92,721,200-92,721,276 , GRCh37.p13 chr9: 95,483,482-95,483,558 BICD2
    nsv5396583mobile element insertion1nstd206human GRCh38 chr9: 92,762,261-92,762,312 , GRCh37.p13 chr9: 95,524,543-95,524,594 BICD2
    nsv5381661copy number variation1nstd102humanUncertain significance GRCh37 chr9: 95,526,777-95,527,036 , GRCh38.p12 chr9: 92,764,495-92,764,754 BICD2
    nsv5372807translocation1nstd200human GRCh38 chr9: 92,751,827-92,751,827 , GRCh38 chr9: 92,753,058-92,753,058 , GRCh37.p13 chr9: 95,515,340-95,515,340 , GRCh37.p13 chr9: 95,514,109-95,514,109 BICD2
    nsv5138642mobile element insertion1nstd203human GRCh38 chr9: 92,762,239-92,762,256 , GRCh37.p13 chr9: 95,524,521-95,524,538 BICD2
    nsv4974710copy number variation1nstd200human GRCh38 chr9: 92,739,291-92,806,321 , GRCh37.p13 chr9: 95,501,573-95,568,603 LOC101929748, BICD2
    nsv4973194copy number variation1nstd200human GRCh38 chr9: 92,764,955-92,765,088 , GRCh37.p13 chr9: 95,527,237-95,527,370 BICD2
    nsv4973193copy number variation1nstd200human GRCh38 chr9: 92,756,932-92,764,032 , GRCh37.p13 chr9: 95,519,214-95,526,314 BICD2
    nsv4973192copy number variation1nstd200human GRCh38 chr9: 92,734,924-92,734,996 , GRCh37.p13 chr9: 95,497,206-95,497,278 BICD2
    nsv4887530inversion1nstd200human GRCh37 chr9: 90,662,371-96,951,001 , GRCh38.p12 chr9: 88,047,456-94,188,719 , MTATP6P29, 125 more genes
    nsv4814861copy number variation1nstd200human GRCh37 chr9: 95,501,573-95,568,603 , GRCh38.p12 chr9: 92,739,291-92,806,321 LOC101929748, BICD2
    nsv4814492copy number variation1nstd200human GRCh37 chr9: 95,497,206-95,497,278 , GRCh38.p12 chr9: 92,734,924-92,734,996 BICD2
    nsv4717168mobile element insertion1nstd186human GRCh37 chr9: 95,524,521-95,524,521 , GRCh38.p12 chr9: 92,762,239-92,762,239 BICD2
    nsv4682514copy number variation1nstd102humanUncertain significance GRCh38 chr9: 92,715,417-92,717,040 , GRCh37 chr9: 95,477,699-95,479,322 BICD2
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