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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5918718copy number variation1nstd209human GRCh38 chr11: 94,701,514-94,721,770 , GRCh37.p13 chr11: 94,434,680-94,454,936 AMOTL1, PIWIL4-AS1
    nsv5912660copy number variation1nstd209human GRCh38 chr11: 94,872,546-94,874,043 , GRCh37.p13 chr11: 94,605,711-94,607,208 AMOTL1
    nsv5852928copy number variation1nstd209human GRCh38 chr11: 94,872,619-94,874,055 , GRCh37.p13 chr11: 94,605,784-94,607,220 AMOTL1
    nsv5851988copy number variation1nstd209human GRCh38 chr11: 94,701,498-94,715,467 , GRCh37.p13 chr11: 94,434,664-94,448,633 PIWIL4-AS1, AMOTL1
    nsv5712932mobile element insertion2nstd211human GRCh38 chr11: 94,784,137-94,784,137 , GRCh37.p13 chr11: 94,517,303-94,517,303 AMOTL1
    nsv5672640copy number variation1nstd102humanPathogenic GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976 HSPD1P13, CARD17P, 239 more genes
    nsv5598809copy number variation1nstd207human GRCh38 chr11: 94,750,515-94,750,594 , GRCh37.p13 chr11: 94,483,681-94,483,760 , AMOTL1
    nsv5506480copy number variation1nstd206human GRCh38 chr11: 94,750,515-94,750,595 , GRCh37.p13 chr11: 94,483,681-94,483,761 , AMOTL1
    nsv5505672copy number variation1nstd206human GRCh38 chr11: 94,828,300-94,828,386 , GRCh37.p13 chr11: 94,561,466-94,561,552 AMOTL1
    nsv5505575copy number variation1nstd206human GRCh38 chr11: 94,822,896-94,852,948 , GRCh37.p13 chr11: 94,556,062-94,586,113 AMOTL1
    nsv5503687copy number variation1nstd206human GRCh38 chr11: 94,768,580-94,768,968 , GRCh37.p13 chr11: 94,501,746-94,502,134 AMOTL1
    nsv5501103copy number variation1nstd206human GRCh38 chr11: 94,689,320-94,704,773 , GRCh37.p13 chr11: 94,422,486-94,437,939 PIWIL4-AS1, AMOTL1
    nsv5497096copy number variation1nstd206human GRCh38 chr11: 94,717,990-94,726,765 , GRCh37.p13 chr11: 94,451,156-94,459,931 AMOTL1, PIWIL4-AS1
    nsv5400977mobile element insertion1nstd206human GRCh38 chr11: 94,784,137-94,784,152 , GRCh37.p13 chr11: 94,517,303-94,517,318 AMOTL1
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5373810translocation1nstd200human GRCh38 chr11: 94,809,211-94,809,211 , GRCh38 chr11: 94,810,725-94,810,725 , GRCh37.p13 chr11: 94,543,891-94,543,891 , GRCh37.p13 chr11: 94,542,377-94,542,377 AMOTL1
    nsv5373809translocation1nstd200human GRCh38 chr11: 94,803,431-94,803,431 , GRCh38 chr11: 94,814,336-94,814,336 , GRCh37.p13 chr11: 94,536,597-94,536,597 , GRCh37.p13 chr11: 94,547,502-94,547,502 AMOTL1
    nsv5348137translocation1nstd200human GRCh38 chr11: 94,823,453-94,823,453 , GRCh38 chr11: 94,693,274-94,693,274 , GRCh37.p13 chr11: 94,426,440-94,426,440 , GRCh37.p13 chr11: 94,556,619-94,556,619 PIWIL4-AS1, AMOTL1
    nsv5331190translocation1nstd200human GRCh37 chr11: 94,426,440-94,426,440 , GRCh37 chr11: 94,556,619-94,556,619 , GRCh38.p12 chr11: 94,823,453-94,823,453 , GRCh38.p12 chr11: 94,693,274-94,693,274 PIWIL4-AS1, AMOTL1
    nsv5274802copy number variation1nstd204human GRCh38.p13 chr11: 94,711,601-94,719,700 , GRCh37.p13 chr11: 94,444,767-94,452,866 PIWIL4-AS1, AMOTL1
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