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Items: 1 to 20 of 265

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5921766copy number variation1nstd209human GRCh38 chr11: 47,715,819-47,715,928 , GRCh37.p13 chr11: 47,737,371-47,737,480 FNBP4, AGBL2
    nsv5919416copy number variation1nstd209human GRCh38 chr11: 47,753,956-47,754,264 , GRCh37.p13 chr11: 47,775,508-47,775,816 FNBP4
    nsv5916129copy number variation1nstd209human GRCh38 chr11: 47,740,285-47,741,685 , GRCh37.p13 chr11: 47,761,837-47,763,237 FNBP4
    nsv5910020copy number variation1nstd209human GRCh38 chr11: 47,741,523-47,743,240 , GRCh37.p13 chr11: 47,763,075-47,764,792 FNBP4
    nsv5861954copy number variation1nstd209human GRCh38 chr11: 47,741,539-47,743,238 , GRCh37.p13 chr11: 47,763,091-47,764,790 FNBP4
    nsv5849525copy number variation1nstd209human GRCh38 chr11: 47,740,289-47,741,688 , GRCh37.p13 chr11: 47,761,841-47,763,240 FNBP4
    nsv5848335copy number variation1nstd209human GRCh38 chr11: 47,746,589-47,748,319 , GRCh37.p13 chr11: 47,768,141-47,769,871 FNBP4
    nsv5706494mobile element insertion1nstd211human GRCh38 chr11: 47,731,138-47,731,138 , GRCh37.p13 chr11: 47,752,690-47,752,690 FNBP4
    nsv5595965copy number variation1nstd207human GRCh38 chr11: 47,746,929-47,750,845 , GRCh37.p13 chr11: 47,768,481-47,772,397 FNBP4
    nsv5592422copy number variation1nstd207human GRCh38 chr11: 47,740,285-47,741,685 , GRCh37.p13 chr11: 47,761,837-47,763,237 FNBP4
    nsv5511910copy number variation1nstd206human GRCh38 chr11: 47,740,318-47,741,686 , GRCh37.p13 chr11: 47,761,870-47,763,238 FNBP4
    nsv5511159copy number variation1nstd206human GRCh38 chr11: 47,746,929-47,750,849 , GRCh37.p13 chr11: 47,768,481-47,772,401 FNBP4
    nsv5403127mobile element insertion1nstd206human GRCh38 chr11: 47,731,138-47,731,189 , GRCh37.p13 chr11: 47,752,690-47,752,741 FNBP4
    nsv5389560copy number variation2nstd186human GRCh37 chr11: 47,761,869-47,763,238 , GRCh38.p12 chr11|NW_019805496.1: 172,684-174,053 , GRCh38.p12 chr11: 47,740,317-47,741,686 FNBP4
    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
    nsv5380725copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr11: 45,827,353-47,804,770 , GRCh38.p12 chr11: 45,805,802-47,783,218 MIR4688, LOC112268075, 58 more genes
    nsv5309996copy number variation1nstd204human GRCh38.p13 chr11: 47,740,228-47,741,720 , GRCh37.p13 chr11: 47,761,780-47,763,272 FNBP4
    nsv5303669copy number variation1nstd204human GRCh37.p13 chr11: 47,683,149-47,985,744 , GRCh38.p13 chr11: 47,661,597-47,964,192 NUP160, FNBP4, 4 more genes
    nsv5277820copy number variation1nstd204human GRCh38.p13 chr11: 47,707,381-47,783,384 , GRCh37.p13 chr11: 47,728,933-47,804,936 NUP160, AGBL2, 1 more genes
    nsv5277697copy number variation1nstd204human GRCh38.p13 chr11: 47,740,101-47,743,900 , GRCh37.p13 chr11: 47,761,653-47,765,452 FNBP4
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