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Items: 1 to 20 of 465

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6118583copy number variation1nstd186human GRCh37 chr1: 161,546,377-161,632,377 , GRCh38.p12 chr1: 161,576,587-161,662,587 FCGR2B, FCGR3B, 4 more genes
    nsv5969343inversion1nstd209human GRCh38 chr1: 161,566,673-161,918,703 , GRCh37.p13 chr1: 161,536,463-161,888,493 FCGR2B, FCGR3B, 12 more genes
    nsv5885335copy number variation1nstd209human GRCh38 chr1: 161,616,629-161,616,937 , GRCh37.p13 chr1: 161,586,419-161,586,727 RPS23P9
    nsv5880515copy number variation1nstd209human GRCh38 chr1: 161,579,290-161,661,012 , GRCh37.p13 chr1: 161,549,080-161,630,802 FCGR2B, FCGR3B, 4 more genes
    nsv5828388copy number variation2nstd209human GRCh38 chr1: 161,618,093-161,627,255 , GRCh37.p13 chr1: 161,587,883-161,597,045 FCGR3B, RPS23P9
    nsv5828387copy number variation2nstd209human GRCh38 chr1: 161,614,993-161,616,583 , GRCh37.p13 chr1: 161,584,783-161,586,373 RPS23P9
    nsv5828070copy number variation2nstd209human GRCh38 chr1: 161,600,299-161,624,511 , GRCh37.p13 chr1: 161,570,089-161,594,301 FCGR3B, HSPA7, 3 more genes
    nsv5575099copy number variation1nstd207human GRCh38 chr1: 161,571,558-161,653,408 , GRCh37.p13 chr1: 161,541,348-161,623,198 FCGR2B, FCGR3B, 4 more genes
    nsv5569480copy number variation1nstd207human GRCh38 chr1: 161,615,949-161,617,423 , GRCh37.p13 chr1: 161,585,739-161,587,213 RPS23P9
    nsv5421696copy number variation1nstd206human GRCh38 chr1: 161,576,587-161,662,587 , GRCh37.p13 chr1: 161,546,377-161,632,377 FCGR2B, FCGR3B, 4 more genes
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5217131copy number variation1nstd204human GRCh37.p13 chr1: 161,558,991-161,615,690 , GRCh38.p13 chr1: 161,589,201-161,645,900 FCGR2B, FCGR3B, 4 more genes
    nsv5215677copy number variation1nstd204human GRCh37.p13 chr1: 161,533,991-161,637,390 , GRCh38.p13 chr1: 161,564,201-161,667,600 FCGR2B, FCGR3B, 4 more genes
    nsv5213822copy number variation1nstd204human GRCh38.p13 chr1: 161,610,246-161,623,651 , GRCh37.p13 chr1: 161,580,036-161,593,441 RPS23P9, TRL-CAA6-1, 1 more genes
    nsv5213008copy number variation1nstd204human GRCh38.p13 chr1: 161,611,501-161,628,400 , GRCh37.p13 chr1: 161,581,291-161,598,190 RPS23P9, TRL-CAA6-1, 1 more genes
    nsv5212435copy number variation1nstd204human GRCh38.p13 chr1: 161,600,201-161,628,800 , GRCh37.p13 chr1: 161,569,991-161,598,590 FCGR3B, RPS23P9, 3 more genes
    nsv5209728copy number variation1nstd204human GRCh38.p13 chr1: 161,515,301-161,670,800 , GRCh37.p13 chr1: 161,485,091-161,640,590 HSPA7, FCGR3A, 13 more genes
    nsv5208602copy number variation1nstd204human GRCh38.p13 chr1: 161,600,399-161,628,177 , GRCh37.p13 chr1: 161,570,189-161,597,967 HSPA7, FCGR3B, 3 more genes
    nsv5207485copy number variation1nstd204human GRCh38.p13 chr1: 161,610,201-161,617,600 , GRCh37.p13 chr1: 161,579,991-161,587,390 RPS23P9, TRL-CAA6-1
    nsv5207221copy number variation1nstd204human GRCh37.p13 chr1: 161,538,591-161,620,590 , GRCh38.p13 chr1: 161,568,801-161,650,800 FCGR2B, FCGR3B, 4 more genes
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