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Items: 1 to 20 of 175

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5952196insertion1nstd209human GRCh38 chr9: 127,720,831-127,720,831 , GRCh37.p13 chr9: 130,483,110-130,483,110 TTC16
    nsv5629036insertion1nstd207human GRCh38 chr9: 127,720,831-127,720,831 , GRCh37.p13 chr9: 130,483,110-130,483,110 TTC16
    nsv5564479copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr9: 129,376,729-131,016,993 , GRCh38.p12 chr9: 126,614,450-128,254,714 PIP5KL1, MIR3911, 50 more genes
    nsv5243983copy number variation1nstd204human GRCh38.p13 chr9: 127,720,701-128,119,000 , GRCh37.p13 chr9: 130,482,980-130,881,279 MIR2861, ENG, 21 more genes
    nsv4985732copy number variation1nstd200human GRCh38 chr9: 127,723,305-127,742,846 , GRCh37.p13 chr9: 130,485,584-130,505,125 SH2D3C, TOR2A, 1 more genes
    nsv4983730copy number variation1nstd200human GRCh38 chr9: 127,719,987-127,722,515 , GRCh37.p13 chr9: 130,482,266-130,484,794 TTC16
    nsv4841906copy number variation1nstd200human GRCh37 chr9: 130,482,266-130,484,794 , GRCh38.p12 chr9: 127,719,987-127,722,515 TTC16
    nsv4841650copy number variation1nstd200human GRCh37 chr9: 130,485,584-130,505,125 , GRCh38.p12 chr9: 127,723,305-127,742,846 TOR2A, TTC16, 1 more genes
    nsv4768374copy number variation1nstd102humanPathogenic GRCh37 chr9: 130,412,438-131,423,964 , GRCh38.p12 chr9: 127,650,159-128,661,685 COQ4, GLE1, 53 more genes
    nsv4768372copy number variation1nstd102humanPathogenic GRCh37 chr9: 128,512,347-130,702,572 , GRCh38.p12 chr9: 125,750,068-127,940,293 LOC105379841, PTRH1, 47 more genes
    nsv4752071insertion1nstd199human GRCh37 chr9: 130,483,076-130,483,076 , GRCh38.p12 chr9: 127,720,797-127,720,797 TTC16
    nsv4685697copy number variation1nstd102humanPathogenic GRCh37 chr9: 130,435,492-130,485,618 , GRCh38.p12 chr9: 127,673,213-127,723,339 CFAP157, MIR3911, 3 more genes
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4450425copy number variation2nstd102humanPathogenic GRCh37 chr9: 130,374,663-131,329,276 , GRCh38 chr9: 127,612,384-128,566,997 RNU7-171P, MIR2861, 50 more genes
    nsv4450184copy number variation1nstd102humanUncertain significance GRCh37 chr9: 130,216,797-130,953,151 , GRCh38 chr9: 127,454,518-128,190,872 TTC16, FPGS, 32 more genes
    nsv4448099insertion1nstd175human GRCh37 chr9: 130,483,078-130,483,078 , GRCh38.p12 chr9: 127,720,799-127,720,799 TTC16
    nsv4350379copy number variation1nstd102humanPathogenic GRCh37 chr9: 130,335,766-130,517,907 , GRCh38.p12 chr9: 127,573,487-127,755,628 STXBP1, SH2D3C, 6 more genes
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 , ABCA1, 927 more genes
    nsv4191341copy number variation1nstd166human GRCh37.p13 chr9: 130,477,900-130,485,000 , GRCh38.p12 chr9: 127,715,621-127,722,721 CFAP157, PTRH1, 1 more genes
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