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Items: 1 to 20 of 186

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7071535inversion1nstd229human GRCh38 chr9: 124,246,999-128,875,010 , GRCh37.p13 chr9: 127,009,278-131,637,289 PTGES2-AS1, STXBP1, 130 more genes
    nsv6869761copy number variation1nstd229human GRCh38 chr9: 127,714,561-127,722,774 , GRCh37.p13 chr9: 130,476,840-130,485,053 PTRH1, TTC16, 1 more genes
    nsv6868848copy number variation1nstd229human GRCh38 chr9: 127,582,940-127,764,193 , GRCh37.p13 chr9: 130,345,219-130,526,472 MIR3911, CFAP157, 5 more genes
    nsv6862329copy number variation1nstd229human GRCh38 chr9: 127,699,401-127,703,200 , GRCh37.p13 chr9: 130,461,680-130,465,479 PTRH1
    nsv6861850copy number variation1nstd229human GRCh38 chr9: 127,695,852-127,695,902 , GRCh37.p13 chr9: 130,458,131-130,458,181 STXBP1, PTRH1
    nsv6861746copy number variation1nstd229human GRCh38 chr9: 127,697,363-127,699,758 , GRCh37.p13 chr9: 130,459,642-130,462,037 PTRH1
    nsv6860174copy number variation1nstd229human GRCh38 chr9: 127,701,636-127,707,702 , GRCh37.p13 chr9: 130,463,915-130,469,981 CFAP157, PTRH1
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6455143copy number variation1nstd223human GRCh38 chr9: 127,701,636-127,707,698 , GRCh37.p13 chr9: 130,463,915-130,469,977 PTRH1, CFAP157
    nsv6445830copy number variation1nstd223human GRCh38 chr9: 127,317,501-128,138,900 , GRCh37.p13 chr9: 130,079,780-130,901,179 STXBP1, PTGES2-AS1, 34 more genes
    nsv6440198copy number variation1nstd223human GRCh38 chr9: 127,699,381-127,703,216 , GRCh37.p13 chr9: 130,461,660-130,465,495 PTRH1
    nsv6438803copy number variation1nstd223human GRCh38 chr9: 126,485,301-128,649,400 , GRCh37.p13 chr9: 129,247,580-131,411,679 MIR199B, FPGS, 72 more genes
    nsv6314154copy number variation1nstd102humanPathogenic GRCh37 chr9: 130,306,022-130,522,616 , GRCh38.p12 chr9: 127,543,743-127,760,337 STXBP1, SH2D3C, 6 more genes
    nsv6314148copy number variation1nstd102humanPathogenic GRCh37 chr9: 130,392,953-130,526,044 , GRCh38.p12 chr9: 127,630,674-127,763,765 STXBP1, SH2D3C, 5 more genes
    nsv6314001copy number variation1nstd102humanPathogenic GRCh37 chr9: 116,422,275-131,713,233 , GRCh38.p12 chr9: 113,659,995-128,950,954 LOC105376244, RN7SL187P, 286 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6312681copy number variation1nstd102humanPathogenic GRCh37 chr9: 130,216,807-130,953,136 , GRCh38.p12 chr9: 127,454,528-128,190,857 EEIG1, PIP5KL1, 32 more genes
    nsv6303049copy number variation1nstd186human GRCh37 chr9: 130,467,274-130,467,439 , GRCh38.p12 chr9: 127,704,995-127,705,160 PTRH1, CFAP157
    nsv6291261copy number variation1nstd102humanPathogenic GRCh37 chr9: 128,523,763-132,604,808 , GRCh38.p12 chr9: 125,761,484-129,842,529 PTPA, AK1, 123 more genes
    nsv6137057copy number variation1nstd213human GRCh37 chr9: 130,360,000-135,460,001 , GRCh38.p12 chr9: 127,597,721-132,584,614 CRAT, GLE1, 145 more genes
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