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Items: 1 to 20 of 209

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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
    nsv6874102copy number variation1nstd229human GRCh38 chr9: 127,885,516-127,899,489 , GRCh37.p13 chr9: 130,647,795-130,661,768 ST6GALNAC6, AK1
    nsv6862765copy number variation1nstd229human GRCh38 chr9: 127,893,290-127,893,408 , GRCh37.p13 chr9: 130,655,569-130,655,687 ST6GALNAC6
    nsv6862108copy number variation1nstd229human GRCh38 chr9: 127,893,042-127,894,593 , GRCh37.p13 chr9: 130,655,321-130,656,872 ST6GALNAC6
    nsv6858409copy number variation1nstd229human GRCh38 chr9: 127,769,112-128,669,700 , GRCh37.p13 chr9: 130,531,391-131,431,979 BBLN, SH2D3C, 47 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6452920copy number variation1nstd223human GRCh38 chr9: 127,883,499-127,888,350 , GRCh37.p13 chr9: 130,645,778-130,650,629 AK1, ST6GALNAC6
    nsv6452614copy number variation1nstd223human GRCh38 chr9: 127,901,750-127,914,126 , GRCh37.p13 chr9: 130,664,029-130,676,405 ST6GALNAC6, ST6GALNAC4
    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
    nsv6439686copy number variation1nstd223human GRCh38 chr9: 127,893,042-127,894,589 , GRCh37.p13 chr9: 130,655,321-130,656,868 ST6GALNAC6
    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
    nsv6438566copy number variation1nstd223human GRCh38 chr9: 127,883,350-127,883,726 , GRCh37.p13 chr9: 130,645,629-130,646,005 ST6GALNAC6, AK1
    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
    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
    nsv5673957copy number variation1nstd102humanPathogenic GRCh37 chr9: 130,577,951-130,700,109 , GRCh38.p12 chr9: 127,815,672-127,937,830 DPM2, ENG, 8 more genes
    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
    nsv5493473copy number variation1nstd206human GRCh38 chr9: 127,883,350-127,883,726 , GRCh37.p13 chr9: 130,645,629-130,646,005 AK1, ST6GALNAC6
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