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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097690copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,087,402-141,016,451 , GRCh38.p12 chr9: 128,325,123-138,121,999 REXO4, TOR1B, 324 more genes
    nsv7075268inversion1nstd229human GRCh38 chr9: 128,672,751-137,526,572 , GRCh37.p13 chr9: 131,435,030-140,421,024 PNPLA7, NSMF, 293 more genes
    nsv7071535inversion1nstd229human GRCh38 chr9: 124,246,999-128,875,010 , GRCh37.p13 chr9: 127,009,278-131,637,289 PTGES2-AS1, STXBP1, 130 more genes
    nsv6860109copy number variation1nstd229human GRCh38 chr9: 128,723,299-128,727,755 , GRCh37.p13 chr9: 131,485,578-131,490,034 ZDHHC12, ZDHHC12-DT
    nsv6860019copy number variation1nstd229human GRCh38 chr9: 128,721,801-128,940,900 , GRCh37.p13 chr9: 131,484,080-131,703,179 ENDOG, SPOUT1, 8 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
    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
    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
    nsv5251878copy number variation1nstd204human GRCh38.p13 chr9: 128,649,801-128,795,400 , GRCh37.p13 chr9: 131,412,080-131,557,679 , DYNC2I2, 9 more genes
    nsv5241889copy number variation1nstd204human GRCh38.p13 chr9: 128,441,101-129,240,100 , GRCh37.p13 chr9: 131,203,380-132,002,379 , KYAT1, 32 more genes
    nsv4769385copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,282,528-131,720,659 , GRCh38.p12 chr9: 128,520,249-128,958,380 LOC101929270, TBC1D13, 20 more genes
    nsv4675731copy number variation1nstd102humanPathogenic GRCh37 chr9: 130,957,344-132,310,210 , GRCh38.p12 chr9: 128,195,065-129,547,931 PTPA, GLE1, 55 more genes
    nsv4675555copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,094,304-131,863,858 , GRCh38.p12 chr9: 128,332,025-129,101,579 ENDOG, SPOUT1, 35 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
    nsv4455579copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,433,808-131,537,679 , GRCh38.p12 chr9: 128,671,529-128,775,400 RN7SL560P, PKN3, 4 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
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 , ABCA1, 927 more genes
    nsv4179811copy number variation1nstd166human GRCh37.p13 chr9: 131,479,585-131,509,724 , GRCh38.p12 chr9: 128,717,306-128,747,445 ZDHHC12, ZER1, 2 more genes
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