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Items: 1 to 20 of 327

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980449copy number variation1nstd102humanrisk factor GRCh37 chr3: 195,693,872-197,376,871 , GRCh38.p12 chr3: 195,967,001-197,650,000 RN7SL434P, RNU6-1279P, 54 more genes
    nsv5975867inversion1nstd209human GRCh38 chr3: 196,245,165-196,619,601 , GRCh37.p13 chr3: 195,972,036-196,346,472 PCYT1A, UBXN7, 17 more genes
    nsv5889604copy number variation1nstd209human GRCh38 chr3: 196,475,774-196,479,234 , GRCh37.p13 chr3: 196,202,645-196,206,105 RNF168
    nsv5835806copy number variation1nstd209human GRCh38 chr3: 196,475,704-196,479,162 , GRCh37.p13 chr3: 196,202,575-196,206,033 RNF168
    nsv5835198copy number variation1nstd209human GRCh38 chr3: 196,496,121-196,497,720 , GRCh37.p13 chr3: 196,222,992-196,224,591 LOC105374306, RNF168
    nsv5578552copy number variation1nstd207human GRCh38 chr3: 196,470,449-196,470,533 , GRCh37.p13 chr3: 196,197,320-196,197,404 RNF168
    nsv5574523copy number variation1nstd207human GRCh38 chr3: 196,470,185-196,470,259 , GRCh37.p13 chr3: 196,197,056-196,197,130 RNF168
    nsv5563557sequence alteration1nstd206human GRCh38 chr3: 196,244,777-196,619,867 , GRCh37.p13 chr3: 195,971,648-196,346,738 PCYT1A, FBXO45, 17 more genes
    nsv5453739copy number variation1nstd206human GRCh38 chr3: 196,475,761-196,479,196 , GRCh37.p13 chr3: 196,202,632-196,206,067 RNF168
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5450789copy number variation1nstd206human GRCh38 chr3: 196,478,836-196,478,909 , GRCh37.p13 chr3: 196,205,707-196,205,780 RNF168
    nsv5445731copy number variation1nstd206human GRCh38 chr3: 196,449,857-196,475,801 , GRCh37.p13 chr3: 196,176,728-196,202,672 UBXN7, RNF168
    nsv5441697copy number variation1nstd206human GRCh38 chr3: 196,479,651-196,479,770 , GRCh37.p13 chr3: 196,206,522-196,206,641 RNF168
    nsv5437996copy number variation1nstd206human GRCh38 chr3: 196,485,909-196,486,542 , GRCh37.p13 chr3: 196,212,780-196,213,413 RNF168
    nsv5381417copy number variation1nstd102humanUncertain significance GRCh37 chr3: 195,754,030-196,438,852 , GRCh38.p12 chr3: 196,027,159-196,711,981 PIGX, TM4SF19-DYNLT2B, 28 more genes
    nsv5237696copy number variation1nstd204human GRCh38.p13 chr3: 196,295,401-196,501,800 , GRCh37.p13 chr3: 196,022,272-196,228,671 TM4SF19, UBXN7, 11 more genes
    nsv5200370copy number variation1nstd102humanPathogenic GRCh37 chr3: 195,419,168-197,387,258 , GRCh38.p12 chr3: 195,692,297-197,660,387 NCBP2AS2, DLG1-AS1, 67 more genes
    nsv5200362copy number variation1nstd102humanPathogenic GRCh37 chr3: 195,747,856-197,387,258 , GRCh38.p12 chr3: 196,020,985-197,660,387 MIR4797, SDHAP4, 52 more genes
    nsv5095448mobile element insertion1nstd203human GRCh38 chr3: 196,471,196-196,471,229 , GRCh37.p13 chr3: 196,198,067-196,198,100 RNF168
    nsv5095321mobile element insertion1nstd203human GRCh38 chr3: 196,471,147-196,471,196 , GRCh37.p13 chr3: 196,198,018-196,198,067 RNF168
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