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Items: 1 to 20 of 268

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098455copy number variation6nstd102humanUncertain significance GRCh37 chr9: 32,453,279-37,785,041 , GRCh38.p12 chr9: 32,453,281-37,785,044 TRBVAOR9-2, UBAP2, 197 more genes
    nsv7098082copy number variation1nstd102humanUncertain significance GRCh37 chr9: 34,370,797-36,276,941 , GRCh38.p12 chr9: 34,370,799-36,276,944 UNC13B, CD72, 86 more genes
    nsv7067764inversion1nstd229human GRCh38 chr9: 35,429,231-35,436,897 , GRCh37.p13 chr9: 35,429,228-35,436,894 ATP8B5P
    nsv7066996inversion1nstd229human GRCh38 chr9: 35,240,127-35,414,862 , GRCh37.p13 chr9: 35,240,124-35,414,859 UNC13B, ATP8B5P
    nsv7060547inversion1nstd229human GRCh38 chr9: 35,282,974-35,527,178 , GRCh37.p13 chr9: 35,282,971-35,527,175 RUSC2, LOC105376026, 4 more genes
    nsv7060440inversion1nstd229human GRCh38 chr9: 33,533,890-38,610,880 , GRCh37.p13 chr9: 33,533,888-38,610,877 FRMPD1, PTENP1, 182 more genes
    nsv7058978inversion1nstd229human GRCh38 chr9: 33,570,636-38,550,207 , GRCh37.p13 chr9: 33,570,634-38,550,204 TRBV29OR9-2, SPMIP6, 180 more genes
    nsv7058100inversion1nstd229human GRCh38 chr9: 35,428,924-35,441,841 , GRCh37.p13 chr9: 35,428,921-35,441,838 ATP8B5P
    nsv6877546copy number variation1nstd229human GRCh38 chr9: 35,161,160-35,408,187 , GRCh37.p13 chr9: 35,161,157-35,408,184 UNC13B, ATP8B5P
    nsv6873728copy number variation1nstd229human GRCh38 chr9: 35,473,399-35,515,837 , GRCh37.p13 chr9: 35,473,396-35,515,834 RPL36AP33, RUSC2, 2 more genes
    nsv6870782copy number variation1nstd229human GRCh38 chr9: 35,433,323-35,445,549 , GRCh37.p13 chr9: 35,433,320-35,445,546 ATP8B5P
    nsv6870133copy number variation1nstd229human GRCh38 chr9: 34,043,094-35,876,103 , GRCh37.p13 chr9: 34,043,092-35,876,100 STOML2, ENHO, 85 more genes
    nsv6866720copy number variation1nstd229human GRCh38 chr9: 35,457,976-35,460,840 , GRCh37.p13 chr9: 35,457,973-35,460,837 ATP8B5P
    nsv6859179copy number variation1nstd229human GRCh38 chr9: 35,463,000-35,464,672 , GRCh37.p13 chr9: 35,462,997-35,464,669 ATP8B5P
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6634409copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 1-40,036,525 , GRCh38.p12 chr9: 10,001-39,445,729 ACO1, PLIN2, 594 more genes
    nsv6560363inversion1nstd223human GRCh38 chr9: 33,533,993-38,610,852 , GRCh37.p13 chr9: 33,533,991-38,610,849 PHF24, CNTFR, 182 more genes
    nsv6556213inversion1nstd223human GRCh38 chr9: 35,454,914-35,459,109 , GRCh37.p13 chr9: 35,454,911-35,459,106 ATP8B5P
    nsv6454768copy number variation1nstd223human GRCh38 chr9: 35,425,147-35,428,977 , GRCh37.p13 chr9: 35,425,144-35,428,974 ATP8B5P
    nsv6448553copy number variation1nstd223human GRCh38 chr9: 35,415,956-35,418,080 , GRCh37.p13 chr9: 35,415,953-35,418,077 ATP8B5P
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