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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098459copy number variation1nstd102humanUncertain significance GRCh37 chr9: 35,546,519-35,561,379 , GRCh38.p12 chr9: 35,546,522-35,561,382 CIMIP2B, RUSC2
    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
    nsv7063189inversion1nstd229human GRCh38 chr9: 35,556,949-35,557,053 , GRCh37.p13 chr9: 35,556,946-35,557,050 RUSC2
    nsv7061879inversion1nstd229human GRCh38 chr9: 35,537,344-35,542,082 , GRCh37.p13 chr9: 35,537,341-35,542,079 RUSC2
    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
    nsv6875496copy number variation1nstd229human GRCh38 chr9: 35,550,141-35,550,558 , GRCh37.p13 chr9: 35,550,138-35,550,555 RUSC2
    nsv6874687copy number variation1nstd229human GRCh38 chr9: 35,554,056-35,554,283 , GRCh37.p13 chr9: 35,554,053-35,554,280 RUSC2
    nsv6873962copy number variation1nstd229human GRCh38 chr9: 35,494,162-35,499,311 , GRCh37.p13 chr9: 35,494,159-35,499,308 RUSC2
    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
    nsv6871393copy number variation1nstd229human GRCh38 chr9: 35,494,201-35,501,600 , GRCh37.p13 chr9: 35,494,198-35,501,597 RUSC2
    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
    nsv6869694copy number variation1nstd229human GRCh38 chr9: 35,561,379-35,564,109 , GRCh37.p13 chr9: 35,561,376-35,564,106 CIMIP2B, RUSC2
    nsv6869004copy number variation1nstd229human GRCh38 chr9: 35,529,901-35,865,200 , GRCh37.p13 chr9: 35,529,898-35,865,197 TESK1, MIR4667, 25 more genes
    nsv6868904copy number variation1nstd229human GRCh38 chr9: 35,528,202-35,532,009 , GRCh37.p13 chr9: 35,528,199-35,532,006 RUSC2
    nsv6866328copy number variation1nstd229human GRCh38 chr9: 35,493,081-35,504,387 , GRCh37.p13 chr9: 35,493,078-35,504,384 RUSC2, LOC105376026
    nsv6864637copy number variation1nstd229human GRCh38 chr9: 35,524,354-35,528,629 , GRCh37.p13 chr9: 35,524,351-35,528,626 RUSC2
    nsv6862579copy number variation1nstd229human GRCh38 chr9: 35,546,901-35,914,300 , GRCh37.p13 chr9: 35,546,898-35,914,297 RPS29P17, CCDC107, 29 more genes
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