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Items: 1 to 20 of 147

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098477copy number variation1nstd102humanPathogenic GRCh37 chr9: 94,485,944-95,527,026 , GRCh38.p12 chr9: 91,723,662-92,764,744 LINC00475, MTATP6P29, 30 more genes
    nsv7071376inversion1nstd229human GRCh38 chr9: 92,156,858-92,156,981 , GRCh37.p13 chr9: 94,919,140-94,919,263 LINC00475
    nsv7069070inversion1nstd229human GRCh38 chr9: 92,131,674-92,197,847 , GRCh37.p13 chr9: 94,893,956-94,960,129 BEND3P2, LOC100128076, 2 more genes
    nsv7064397inversion1nstd229human GRCh38 chr9: 92,138,949-92,150,307 , GRCh37.p13 chr9: 94,901,231-94,912,589 LOC100128076, LINC00475
    nsv7063061inversion1nstd229human GRCh38 chr9: 92,128,952-92,200,598 , GRCh37.p13 chr9: 94,891,234-94,962,880 LOC100128076, BEND3P2, 2 more genes
    nsv6875073copy number variation1nstd229human GRCh38 chr9: 92,156,003-92,156,205 , GRCh37.p13 chr9: 94,918,285-94,918,487 LINC00475
    nsv6874970copy number variation1nstd229human GRCh38 chr9: 91,869,996-92,164,079 , GRCh37.p13 chr9: 94,632,278-94,926,361 LOC107987094, ROR2, 11 more genes
    nsv6871191copy number variation1nstd229human GRCh38 chr9: 92,144,811-92,148,321 , GRCh37.p13 chr9: 94,907,093-94,910,603 LINC00475
    nsv6870487copy number variation1nstd229human GRCh38 chr9: 91,906,361-92,583,443 , GRCh37.p13 chr9: 94,668,643-95,345,725 ROR2, LOC100420779, 25 more genes
    nsv6866880copy number variation1nstd229human GRCh38 chr9: 92,135,926-92,160,911 , GRCh37.p13 chr9: 94,898,208-94,923,193 LOC100128076, LINC00475
    nsv6866039copy number variation1nstd229human GRCh38 chr9: 92,147,199-92,147,267 , GRCh37.p13 chr9: 94,909,481-94,909,549 LINC00475
    nsv6863870copy number variation1nstd229human GRCh38 chr9: 92,097,159-92,249,257 , GRCh37.p13 chr9: 94,859,441-95,011,539 LOC112268048, LOC100420896, 10 more genes
    nsv6863807copy number variation1nstd229human GRCh38 chr9: 92,159,802-92,159,861 , GRCh37.p13 chr9: 94,922,084-94,922,143 LINC00475
    nsv6861344copy number variation1nstd229human GRCh38 chr9: 92,159,499-92,166,366 , GRCh37.p13 chr9: 94,921,781-94,928,648 LINC00475
    nsv6860652copy number variation1nstd229human GRCh38 chr9: 91,924,473-92,376,273 , GRCh37.p13 chr9: 94,686,755-95,138,555 LOC100420896, RPL21P82, 20 more genes
    nsv6637685copy number variation1nstd102humanUncertain significance GRCh37 chr9: 94,666,958-95,339,157 , GRCh38.p12 chr9: 91,904,676-92,576,875 ECM2, IARS1, 25 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
    nsv6556848inversion1nstd223human GRCh38 chr9: 90,743,255-92,932,434 , GRCh37.p13 chr9: 93,505,537-95,694,716 MIR3651, IARS1, 54 more genes
    nsv6449163copy number variation1nstd223human GRCh38 chr9: 91,869,996-92,164,079 , GRCh37.p13 chr9: 94,632,278-94,926,361 HSPE1P22, LOC100128076, 11 more genes
    nsv6445900copy number variation1nstd223human GRCh38 chr9: 92,130,653-92,139,500 , GRCh37.p13 chr9: 94,892,935-94,901,782 LOC100128076, LINC00475
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