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Items: 1 to 20 of 214

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6917370copy number variation1nstd229human GRCh38 chr11: 4,555,024-4,581,193 , GRCh37.p13 chr11: 4,576,254-4,602,423 C11orf40
    nsv6917011copy number variation1nstd229human GRCh38 chr11: 2,693,282-9,207,515 , GRCh37.p13 chr11: 2,714,512-9,229,062 LOC105376526, OR51E2, 279 more genes
    nsv6916316copy number variation1nstd229human GRCh38 chr11: 4,495,101-4,614,600 , GRCh37.p13 chr11: 4,516,331-4,635,830 OR52M2P, OR52I2, 4 more genes
    nsv6916237copy number variation1nstd229human GRCh38 chr11: 4,369,424-4,697,710 , GRCh37.p13 chr11: 4,390,654-4,718,940 TRIM68, OR51E2, 17 more genes
    nsv6916129copy number variation1nstd229human GRCh38 chr11: 3,833,721-4,728,036 , GRCh37.p13 chr11: 3,854,951-4,749,266 OR52K1, OR52B4, 39 more genes
    nsv6914951copy number variation1nstd229human GRCh38 chr11: 4,515,180-4,719,642 , GRCh37.p13 chr11: 4,536,410-4,740,872 OR51A9P, OR52M1, 12 more genes
    nsv6914790copy number variation1nstd229human GRCh38 chr11: 4,568,229-4,572,360 , GRCh37.p13 chr11: 4,589,459-4,593,590 C11orf40
    nsv6913480copy number variation1nstd229human GRCh38 chr11: 4,561,801-4,571,700 , GRCh37.p13 chr11: 4,583,031-4,592,930 C11orf40
    nsv6910853copy number variation1nstd229human GRCh38 chr11: 4,496,473-4,621,051 , GRCh37.p13 chr11: 4,517,703-4,642,281 C11orf40, OR52I1, 4 more genes
    nsv6907396copy number variation1nstd229human GRCh38 chr11: 4,560,919-4,669,992 , GRCh37.p13 chr11: 4,582,149-4,691,222 TRIM68, OR52I2, 6 more genes
    nsv6906415copy number variation1nstd229human GRCh38 chr11: 4,556,809-4,577,728 , GRCh37.p13 chr11: 4,578,039-4,598,958 C11orf40
    nsv6903543copy number variation1nstd229human GRCh38 chr11: 4,563,990-4,571,533 , GRCh37.p13 chr11: 4,585,220-4,592,763 C11orf40
    nsv6902905copy number variation1nstd229human GRCh38 chr11: 4,568,821-4,590,188 , GRCh37.p13 chr11: 4,590,051-4,611,418 OR52I2, C11orf40
    nsv6900520copy number variation1nstd229human GRCh38 chr11: 4,562,140-4,616,444 , GRCh37.p13 chr11: 4,583,370-4,637,674 TRIM68, C11orf40, 2 more genes
    nsv6899889copy number variation1nstd229human GRCh38 chr11: 4,547,595-4,575,144 , GRCh37.p13 chr11: 4,568,825-4,596,374 C11orf40
    nsv6898802copy number variation1nstd229human GRCh38 chr11: 4,560,087-4,573,134 , GRCh37.p13 chr11: 4,581,317-4,594,364 C11orf40
    nsv6638006copy number variation1nstd102humanUncertain significance GRCh37 chr11: 4,384,773-4,681,230 , GRCh38.p12 chr11: 4,363,543-4,660,000 OR51R1P, OR52I1, 15 more genes
    nsv6637864copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177 PNPLA2, OR52H1, 372 more genes
    nsv6634327copy number variation1nstd102humanPathogenic GRCh38 chr11: 499,700-5,279,697 , GRCh37.p13 chr11: 499,700-5,300,927 SNORA54, PIDD1, 219 more genes
    nsv6454095copy number variation1nstd223human GRCh38 chr11: 4,571,523-4,572,519 , GRCh37.p13 chr11: 4,592,753-4,593,749 C11orf40
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