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Items: 1 to 20 of 233

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6910871copy number variation1nstd229human GRCh38 chr11: 5,875,715-5,918,513 , GRCh37.p13 chr11: 5,896,945-5,939,743 LOC112268071, OR52E4, 2 more genes
    nsv6910553copy number variation1nstd229human GRCh38 chr11: 5,903,814-5,910,382 , GRCh37.p13 chr11: 5,925,044-5,931,612 LOC112268071, OR52Q1P
    nsv6902633copy number variation1nstd229human GRCh38 chr11: 5,538,086-5,938,396 , GRCh37.p13 chr11: 5,559,316-5,959,626 OR52N1, OR52N4, 26 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
    nsv6621254copy number variation30nstd224human GRCh37 chr11: 5,886,773-5,933,445 , GRCh38.p12 chr11: 5,865,543-5,912,215 OR52Q1P, OR52E5, 3 more genes
    nsv6621251copy number variation1nstd224human GRCh37 chr11: 5,727,822-5,995,159 , GRCh38.p12 chr11: 5,706,592-5,973,929 TRIM22, OR52N1, 17 more genes
    nsv6621191copy number variation2nstd224human GRCh37 chr11: 5,882,168-5,933,445 , GRCh38.p12 chr11: 5,860,938-5,912,215 OR52E7P, OR52E4, 3 more genes
    nsv6621122copy number variation1nstd224human GRCh37 chr11: 5,920,721-5,989,293 , GRCh38.p12 chr11: 5,899,491-5,968,063 OR52E5, LOC112268071, 3 more genes
    nsv6621117copy number variation6nstd224human GRCh37 chr11: 5,895,754-5,933,445 , GRCh38.p12 chr11: 5,874,524-5,912,215 LOC112268071, OR52E5, 3 more genes
    nsv6621006copy number variation3nstd224human GRCh37 chr11: 5,905,639-5,923,082 , GRCh38.p12 chr11: 5,884,409-5,901,852 OR52E4, OR52E5, 2 more genes
    nsv6621005copy number variation15nstd224human GRCh37 chr11: 5,905,557-5,923,082 , GRCh38.p12 chr11: 5,884,327-5,901,852 OR52Q1P, OR52E4, 2 more genes
    nsv6591706inversion1nstd223human GRCh38 chr11: 5,868,029-5,920,669 , GRCh37.p13 chr11: 5,889,259-5,941,899 OR52Q1P, OR52E7P, 3 more genes
    nsv6444268copy number variation1nstd223human GRCh38 chr11: 5,862,301-5,928,000 , GRCh37.p13 chr11: 5,883,531-5,949,230 OR52E4, OR52Q1P, 3 more genes
    nsv6441849copy number variation1nstd223human GRCh38 chr11: 5,588,812-6,011,442 , GRCh37.p13 chr11: 5,610,042-6,032,672 OR52N5, OR52N4, 26 more genes
    nsv6437487copy number variation1nstd223human GRCh38 chr11: 5,568,264-6,075,481 , GRCh37.p13 chr11: 5,589,494-6,096,711 TRIM34, OR52E6, 33 more genes
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6121247copy number variation1nstd186human GRCh37 chr11: 5,883,955-5,936,300 , GRCh38.p12 chr11: 5,862,725-5,915,070 OR52Q1P, OR52E7P, 3 more genes
    nsv6033696copy number variation1nstd212human GRCh38 chr11: 5,862,721-5,915,403 , GRCh37.p13 chr11: 5,883,951-5,936,633 OR52Q1P, OR52E7P, 3 more genes
    nsv5910194copy number variation1nstd209human GRCh38 chr11: 5,862,725-5,915,396 , GRCh37.p13 chr11: 5,883,955-5,936,626 OR52E7P, OR52E4, 3 more genes
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