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Items: 1 to 20 of 118

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093770copy number variation1nstd102humanUncertain significance GRCh37 chr11: 59,939,307-60,235,941 , GRCh38.p12 chr11: 60,171,834-60,468,468 MS4A5, MS4A4E, 7 more genes
    nsv7093694copy number variation2nstd102humanUncertain significance GRCh37 chr11: 58,916,346-64,972,349 , GRCh38.p12 chr11: 59,148,873-65,204,878 VPS37C, POLR2G, 298 more genes
    nsv7076174inversion1nstd229human GRCh38 chr11: 57,437,573-64,138,990 , GRCh37.p13 chr11: 57,205,046-63,906,462 RNU2-2P, SLC43A1, 299 more genes
    nsv6913935copy number variation1nstd229human GRCh38 chr11: 60,283,291-60,459,015 , GRCh37.p13 chr11: 60,050,764-60,226,488 MS4A7, MS4A5, 4 more genes
    nsv6908366copy number variation1nstd229human GRCh38 chr11: 60,121,080-60,521,495 , GRCh37.p13 chr11: 59,888,553-60,288,968 MS4A5, MS4A4E, 10 more genes
    nsv6903095copy number variation1nstd229human GRCh38 chr11: 59,466,654-66,168,743 , GRCh37.p13 chr11: 59,234,127-65,936,214 LINC02724, TMEM132A, 342 more genes
    nsv6900171copy number variation1nstd229human GRCh38 chr11: 60,329,947-60,330,493 , GRCh37.p13 chr11: 60,097,420-60,097,966 MS4A6E
    nsv6899702copy number variation1nstd229human GRCh38 chr11: 60,339,494-60,344,566 , GRCh37.p13 chr11: 60,106,967-60,112,039 MS4A6E
    nsv6898635copy number variation1nstd229human GRCh38 chr11: 60,327,178-60,332,161 , GRCh37.p13 chr11: 60,094,651-60,099,634 MS4A6E
    nsv6462074copy number variation1nstd223human GRCh38 chr11: 60,329,949-60,330,467 , GRCh37.p13 chr11: 60,097,422-60,097,940 MS4A6E
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6315474copy number variation1nstd102humanPathogenic GRCh37 chr11: 43,607,886-61,466,671 , GRCh38.p12 chr11: 43,586,336-61,699,199 TRR-TCT3-2, OR4A41P, 494 more genes
    nsv6121130copy number variation1nstd186human GRCh37 chr11: 60,097,442-60,097,937 , GRCh38.p12 chr11: 60,329,969-60,330,464 MS4A6E
    nsv6035153copy number variation1nstd212human GRCh38 chr11: 60,329,929-60,330,445 , GRCh37.p13 chr11: 60,097,402-60,097,918 MS4A6E
    nsv5918803copy number variation1nstd209human GRCh38 chr11: 60,329,963-60,330,477 , GRCh37.p13 chr11: 60,097,436-60,097,950 MS4A6E
    nsv5593347copy number variation1nstd207human GRCh38 chr11: 60,329,929-60,330,444 , GRCh37.p13 chr11: 60,097,402-60,097,917 MS4A6E
    nsv5508250copy number variation1nstd206human GRCh38 chr11: 60,329,969-60,330,464 , GRCh37.p13 chr11: 60,097,442-60,097,937 MS4A6E
    nsv5493940copy number variation1nstd206human GRCh38 chr11: 60,335,057-60,335,139 , GRCh37.p13 chr11: 60,102,530-60,102,612 MS4A6E
    nsv5392958copy number variation1nstd186human GRCh37 chr11: 60,097,431-60,097,918 , GRCh38.p12 chr11: 60,329,958-60,330,445 MS4A6E
    nsv5392950copy number variation1nstd186human GRCh37 chr11: 60,097,442-60,097,917 , GRCh38.p12 chr11: 60,329,969-60,330,444 MS4A6E
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