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Items: 1 to 20 of 72

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076174inversion1nstd229human GRCh38 chr11: 57,437,573-64,138,990 , GRCh37.p13 chr11: 57,205,046-63,906,462 RNU2-2P, SLC43A1, 299 more genes
    nsv7070535inversion1nstd229human GRCh38 chr11: 58,190,653-58,190,841 , GRCh37.p13 chr11: 57,958,125-57,958,313 OR9Q2
    nsv7068318inversion1nstd229human GRCh38 chr11: 58,150,576-58,242,317 , GRCh37.p13 chr11: 57,918,048-58,009,789 OR5BL1P, OR9Q2, 5 more genes
    nsv6908880copy number variation1nstd229human GRCh38 chr11: 58,189,925-58,194,324 , GRCh37.p13 chr11: 57,957,397-57,961,796 OR9Q2
    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
    nsv6101017inversion1nstd212human GRCh38 chr11: 54,578,670-59,501,927 , GRCh37.p13 chr11: 54,711,406-59,269,400 , APLNR, 236 more genes
    nsv5978690inversion1nstd209human GRCh38 chr11: 58,000,184-58,217,938 , GRCh37.p13 chr11: 57,767,656-57,985,410 OR9L1P, OR9I3P, 13 more genes
    nsv5923472copy number variation1nstd209human GRCh38 chr11: 58,188,406-58,193,597 , GRCh37.p13 chr11: 57,955,878-57,961,069 OR9Q2
    nsv5852393copy number variation1nstd209human GRCh38 chr11: 58,188,313-58,193,660 , GRCh37.p13 chr11: 57,955,785-57,961,132 OR9Q2
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv4979531copy number variation1nstd200human GRCh38 chr11: 58,189,925-58,194,321 , GRCh37.p13 chr11: 57,957,397-57,961,793 OR9Q2
    nsv4846024copy number variation1nstd200human GRCh37 chr11: 57,956,611-57,957,056 , GRCh38.p12 chr11: 58,189,139-58,189,584 OR9Q2
    nsv4837771copy number variation1nstd200human GRCh37 chr11: 57,957,397-57,961,793 , GRCh38.p12 chr11: 58,189,925-58,194,321 OR9Q2
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4334316sequence alteration1nstd166human GRCh37.p13 chr11: 57,918,047-58,133,767 , GRCh38.p12 chr11: 58,150,575-58,366,294 OR9Q2, OR10Q1, 13 more genes
    nsv4196259copy number variation1nstd166human GRCh37.p13 chr11: 57,956,611-57,957,056 , GRCh38.p12 chr11: 58,189,139-58,189,584 OR9Q2
    nsv3911150copy number variation1nstd102humanPathogenic GRCh37 chr11: 55,086,995-58,766,250 , NCBI36 chr11: 54,843,571-58,522,826 , GRCh38 chr11: 55,319,519-58,998,777 OR5BD1P, SELENOH, 197 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
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