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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6908880copy number variation1nstd229human GRCh38 chr11: 58,189,925-58,194,324 , GRCh37.p13 chr11: 57,957,397-57,961,796 OR9Q2
    nsv5923472copy number variation1nstd209human GRCh38 chr11: 58,188,406-58,193,597 , GRCh37.p13 chr11: 57,955,878-57,961,069 OR9Q2
    nsv4979531copy number variation1nstd200human GRCh38 chr11: 58,189,925-58,194,321 , GRCh37.p13 chr11: 57,957,397-57,961,793 OR9Q2
    nsv4837771copy number variation1nstd200human GRCh37 chr11: 57,957,397-57,961,793 , GRCh38.p12 chr11: 58,189,925-58,194,321 OR9Q2
    nsv4846024copy number variation1nstd200human GRCh37 chr11: 57,956,611-57,957,056 , GRCh38.p12 chr11: 58,189,139-58,189,584 OR9Q2
    nsv4196259copy number variation1nstd166human GRCh37.p13 chr11: 57,956,611-57,957,056 , GRCh38.p12 chr11: 58,189,139-58,189,584 OR9Q2
    nsv5852393copy number variation1nstd209human GRCh38 chr11: 58,188,313-58,193,660 , GRCh37.p13 chr11: 57,955,785-57,961,132 OR9Q2
    nsv7070535inversion1nstd229human GRCh38 chr11: 58,190,653-58,190,841 , GRCh37.p13 chr11: 57,958,125-57,958,313 OR9Q2
    esv3768364complex chromosomal rearrangement1estd192human GRCh37 chr8: 48,726,299-48,726,299 , GRCh37 chr11: 57,956,836-57,956,836 , GRCh38.p12 chr11: 58,189,364-58,189,364 , GRCh38.p12 chr8: 47,813,738-47,813,738 OR9Q2, PRKDC
    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
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 LOC105376598, OSBPL9P2, 2842 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 RTN3, KRTAP5-13P, 2833 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
    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
    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
    nsv3904152copy number variation1nstd102humanUncertain significance GRCh37 chr11: 49,313,405-59,008,426 , GRCh38.p12 chr11: 49,291,853-59,240,953 FAM111B, OR5M1, 250 more genes
    nsv984845copy number variation3nstd11human NCBI36 chr11: 188,510-134,449,982 , GRCh37.p13 chr11: 198,510-134,944,770 , GRCh38.p12 chr11: 198,510-135,074,876 , ACAT1, 2903 more genes
    nsv429597copy number variation1nstd11human NCBI36 chr11: 50,952,568-134,449,982 , GRCh37.p13 chr11: 51,095,992-134,944,770 , GRCh38.p12 chr11: 54,926,733-135,074,876 , ACAT1, 1883 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
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