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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5943269copy number variation1nstd209human GRCh38 chr15: 44,654,749-44,654,808 , GRCh37.p13 chr15: 44,946,947-44,947,006 SPG11
    nsv5674311insertion1nstd102humanPathogenic GRCh37 chr15: 44,925,783-44,925,783 , GRCh38 chr15: 44,633,585-44,633,585 SPG11
    nsv5672824copy number variation1nstd102humanPathogenic GRCh37 chr15: 44,918,519-44,921,596 , GRCh38.p12 chr15: 44,626,321-44,629,398 SPG11
    nsv5672822copy number variation1nstd102humanPathogenic GRCh37 chr15: 44,881,444-44,925,841 , GRCh38.p12 chr15: 44,589,246-44,633,643 SPG11
    nsv5672821copy number variation1nstd102humanPathogenic GRCh37 chr15: 44,862,703-44,862,876 , GRCh38.p12 chr15: 44,570,505-44,570,678 SPG11
    nsv5672741copy number variation1nstd102humanPathogenic GRCh37 chr15: 44,941,054-44,944,474 , GRCh38.p12 chr15: 44,648,856-44,652,276 SPG11
    nsv5672740copy number variation1nstd102humanPathogenic GRCh37 chr15: 44,862,713-44,867,249 , GRCh38.p12 chr15: 44,570,515-44,575,051 SPG11
    nsv5672666copy number variation1nstd102humanPathogenic GRCh37 chr15: 44,876,002-44,876,766 , GRCh38.p12 chr15: 44,583,804-44,584,568 SPG11
    nsv5672661copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 44,925,748-44,925,860 , GRCh38 chr15: 44,633,550-44,633,662 SPG11
    nsv5654748insertion1nstd207human GRCh38 chr15: 44,616,782-44,616,782 , GRCh37.p13 chr15: 44,908,980-44,908,980 SPG11
    nsv5531650copy number variation1nstd206human GRCh38 chr15: 44,654,751-44,654,809 , GRCh37.p13 chr15: 44,946,949-44,947,007 SPG11
    nsv5514949copy number variation1nstd206human GRCh38 chr15: 44,610,049-44,610,508 , GRCh37.p13 chr15: 44,902,247-44,902,706 SPG11
    nsv5380762copy number variation1nstd102humanUncertain significance GRCh37 chr15: 44,855,319-45,898,712 , GRCh38.p12 chr15: 44,563,121-45,606,514 LOC100533853, RNU6-1108P, 44 more genes
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5186413mobile element insertion1nstd203human GRCh38 chr15: 44,568,390-44,568,398 , GRCh37.p13 chr15: 44,860,588-44,860,596 SPG11
    nsv5181089mobile element insertion1nstd203human GRCh38 chr15: 44,588,502-44,588,502 , GRCh37.p13 chr15: 44,880,700-44,880,700 SPG11
    nsv5158606mobile element insertion1nstd203human GRCh38 chr15: 44,576,120-44,576,142 , GRCh37.p13 chr15: 44,868,318-44,868,340 SPG11
    nsv5157684mobile element insertion1nstd203human GRCh38 chr15: 44,636,925-44,636,968 , GRCh37.p13 chr15: 44,929,123-44,929,166 SPG11
    nsv5155603mobile element insertion1nstd203human GRCh38 chr15: 44,588,502-44,588,515 , GRCh37.p13 chr15: 44,880,700-44,880,713 SPG11
    nsv5153763mobile element insertion1nstd203human GRCh38 chr15: 44,609,102-44,609,113 , GRCh37.p13 chr15: 44,901,300-44,901,311 SPG11
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