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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094710copy number variation1nstd102humanPathogenic GRCh37 chr15: 44,941,044-44,944,484 , GRCh38.p12 chr15: 44,648,846-44,652,286 SPG11
    nsv7094709copy number variation1nstd102humanPathogenic GRCh37 chr15: 44,855,319-44,952,834 , GRCh38.p12 chr15: 44,563,121-44,660,636 EIF3J, SPG11
    nsv7094537copy number variation1nstd102humanPathogenic GRCh37 chr15: 44,912,368-44,925,855 , GRCh38.p12 chr15: 44,620,170-44,633,657 SPG11
    nsv7094536copy number variation1nstd102humanUncertain significance GRCh37 chr15: 44,855,319-44,878,413 , GRCh38.p12 chr15: 44,563,121-44,586,215 EIF3J, SPG11
    nsv7094374copy number variation1nstd102humanPathogenic GRCh37 chr15: 44,884,509-44,884,656 , GRCh38.p12 chr15: 44,592,311-44,592,458 SPG11
    nsv7094292copy number variation1nstd102humanUncertain significance GRCh37 chr15: 44,877,814-44,955,845 , GRCh38.p12 chr15: 44,585,616-44,663,647 SPG11
    nsv7094291copy number variation1nstd102humanPathogenic GRCh37 chr15: 44,877,814-44,878,413 , GRCh38.p12 chr15: 44,585,616-44,586,215 SPG11
    nsv7093617insertion1nstd102humanPathogenic GRCh37 chr15: 44,864,897-44,864,897 , GRCh38 chr15: 44,572,699-44,572,699 SPG11
    nsv7093494delins1nstd102humanPathogenic GRCh37 chr15: 44,887,634-44,887,639 , GRCh38 chr15: 44,595,436-44,595,441 SPG11
    nsv6314291insertion1nstd102humanUncertain significance GRCh38 chr15: 44,652,109-44,652,109 , GRCh37 chr15: 44,944,307-44,944,307 SPG11
    nsv6309790copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 44,887,437-44,891,054 , GRCh38.p12 chr15: 44,595,239-44,598,856 SPG11
    nsv6309623copy number variation1nstd102humanPathogenic GRCh37 chr15: 44,898,203-44,907,784 , GRCh38.p12 chr15: 44,606,005-44,615,586 SPG11
    nsv6309622copy number variation1nstd102humanPathogenic GRCh37 chr15: 44,888,261-44,892,850 , GRCh38.p12 chr15: 44,596,063-44,600,652 SPG11
    nsv6309621copy number variation1nstd102humanPathogenic GRCh37 chr15: 44,887,437-44,892,850 , GRCh38.p12 chr15: 44,595,239-44,600,652 SPG11
    nsv6309620copy number variation1nstd102humanUncertain significance GRCh37 chr15: 44,877,814-44,881,632 , GRCh38.p12 chr15: 44,585,616-44,589,434 SPG11
    nsv6309619copy number variation1nstd102humanPathogenic GRCh37 chr15: 44,864,989-44,988,554 , GRCh38.p12 chr15: 44,572,791-44,696,356 SPG11, PATL2
    nsv6309618copy number variation1nstd102humanUncertain significance GRCh37 chr15: 44,855,319-44,867,259 , GRCh38.p12 chr15: 44,563,121-44,575,061 EIF3J, SPG11
    nsv6309581copy number variation1nstd102humanPathogenic GRCh37 chr15: 44,890,443-44,890,591 , GRCh38.p12 chr15: 44,598,245-44,598,393 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
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