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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5727630mobile element insertion2nstd211human GRCh38 chr11: 17,755,379-17,755,379 , GRCh37.p13 chr11: 17,776,926-17,776,926 KCNC1
    nsv5511421copy number variation1nstd206human GRCh38 chr11: 17,732,933-17,734,263 , GRCh37.p13 chr11: 17,754,480-17,755,810 KCNC1
    nsv5507673copy number variation1nstd206human GRCh38 chr11: 16,359,999-20,627,000 , GRCh37.p13 chr11: 16,381,545-20,648,546 , CSRP3, 102 more genes
    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
    nsv5380720copy number variation1nstd102humanUncertain significance GRCh37 chr11: 17,552,691-19,213,995 , GRCh38.p12 chr11: 17,531,144-19,192,448 USH1C, HIGD1AP5, 53 more genes
    nsv4978436copy number variation1nstd200human GRCh38 chr11: 17,746,208-17,747,153 , GRCh37.p13 chr11: 17,767,755-17,768,700 KCNC1
    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
    nsv4729618copy number variation1nstd102humanUncertain significance GRCh37 chr11: 17,461,542-17,773,192 , GRCh38.p12 chr11: 17,439,995-17,751,645 ABCC8, MYOD1, 4 more genes
    nsv4682956copy number variation1nstd102humanUncertain significance GRCh37 chr11: 17,757,530-17,803,301 , GRCh38.p12 chr11: 17,735,983-17,781,754 KCNC1
    nsv4675502copy number variation1nstd102humanPathogenic GRCh37 chr11: 13,970,757-27,565,888 , GRCh38.p12 chr11: 13,949,210-27,544,341 MRGPRX5P, LDHC, 171 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4674824copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,053,978-34,732,891 , GRCh38.p12 chr11: 11,032,431-34,711,344 SNORA88, LINC02729, 305 more genes
    nsv4641043copy number variation1nstd186human GRCh37 chr11: 17,754,466-17,755,810 , GRCh38.p12 chr11: 17,732,919-17,734,263 KCNC1
    nsv4602717copy number variation1nstd183human GRCh37 chr11: 16,913,860-18,038,721 , GRCh38.p12 chr11: 16,892,313-18,017,174 , LINC02729, 27 more genes
    nsv4538438insertion1nstd166human GRCh37.p13 chr11: 17,754,433-17,754,433 , GRCh38.p12 chr11: 17,732,886-17,732,886 KCNC1
    nsv4456716copy number variation1nstd102humanUncertain significance GRCh37 chr11: 16,775,884-18,418,719 , GRCh38.p12 chr11: 16,754,337-18,397,172 RNU6-593P, SNORD14A, 47 more genes
    nsv4455290copy number variation1nstd102humanUncertain significance GRCh37 chr11: 16,436,272-18,064,677 , GRCh38.p12 chr11: 16,414,726-18,043,130 LOC105376571, PIK3C2A, 30 more genes
    nsv4414428copy number variation1nstd174human GRCh37 chr11: 17,723,530-17,794,577 , GRCh38.p12 chr11: 17,701,983-17,773,030 KCNC1, MYOD1
    nsv4208849copy number variation1nstd166human GRCh37.p13 chr11: 17,779,048-17,779,267 , GRCh38.p12 chr11: 17,757,501-17,757,720 KCNC1
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