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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv4978410copy number variation1nstd200human GRCh38 chr11: 17,073,792-17,073,901 , GRCh37.p13 chr11: 17,095,339-17,095,448 RPS13, SNORD14B, 1 more genes
    nsv4978406copy number variation1nstd200human GRCh38 chr11: 17,036,947-17,073,915 , GRCh37.p13 chr11: 17,058,494-17,095,462 SNORD14A, OR7E14P, 2 more genes
    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
    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
    nsv4602717copy number variation1nstd183human GRCh37 chr11: 16,913,860-18,038,721 , GRCh38.p12 chr11: 16,892,313-18,017,174 , LINC02729, 27 more genes
    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
    nsv4456294copy number variation1nstd102humanUncertain significance GRCh37 chr11: 16,914,628-17,201,011 , GRCh38.p12 chr11: 16,893,081-17,179,464 RPL36AP37, PIK3C2A, 8 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
    nsv4455131copy number variation2nstd102humanUncertain significance, Likely benign GRCh37 chr11: 16,914,628-17,199,531 , GRCh38.p12 chr11: 16,893,081-17,177,984 SNORD147, PLEKHA7, 8 more genes
    nsv4207042copy number variation1nstd166human GRCh37.p13 chr11: 17,048,030-17,472,217 , GRCh38.p12 chr11: 17,026,483-17,450,670 , OR7E14P, 15 more genes
    nsv4195431copy number variation1nstd166human GRCh37.p13 chr11: 17,095,339-17,095,448 , GRCh38.p12 chr11: 17,073,792-17,073,901 RPS13, SNORD14B, 1 more genes
    nsv3912558copy number variation1nstd102humanPathogenic GRCh37 chr11: 446,754-18,926,289 , GRCh38 chr11: 446,754-18,904,742 , NCBI36 chr11: 436,754-18,882,865 TRIM22, CSNK2A3, 546 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
    nsv3906221copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-31,995,219 , GRCh38.p12 chr11: 230,615-31,973,673 PCNAP4, LIN7C, 688 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
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