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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
    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
    nsv4984240copy number variation1nstd200human GRCh38 chr11: 18,366,168-18,410,341 , GRCh37.p13 chr11: 18,387,715-18,431,888 LDHA, LDHC, 2 more genes
    nsv4978462copy number variation1nstd200human GRCh38 chr11: 18,387,764-18,388,430 , GRCh37.p13 chr11: 18,409,311-18,409,977 MIR3159
    nsv4848832copy number variation1nstd200human GRCh37 chr11: 18,409,311-18,409,977 , GRCh38.p12 chr11: 18,387,764-18,388,430 MIR3159
    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
    nsv4680082copy number variation1nstd189human GRCh37.p13 chr11: 18,333,252-18,760,169 , GRCh38.p12 chr11: 18,311,705-18,738,622 , GTF2H1, 18 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
    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
    nsv4208761copy number variation1nstd166human GRCh37.p13 chr11: 18,133,425-18,936,070 , GRCh38.p12 chr11: 18,111,878-18,914,523 , UEVLD, 37 more genes
    nsv4202465copy number variation1nstd166human GRCh37.p13 chr11: 18,406,941-18,408,382 , GRCh38.p12 chr11: 18,385,394-18,386,835 MIR3159
    nsv3970658insertion1nstd168human GRCh38 chr11: 18,354,677-18,410,493 , GRCh37.p13 chr11: 18,376,224-18,432,040 GTF2H1, LDHA, 2 more genes
    nsv3957360complex substitution1nstd168human GRCh37.p13 chr11: 18,398,149-18,420,917 , GRCh38 chr11: 18,376,602-18,399,370 LDHA, MIR3159
    nsv3956588copy number variation1nstd168human GRCh38 chr11: 18,378,847-18,400,694 , GRCh37.p13 chr11: 18,400,394-18,422,241 LDHA, MIR3159
    nsv3919437copy number variation1nstd102humanPathogenic GRCh37 chr11: 17,926,636-19,696,051 , NCBI36 chr11: 17,883,212-19,652,627 , GRCh38 chr11: 17,905,089-19,674,505 CSRP3-AS1, ZDHHC13, 55 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
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