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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5925282copy number variation1nstd209human GRCh38 chr11: 9,623,316-10,133,753 , GRCh37.p13 chr11: 9,644,863-10,155,300 SWAP70, LOC101928008, 8 more genes
    nsv5912011copy number variation1nstd209human GRCh38 chr11: 9,623,387-10,133,591 , GRCh37.p13 chr11: 9,644,934-10,155,138 RN7SKP50, RPL21P97, 8 more genes
    nsv5554128sequence alteration1nstd206human GRCh38 chr11: 9,753,510-9,753,510 , GRCh37.p13 chr11: 9,775,057-9,775,057 LINC02709
    nsv5354720translocation1nstd200human GRCh38 chr11: 9,753,510-9,753,510 , GRCh38 chr11: 9,798,482-9,798,482 , GRCh37.p13 chr11: 9,775,057-9,775,057 , GRCh37.p13 chr11: 9,820,029-9,820,029 SBF2, SBF2-AS1, 1 more genes
    nsv4984191copy number variation1nstd200human GRCh38 chr11: 9,730,808-9,764,206 , GRCh37.p13 chr11: 9,752,355-9,785,753 LINC02709, SBF2-AS1, 1 more genes
    nsv4978204copy number variation1nstd200human GRCh38 chr11: 9,757,774-9,766,436 , GRCh37.p13 chr11: 9,779,321-9,787,983 LINC02709, SBF2-AS1
    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
    nsv4680411copy number variation1nstd189human GRCh37.p13 chr11: 9,358,141-9,813,308 , GRCh38.p12 chr11: 9,336,594-9,791,761 WEE1, ZNF143, 11 more genes
    nsv4679723copy number variation1nstd189human GRCh37.p13 chr11: 9,647,838-10,160,052 , GRCh38.p12 chr11: 9,626,291-10,138,505 GLULP2, SWAP70, 8 more genes
    nsv4679528copy number variation1nstd189human GRCh37.p13 chr11: 9,640,887-10,164,410 , GRCh38.p12 chr11: 9,619,340-10,142,863 GLULP2, SWAP70, 8 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
    nsv4616855copy number variation1nstd183human GRCh37 chr11: 9,645,441-10,152,438 , GRCh38.p12 chr11: 9,623,894-10,130,891 SBF2-AS1, RNU7-28P, 8 more genes
    nsv4613010copy number variation2nstd183human GRCh37 chr11: 9,779,266-9,779,325 , GRCh38.p12 chr11: 9,757,719-9,757,778 LINC02709, SBF2-AS1
    nsv4599100copy number variation1nstd183human GRCh37 chr11: 9,647,837-10,150,593 , GRCh38.p12 chr11: 9,626,290-10,129,046 RPL21P97, RN7SKP50, 8 more genes
    nsv4561435sequence alteration1nstd166human GRCh37.p13 chr11: 9,775,057-9,775,058 , GRCh38.p12 chr11: 9,753,510-9,753,511 LINC02709
    nsv4374873copy number variation1nstd173human GRCh37 chr11: 9,648,324-9,844,858 , GRCh38.p12 chr11: 9,626,777-9,823,311 LOC105369149, RN7SKP50, 5 more genes
    nsv4367321copy number variation1nstd173human GRCh37 chr11: 9,422,923-11,175,143 , GRCh38.p12 chr11: 9,401,376-11,153,596 , LOC107984309, 40 more genes
    nsv4350476copy number variation1nstd102humanPathogenic GRCh37 chr11: 193,146-12,643,136 , GRCh38.p12 chr11: 193,146-12,621,589 KRTAP5-3, OR56A7P, 457 more genes
    nsv3923443copy number variation1nstd102humanUncertain significance NCBI36 chr11: 7,973,799-10,415,328 , GRCh37 chr11: 8,017,223-10,458,752 , GRCh38 chr11: 7,995,676-10,437,205 TMEM41B, AKIP1, 51 more genes
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