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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5921558copy number variation1nstd209human GRCh38 chr11: 71,467,840-71,468,679 , GRCh37.p13 chr11: 71,178,886-71,179,725 NADSYN1
    nsv5907858copy number variation1nstd209human GRCh38 chr11: 71,501,699-71,504,675 , GRCh37.p13 chr11: 71,212,745-71,215,721 S100A11P3, NADSYN1
    nsv5859669copy number variation1nstd209human GRCh38 chr11: 71,501,717-71,504,716 , GRCh37.p13 chr11: 71,212,763-71,215,762 S100A11P3, NADSYN1
    nsv5585222copy number variation1nstd207human GRCh38 chr11: 71,474,711-71,474,782 , GRCh37.p13 chr11: 71,185,757-71,185,828 NADSYN1
    nsv5584848copy number variation1nstd207human GRCh38 chr11: 71,501,699-71,504,675 , GRCh37.p13 chr11: 71,212,745-71,215,721 S100A11P3, NADSYN1
    nsv5499427copy number variation1nstd206human GRCh38 chr11: 71,501,700-71,504,676 , GRCh37.p13 chr11: 71,212,746-71,215,722 S100A11P3, NADSYN1
    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
    nsv5373701translocation1nstd200human GRCh38 chr11: 71,450,716-71,450,716 , GRCh38 chr11: 71,451,846-71,451,846 , GRCh37.p13 chr11: 71,161,762-71,161,762 , GRCh37.p13 chr11: 71,162,892-71,162,892 NADSYN1
    nsv5355349translocation1nstd200human GRCh38 chr11: 71,467,843-71,467,843 , GRCh38 chr11: 71,468,680-71,468,680 , GRCh37.p13 chr11: 71,178,889-71,178,889 , GRCh37.p13 chr11: 71,179,726-71,179,726 NADSYN1
    nsv5355348translocation1nstd200human GRCh38 chr11: 71,450,917-71,450,917 , GRCh38 chr11: 71,451,854-71,451,854 , GRCh37.p13 chr11: 71,162,900-71,162,900 , GRCh37.p13 chr11: 71,161,963-71,161,963 NADSYN1
    nsv5333190translocation1nstd200human GRCh37 chr11: 71,178,546-71,178,546 , GRCh37 chr11: 71,179,724-71,179,724 , GRCh38.p12 chr11: 71,467,500-71,467,500 , GRCh38.p12 chr11: 71,468,678-71,468,678 NADSYN1
    nsv5331943translocation1nstd200human GRCh37 chr11: 71,178,889-71,178,889 , GRCh37 chr11: 71,179,726-71,179,726 , GRCh38.p12 chr11: 71,467,843-71,467,843 , GRCh38.p12 chr11: 71,468,680-71,468,680 NADSYN1
    nsv4980091copy number variation1nstd200human GRCh38 chr11: 71,501,700-71,504,676 , GRCh37.p13 chr11: 71,212,746-71,215,722 S100A11P3, NADSYN1
    nsv4846655copy number variation1nstd200human GRCh37 chr11: 71,212,746-71,215,722 , GRCh38.p12 chr11: 71,501,700-71,504,676 S100A11P3, NADSYN1
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4747262copy number variation1nstd199human GRCh37 chr11: 71,213,357-71,213,552 , GRCh38.p12 chr11: 71,502,311-71,502,506 NADSYN1
    nsv4715246copy number variation1nstd195human GRCh37 chr11: 70,879,801-71,222,251 , GRCh38.p12 chr11: 71,168,755-71,511,205 DHCR7, SHANK2, 4 more genes
    nsv4681893copy number variation1nstd102humanUncertain significance GRCh37 chr11: 71,146,401-71,907,241 , GRCh38.p12 chr11: 71,435,355-72,196,197 OR7E128P, ZNF705EP, 39 more genes
    nsv4618361copy number variation1nstd183human GRCh37 chr11: 71,212,745-71,215,722 , GRCh38.p12 chr11: 71,501,699-71,504,676 S100A11P3, NADSYN1
    nsv4613185copy number variation2nstd183human GRCh37 chr11: 71,212,774-71,215,694 , GRCh38.p12 chr11: 71,501,728-71,504,648 S100A11P3, NADSYN1
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