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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv6890060copy number variation1nstd229human GRCh38 chr10: 63,146,809-63,149,262 , GRCh37.p13 chr10: 64,906,569-64,909,022 NRBF2
    nsv6882608copy number variation1nstd229human GRCh38 chr10: 63,143,593-63,146,147 , GRCh37.p13 chr10: 64,903,353-64,905,907 NRBF2
    nsv6586147inversion1nstd223human GRCh38 chr10: 63,138,619-63,139,180 , GRCh37.p13 chr10: 64,898,379-64,898,940 NRBF2
    nsv6309000copy number variation2nstd102humanUncertain significance GRCh37 chr10: 64,572,967-65,225,422 , GRCh38.p12 chr10: 62,813,207-63,465,662 JMJD1C-AS2, TATDN1P1, 9 more genes
    nsv6247147mobile element insertion1nstd215human GRCh38 chr10: 63,149,760-63,149,760 , GRCh37.p13 chr10: 64,909,520-64,909,520 NRBF2
    nsv6131796copy number variation1nstd213human GRCh37 chr10: 64,600,000-65,090,001 , GRCh38.p12 chr10: 62,840,240-63,330,241 NRBF2, JMJD1C, 4 more genes
    nsv6088712insertion1nstd212human GRCh38 chr10: 63,146,132-63,146,132 , GRCh37.p13 chr10: 64,905,892-64,905,892 NRBF2
    nsv6087614insertion1nstd212human GRCh38 chr10: 63,134,004-63,134,004 , GRCh37.p13 chr10: 64,893,764-64,893,764 NRBF2
    nsv5727779mobile element insertion1nstd211human GRCh38 chr10: 63,146,132-63,146,132 , GRCh37.p13 chr10: 64,905,892-64,905,892 NRBF2
    nsv5713446mobile element insertion1nstd211human GRCh38 chr10: 63,146,145-63,146,145 , GRCh37.p13 chr10: 64,905,905-64,905,905 NRBF2
    nsv5625104insertion1nstd207human GRCh38 chr10: 63,133,977-63,133,977 , GRCh37.p13 chr10: 64,893,737-64,893,737 NRBF2
    nsv5410127mobile element insertion1nstd206human GRCh38 chr10: 63,146,145-63,146,196 , GRCh37.p13 chr10: 64,905,905-64,905,956 NRBF2
    nsv5191205mobile element insertion1nstd203human GRCh38 chr10: 63,146,119-63,146,119 , GRCh37.p13 chr10: 64,905,879-64,905,879 NRBF2
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4976041copy number variation1nstd200human GRCh38 chr10: 63,155,034-63,161,840 , GRCh37.p13 chr10: 64,914,794-64,921,600 NRBF2
    nsv4831370copy number variation1nstd200human GRCh37 chr10: 64,914,794-64,921,600 , GRCh38.p12 chr10: 63,155,034-63,161,840 NRBF2
    nsv4761766insertion1nstd199human GRCh37 chr10: 64,893,730-64,893,730 , GRCh38.p12 chr10: 63,133,970-63,133,970 NRBF2
    nsv4675455copy number variation1nstd102humanPathogenic GRCh37 chr10: 50,250,603-69,256,083 , GRCh38.p12 chr10: 45,931,517-67,496,325 MRLN, LOC102724778, 242 more genes
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