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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112707copy number variation1nstd102humanUncertain significance GRCh38 chr1: 6,234,122-6,508,845 , GRCh37.p13 chr1: 6,294,182-6,568,905 HES3, PLEKHG5, 8 more genes
    nsv6112685copy number variation1nstd102humannot provided GRCh37 chr1: 2,420,003-8,155,935 , GRCh38.p12 chr1: 2,488,564-8,095,875 LINC02780, C1orf174, 100 more genes
    nsv5876958copy number variation1nstd209human GRCh38 chr1: 6,436,945-6,437,016 , GRCh37.p13 chr1: 6,497,005-6,497,076 ESPN
    nsv5830725copy number variation1nstd209human GRCh38 chr1: 6,435,780-6,438,046 , GRCh37.p13 chr1: 6,495,840-6,498,106 ESPN
    nsv5621276insertion1nstd207human GRCh38 chr1: 6,448,901-6,448,901 , GRCh37.p13 chr1: 6,508,961-6,508,961 ESPN
    nsv5619285insertion1nstd207human GRCh38 chr1: 6,429,311-6,429,311 , GRCh37.p13 chr1: 6,489,371-6,489,371 ESPN, MIR4252
    nsv5583310copy number variation1nstd207human GRCh38 chr1: 6,438,281-6,438,469 , GRCh37.p13 chr1: 6,498,341-6,498,529 ESPN
    nsv5574847copy number variation1nstd207human GRCh38 chr1: 6,442,576-6,442,866 , GRCh37.p13 chr1: 6,502,636-6,502,926 ESPN
    nsv5568949copy number variation1nstd207human GRCh38 chr1: 6,436,893-6,436,964 , GRCh37.p13 chr1: 6,496,953-6,497,024 ESPN
    nsv5567010copy number variation1nstd207human GRCh38 chr1: 6,438,388-6,438,469 , GRCh37.p13 chr1: 6,498,448-6,498,529 ESPN
    nsv5428818copy number variation1nstd206human GRCh38 chr1: 6,430,632-6,430,998 , GRCh37.p13 chr1: 6,490,692-6,491,058 ESPN
    nsv4889609copy number variation1nstd200human GRCh38 chr1: 6,418,665-6,424,166 , GRCh37.p13 chr1: 6,478,725-6,484,226 ESPN, HES2
    nsv4782741copy number variation1nstd200human GRCh37 chr1: 6,490,692-6,491,058 , GRCh38.p12 chr1: 6,430,632-6,430,998 ESPN
    nsv4782740copy number variation1nstd200human GRCh37 chr1: 6,478,725-6,484,226 , GRCh38.p12 chr1: 6,418,665-6,424,166 HES2, ESPN
    nsv4685972copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 762,080-7,309,686 , GRCh38.p12 chr1: 826,700-7,249,626 CDK11B, DFFB, 184 more genes
    nsv4674407copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,466-7,786,545 , GRCh38.p12 chr1: 914,086-7,726,485 MMP23B, RNF223, 183 more genes
    nsv4662273copy number variation2nstd186human GRCh37 chr1: 6,481,741-6,515,522 , GRCh38.p12 chr1: 6,421,681-6,455,462 MIR4252, ESPN
    nsv4594618copy number variation1nstd183human GRCh37 chr1: 6,504,836-6,505,937 , GRCh38.p12 chr1: 6,444,776-6,445,877 ESPN
    nsv4594617copy number variation2nstd183human GRCh37 chr1: 6,501,036-6,501,081 , GRCh38.p12 chr1: 6,440,976-6,441,021 ESPN
    nsv4594612copy number variation1nstd183human GRCh37 chr1: 6,403,048-6,577,424 , GRCh38.p12 chr1: 6,342,988-6,517,364 TNFRSF25, ACOT7, 4 more genes
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