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Items: 1 to 20 of 261

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979069insertion1nstd209human GRCh38 chr20: 25,248,020-25,248,020 , GRCh37.p13 chr20: 25,228,656-25,228,656 PYGB
    nsv5960629copy number variation1nstd209human GRCh38 chr20: 24,517,514-25,490,454 , GRCh37.p13 chr20: 24,498,150-25,471,090 LOC105372581, LOC107985402, 18 more genes
    nsv5695883mobile element insertion1nstd211human GRCh38 chr20: 25,249,083-25,249,083 , GRCh37.p13 chr20: 25,229,719-25,229,719 PYGB
    nsv5671881insertion1nstd207human GRCh38 chr20: 25,248,020-25,248,020 , GRCh37.p13 chr20: 25,228,656-25,228,656 PYGB
    nsv5664609insertion1nstd207human GRCh38 chr20: 25,290,940-25,290,940 , GRCh37.p13 chr20: 25,271,576-25,271,576 PYGB
    nsv5530717copy number variation1nstd206human GRCh38 chr20: 25,121,452-25,367,703 , GRCh37.p13 chr20: 25,102,088-25,348,339 ENTPD6, PYGB, 6 more genes
    nsv5530221copy number variation1nstd206human GRCh38 chr20: 25,262,429-25,262,601 , GRCh37.p13 chr20: 25,243,065-25,243,237 PYGB
    nsv5521147copy number variation1nstd206human GRCh38 chr20: 25,266,569-25,268,077 , GRCh37.p13 chr20: 25,247,205-25,248,713 PYGB
    nsv5418833mobile element insertion1nstd206human GRCh38 chr20: 25,249,083-25,249,134 , GRCh37.p13 chr20: 25,229,719-25,229,770 PYGB
    nsv5366221translocation1nstd200human GRCh37.p13 chr2: 55,362,187-55,362,187 , GRCh38 chr2: 55,135,051-55,135,051 , GRCh38 chr20: 25,249,287-25,249,287 , GRCh37.p13 chr20: 25,229,923-25,229,923 PYGB, RTN4
    nsv5366218translocation1nstd200human GRCh38 chr2: 55,134,732-55,134,732 , GRCh38 chr20: 25,249,285-25,249,285 , GRCh37.p13 chr2: 55,361,868-55,361,868 , GRCh37.p13 chr20: 25,229,921-25,229,921 PYGB, RTN4
    nsv5323867copy number variation1nstd204human GRCh37.p13 chr20: 25,275,308-25,275,684 , GRCh38.p13 chr20: 25,294,672-25,295,048 PYGB, ABHD12
    nsv5162641mobile element insertion1nstd203human GRCh38 chr20: 25,289,481-25,289,497 , GRCh37.p13 chr20: 25,270,117-25,270,133 PYGB
    nsv5025236copy number variation1nstd200human GRCh38 chr20: 25,173,293-25,314,337 , GRCh37.p13 chr20: 25,153,929-25,294,973 LOC101926889, LOC105372579, 3 more genes
    nsv5021829copy number variation1nstd200human GRCh38 chr20: 25,286,246-25,288,612 , GRCh37.p13 chr20: 25,266,882-25,269,248 PYGB
    nsv4862405copy number variation1nstd200human GRCh37 chr20: 25,275,316-25,275,676 , GRCh38.p12 chr20: 25,294,680-25,295,040 ABHD12, PYGB
    nsv4862404copy number variation1nstd200human GRCh37 chr20: 25,229,218-25,232,795 , GRCh38.p12 chr20: 25,248,582-25,252,159 PYGB
    nsv4766434insertion1nstd199human GRCh37 chr20: 25,228,622-25,228,622 , GRCh38.p12 chr20: 25,247,986-25,247,986 PYGB
    nsv4729757copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 19,750,804-30,479,077 , GRCh38.p12 chr20: 19,770,160-31,891,274 BCL2L1, CD24P3, 222 more genes
    nsv4724474insertion1nstd186human GRCh37 chr20: 25,228,616-25,228,616 , GRCh38.p12 chr20: 25,247,980-25,247,980 PYGB
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