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Items: 1 to 20 of 987

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145122insertion1nstd232human GRCh37.p13 chr11: 99,432,454-99,432,454 , GRCh38.p12 chr11: 99,561,723-99,561,723 CNTN5
    nsv7145048insertion1nstd232human GRCh37.p13 chr11: 99,690,483-99,690,483 , GRCh38.p12 chr11: 99,819,752-99,819,752 CNTN5
    nsv7099286copy number variation4nstd231human GRCh37 chr11: 99,516,916-99,565,136 , GRCh38.p12 chr11: 99,646,185-99,694,405 CNTN5
    nsv7099285copy number variation1nstd231human GRCh37 chr11: 99,514,466-99,565,136 , GRCh38.p12 chr11: 99,643,735-99,694,405 CNTN5
    nsv7077403inversion1nstd229human GRCh38 chr11: 99,682,656-99,682,691 , GRCh37.p13 chr11: 99,553,387-99,553,422 CNTN5
    nsv7076299inversion1nstd229human GRCh38 chr11: 99,830,225-99,930,018 , GRCh37.p13 chr11: 99,700,956-99,800,750 CNTN5
    nsv7076205inversion1nstd229human GRCh38 chr11: 99,680,438-99,685,050 , GRCh37.p13 chr11: 99,551,169-99,555,781 CNTN5
    nsv7075616inversion1nstd229human GRCh38 chr11: 99,820,244-99,826,772 , GRCh37.p13 chr11: 99,690,975-99,697,503 CNTN5
    nsv7074799inversion1nstd229human GRCh38 chr11: 100,102,883-100,106,154 , GRCh37.p13 chr11: 99,973,615-99,976,886 CNTN5, LOC105369456
    nsv7073228inversion1nstd229human GRCh38 chr11: 100,198,999-100,199,104 , GRCh37.p13 chr11: 100,069,731-100,069,836 CNTN5
    nsv7073068inversion1nstd229human GRCh38 chr11: 99,176,251-99,219,450 , GRCh37.p13 chr11: 99,046,982-99,090,181 CNTN5
    nsv7073031inversion1nstd229human GRCh38 chr11: 99,981,055-99,983,799 , GRCh37.p13 chr11: 99,851,787-99,854,531 CNTN5
    nsv7072949inversion1nstd229human GRCh38 chr11: 99,582,506-99,593,563 , GRCh37.p13 chr11: 99,453,237-99,464,294 CNTN5
    nsv7070896inversion1nstd229human GRCh38 chr11: 98,256,422-99,630,063 , GRCh37.p13 chr11: 98,127,150-99,500,794 CNTN5, RN7SKP53, 3 more genes
    nsv7070425inversion1nstd229human GRCh38 chr11: 100,116,010-100,895,806 , GRCh37.p13 chr11: 99,986,742-100,766,537 CNTN5, ARHGAP42, 6 more genes
    nsv7070134inversion1nstd229human GRCh38 chr11: 99,289,722-99,314,838 , GRCh37.p13 chr11: 99,160,453-99,185,569 CNTN5
    nsv7070074inversion1nstd229human GRCh38 chr11: 99,680,435-99,680,585 , GRCh37.p13 chr11: 99,551,166-99,551,316 CNTN5
    nsv7068147inversion1nstd229human GRCh38 chr11: 99,086,229-99,086,282 , GRCh37.p13 chr11: 98,956,959-98,957,012 CNTN5
    nsv7067691inversion1nstd229human GRCh38 chr11: 98,258,241-99,630,062 , GRCh37.p13 chr11: 98,128,969-99,500,793 CNTN5, LOC643381, 3 more genes
    nsv7063773inversion1nstd229human GRCh38 chr11: 99,990,851-99,990,961 , GRCh37.p13 chr11: 99,861,583-99,861,693 CNTN5
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