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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7055208inversion1nstd229human GRCh38 chr5: 31,280,121-31,280,149 , GRCh37.p13 chr5: 31,280,228-31,280,256 CDH6
    nsv7054903inversion1nstd229human GRCh38 chr5: 31,211,666-31,215,826 , GRCh37.p13 chr5: 31,211,773-31,215,933 LOC105374709, CDH6
    nsv7044414inversion1nstd229human GRCh38 chr5: 31,291,313-31,291,460 , GRCh37.p13 chr5: 31,291,420-31,291,567 CDH6
    nsv7042253inversion1nstd229human GRCh38 chr5: 31,234,490-31,234,554 , GRCh37.p13 chr5: 31,234,597-31,234,661 CDH6
    nsv7041737inversion1nstd229human GRCh38 chr5: 31,211,143-31,220,279 , GRCh37.p13 chr5: 31,211,250-31,220,386 CDH6, LOC105374709
    nsv6777097copy number variation1nstd229human GRCh38 chr5: 31,001,934-31,214,346 , GRCh37.p13 chr5: 31,002,041-31,214,453 RPL19P11, LOC105374709, 1 more genes
    nsv6774450copy number variation1nstd229human GRCh38 chr5: 31,192,601-31,472,600 , GRCh37.p13 chr5: 31,192,708-31,472,707 LOC105374709, DUX4L51, 2 more genes
    nsv6773912copy number variation1nstd229human GRCh38 chr5: 31,214,254-31,214,393 , GRCh37.p13 chr5: 31,214,361-31,214,500 CDH6, LOC105374709
    nsv6773701copy number variation1nstd229human GRCh38 chr5: 31,262,501-31,277,200 , GRCh37.p13 chr5: 31,262,608-31,277,307 CDH6
    nsv6773242copy number variation1nstd229human GRCh38 chr5: 31,220,760-31,224,538 , GRCh37.p13 chr5: 31,220,867-31,224,645 CDH6
    nsv6770690copy number variation1nstd229human GRCh38 chr5: 31,183,432-31,200,698 , GRCh37.p13 chr5: 31,183,539-31,200,805 CDH6, LOC105374709
    nsv6766606copy number variation1nstd229human GRCh38 chr5: 31,204,862-31,209,200 , GRCh37.p13 chr5: 31,204,969-31,209,307 LOC105374709, CDH6
    nsv6765647copy number variation1nstd229human GRCh38 chr5: 31,232,101-31,237,200 , GRCh37.p13 chr5: 31,232,208-31,237,307 CDH6
    nsv6764672copy number variation1nstd229human GRCh38 chr5: 31,274,267-31,277,046 , GRCh37.p13 chr5: 31,274,374-31,277,153 CDH6
    nsv6763076copy number variation1nstd229human GRCh38 chr5: 31,249,190-31,252,398 , GRCh37.p13 chr5: 31,249,297-31,252,505 CDH6, DUX4L51
    nsv6762939copy number variation1nstd229human GRCh38 chr5: 31,188,640-31,193,775 , GRCh37.p13 chr5: 31,188,747-31,193,882 CDH6
    nsv6761647copy number variation1nstd229human GRCh38 chr5: 31,082,736-31,663,838 , GRCh37.p13 chr5: 31,082,843-31,663,945 C5orf22, DROSHA, 5 more genes
    nsv6758736copy number variation1nstd229human GRCh38 chr5: 31,202,436-31,208,296 , GRCh37.p13 chr5: 31,202,543-31,208,403 LOC105374709, CDH6
    nsv6758387copy number variation1nstd229human GRCh38 chr5: 31,227,228-31,228,069 , GRCh37.p13 chr5: 31,227,335-31,228,176 CDH6
    nsv6636973copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,348,753-46,389,339 , GRCh38.p12 chr5: 29,348,646-46,389,237 SUB1, LOC105374740, 210 more genes
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