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Items: 1 to 20 of 202

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5939032copy number variation1nstd209human GRCh38 chr19: 55,700,286-55,702,801 , GRCh37.p13 chr19: 56,211,652-56,214,167 EPN1
    nsv5935857copy number variation1nstd209human GRCh38 chr19: 55,709,313-55,716,660 , GRCh37.p13 chr19: 56,220,679-56,228,026 NLRP9, EPN1
    nsv5933151copy number variation1nstd209human GRCh38 chr19: 55,700,114-55,700,578 , GRCh37.p13 chr19: 56,211,480-56,211,944 EPN1
    nsv5873551copy number variation1nstd209human GRCh38 chr19: 55,700,352-55,703,172 , GRCh37.p13 chr19: 56,211,718-56,214,538 EPN1
    nsv5867761copy number variation1nstd209human GRCh38 chr19: 55,709,275-55,716,663 , GRCh37.p13 chr19: 56,220,641-56,228,029 EPN1, NLRP9
    nsv5591534copy number variation1nstd207human GRCh38 chr19: 55,700,114-55,700,578 , GRCh37.p13 chr19: 56,211,480-56,211,944 EPN1
    nsv5530162copy number variation1nstd206human GRCh38 chr19: 55,709,729-55,709,885 , GRCh37.p13 chr19: 56,221,095-56,221,251 NLRP9, EPN1
    nsv5527080copy number variation1nstd206human GRCh38 chr19: 55,702,830-55,703,359 , GRCh37.p13 chr19: 56,214,196-56,214,725 EPN1
    nsv5519413copy number variation1nstd206human GRCh38 chr19: 55,700,117-55,700,579 , GRCh37.p13 chr19: 56,211,483-56,211,945 EPN1
    nsv5327672translocation1nstd204human GRCh38.p13 chr19: 55,700,117-55,700,117 , GRCh38.p13 chr19: 55,700,579-55,700,579 , GRCh37.p13 chr19: 56,211,945-56,211,945 , GRCh37.p13 chr19: 56,211,483-56,211,483 EPN1
    nsv5294450copy number variation1nstd204human GRCh38.p13 chr19: 55,700,101-55,700,600 , GRCh37.p13 chr19: 56,211,467-56,211,966 EPN1
    nsv5209336mobile element deletion1nstd204human GRCh38.p13 chr19: 55,701,953-55,702,265 , GRCh37.p13 chr19: 56,213,319-56,213,631 EPN1
    nsv5028100copy number variation1nstd200human GRCh38 chr19: 55,700,117-55,700,579 , GRCh37.p13 chr19: 56,211,483-56,211,945 EPN1
    nsv5028099copy number variation1nstd200human GRCh38 chr19: 55,699,014-55,700,178 , GRCh37.p13 chr19: 56,210,380-56,211,544 EPN1
    nsv5028098copy number variation1nstd200human GRCh38 chr19: 55,697,540-55,700,961 , GRCh37.p13 chr19: 56,208,906-56,212,327 EPN1
    nsv5028097copy number variation1nstd200human GRCh38 chr19: 55,682,538-55,682,640 , GRCh37.p13 chr19: 56,193,904-56,194,006 EPN1
    nsv5024973copy number variation1nstd200human GRCh38 chr19: 55,709,729-55,709,885 , GRCh37.p13 chr19: 56,221,095-56,221,251 EPN1, NLRP9
    nsv4907574mobile element deletion1nstd200human GRCh38 chr19: 55,701,962-55,702,257 , GRCh37.p13 chr19: 56,213,328-56,213,623 EPN1
    nsv4865351copy number variation1nstd200human GRCh37 chr19: 56,221,095-56,221,251 , GRCh38.p12 chr19: 55,709,729-55,709,885 NLRP9, EPN1
    nsv4861415copy number variation1nstd200human GRCh37 chr19: 56,211,483-56,211,945 , GRCh38.p12 chr19: 55,700,117-55,700,579 EPN1
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