U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 142

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7070638inversion1nstd229human GRCh38 chr17: 20,843,363-22,437,673 , GRCh37.p13 chr17: 20,746,676-21,937,002 LOC107987246, PDLIM1P2, 33 more genes
    nsv6993424copy number variation1nstd229human GRCh38 chr17: 21,207,653-21,209,533 , GRCh37.p13 chr17: 21,110,966-21,112,846 TMEM11
    nsv6990787copy number variation1nstd229human GRCh38 chr17: 21,203,874-21,208,225 , GRCh37.p13 chr17: 21,107,187-21,111,538 TMEM11
    nsv6989220copy number variation1nstd229human GRCh38 chr17: 21,203,454-21,208,221 , GRCh37.p13 chr17: 21,106,767-21,111,534 TMEM11
    nsv6985675copy number variation1nstd229human GRCh38 chr17: 21,204,501-21,208,400 , GRCh37.p13 chr17: 21,107,814-21,111,713 TMEM11
    nsv6985622copy number variation1nstd229human GRCh38 chr17: 21,209,901-21,213,200 , GRCh37.p13 chr17: 21,113,214-21,116,513 TMEM11-DT, TMEM11
    nsv6983173copy number variation1nstd229human GRCh38 chr17: 21,203,601-21,208,700 , GRCh37.p13 chr17: 21,106,914-21,112,013 TMEM11
    nsv6502353copy number variation1nstd223human GRCh38 chr17: 21,111,202-21,303,044 , GRCh37.p13 chr17: 21,014,515-21,206,356 EIF1P5, MAP2K3, 5 more genes
    nsv6499885copy number variation1nstd223human GRCh38 chr17: 21,203,901-21,205,400 , GRCh37.p13 chr17: 21,107,214-21,108,713 TMEM11
    nsv6499286copy number variation1nstd223human GRCh38 chr17: 21,203,801-21,207,200 , GRCh37.p13 chr17: 21,107,114-21,110,513 TMEM11
    nsv6315238complex substitution1nstd102humanPathogenic GRCh37 chr17: 14,876,984-22,124,952 , GRCh38.p12 chr17: 14,973,667-22,625,625 ADORA2B, ALDH3A1, 281 more genes
    nsv5941901copy number variation1nstd209human GRCh38 chr17: 21,203,874-21,208,224 , GRCh37.p13 chr17: 21,107,187-21,111,537 TMEM11
    nsv5869091copy number variation1nstd209human GRCh38 chr17: 21,203,895-21,208,178 , GRCh37.p13 chr17: 21,107,208-21,111,491 TMEM11
    nsv5670902inversion1nstd207human GRCh37.p13 chr17: 19,143,942-21,250,947 , GRCh38 chr17: 19,240,629-21,558,840 , ALDH3A1, 86 more genes
    nsv5519266copy number variation1nstd206human GRCh38 chr17: 21,203,876-21,208,225 , GRCh37.p13 chr17: 21,107,189-21,111,538 TMEM11
    nsv5335321translocation1nstd200human GRCh37 chr17: 21,111,538-21,111,538 , GRCh37 chr17: 21,107,189-21,107,189 , GRCh38.p12 chr17: 21,203,876-21,203,876 , GRCh38.p12 chr17: 21,208,225-21,208,225 TMEM11
    nsv5324095copy number variation1nstd204human GRCh38.p13 chr17: 21,203,871-21,208,226 , GRCh37.p13 chr17: 21,107,184-21,111,539 TMEM11
    nsv5294494copy number variation1nstd204human GRCh38.p13 chr17: 21,204,179-21,208,278 , GRCh37.p13 chr17: 21,107,492-21,111,591 TMEM11
    nsv5292336copy number variation1nstd204human GRCh38.p13 chr17: 21,202,201-21,209,300 , GRCh37.p13 chr17: 21,105,514-21,112,613 TMEM11
    nsv5026271copy number variation1nstd200human GRCh38 chr17: 21,203,876-21,208,225 , GRCh37.p13 chr17: 21,107,189-21,111,538 TMEM11
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Find related data

    Recent activity

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    Support Center