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Items: 1 to 20 of 354

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7062837inversion1nstd229human GRCh38 chr11: 40,841,838-44,720,409 , GRCh37.p13 chr11: 40,863,388-44,741,959 TTC17, ACCSL, 35 more genes
    nsv6916553copy number variation1nstd229human GRCh38 chr11: 43,408,161-43,408,296 , GRCh37.p13 chr11: 43,429,711-43,429,846 TTC17
    nsv6913612copy number variation1nstd229human GRCh38 chr11: 43,362,236-43,368,357 , GRCh37.p13 chr11: 43,383,786-43,389,907 TTC17
    nsv6913421copy number variation1nstd229human GRCh38 chr11: 43,358,431-43,567,029 , GRCh37.p13 chr11: 43,379,981-43,588,579 CTBP2P6, MIR670, 2 more genes
    nsv6912419copy number variation1nstd229human GRCh38 chr11: 43,361,074-43,361,194 , GRCh37.p13 chr11: 43,382,624-43,382,744 TTC17
    nsv6910212copy number variation1nstd229human GRCh38 chr11: 43,455,082-43,463,317 , GRCh37.p13 chr11: 43,476,632-43,484,867 TTC17
    nsv6908495copy number variation1nstd229human GRCh38 chr11: 43,479,044-43,482,340 , GRCh37.p13 chr11: 43,500,594-43,503,890 TTC17
    nsv6907875copy number variation1nstd229human GRCh38 chr11: 43,411,643-43,414,398 , GRCh37.p13 chr11: 43,433,193-43,435,948 TTC17
    nsv6907570copy number variation1nstd229human GRCh38 chr11: 43,469,773-43,469,925 , GRCh37.p13 chr11: 43,491,323-43,491,475 TTC17
    nsv6906576copy number variation1nstd229human GRCh38 chr11: 43,426,115-43,426,206 , GRCh37.p13 chr11: 43,447,665-43,447,756 TTC17
    nsv6905122copy number variation1nstd229human GRCh38 chr11: 43,434,212-43,434,235 , GRCh37.p13 chr11: 43,455,762-43,455,785 TTC17, RN7SKP287
    nsv6904997copy number variation1nstd229human GRCh38 chr11: 43,412,206-43,412,392 , GRCh37.p13 chr11: 43,433,756-43,433,942 TTC17
    nsv6901314copy number variation1nstd229human GRCh38 chr11: 43,487,245-43,689,403 , GRCh37.p13 chr11: 43,508,795-43,710,953 MIR129-2, MIR670HG, 4 more genes
    nsv6901237copy number variation1nstd229human GRCh38 chr11: 43,457,803-43,463,842 , GRCh37.p13 chr11: 43,479,353-43,485,392 TTC17
    nsv6900496copy number variation1nstd229human GRCh38 chr11: 43,384,559-43,384,608 , GRCh37.p13 chr11: 43,406,109-43,406,158 TTC17
    nsv6899839copy number variation1nstd229human GRCh38 chr11: 43,356,543-43,362,699 , GRCh37.p13 chr11: 43,378,093-43,384,249 TTC17
    nsv6593158inversion1nstd223human GRCh38 chr11: 43,482,057-43,484,181 , GRCh37.p13 chr11: 43,503,607-43,505,731 TTC17
    nsv6591730inversion1nstd223human GRCh38 chr11: 43,383,460-43,383,943 , GRCh37.p13 chr11: 43,405,010-43,405,493 TTC17
    nsv6589870inversion1nstd223human GRCh38 chr11: 43,481,880-43,484,089 , GRCh37.p13 chr11: 43,503,430-43,505,639 TTC17
    nsv6587372inversion1nstd223human GRCh38 chr11: 43,365,987-43,366,396 , GRCh37.p13 chr11: 43,387,537-43,387,946 TTC17
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