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Items: 1 to 20 of 210

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057933inversion1nstd229human GRCh38 chr7: 63,377,139-65,038,693 , GRCh37.p13 chr7: 62,837,517-64,499,071 , VN1R36P, 91 more genes
    nsv7046118inversion1nstd229human GRCh38 chr7: 64,922,598-65,231,396 , GRCh37.p13 chr7: 64,382,976-64,691,774 LOC441241, INTS4P1, 14 more genes
    nsv6837924copy number variation1nstd229human GRCh38 chr7: 64,965,916-64,972,275 , GRCh37.p13 chr7: 64,426,294-64,432,653 ERV3-1-ZNF117, VN1R43P, 1 more genes
    nsv6835419copy number variation1nstd229human GRCh38 chr7: 64,959,530-64,988,585 , GRCh37.p13 chr7: 64,419,908-64,448,963 ERV3-1, ERV3-1-ZNF117, 2 more genes
    nsv6832018copy number variation1nstd229human GRCh38 chr7: 64,981,389-64,985,769 , GRCh37.p13 chr7: 64,441,767-64,446,147 ZNF117, ERV3-1-ZNF117
    nsv6827973copy number variation1nstd229human GRCh38 chr7: 64,816,596-64,990,477 , GRCh37.p13 chr7: 64,276,974-64,450,855 ZNF138, ERV3-1-ZNF117, 9 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6632413copy number variation1nstd224human GRCh37 chr7: 62,241,041-64,438,809 , GRCh38.p12 chr7: 62,780,663-64,978,431 , ZNF138, 99 more genes
    nsv6613229copy number variation1nstd223human GRCh38 chr7: 64,935,601-64,976,600 , GRCh37.p13 chr7: 64,395,979-64,436,978 ZNF117, ERV3-1-ZNF117, 2 more genes
    nsv6606653copy number variation1nstd223human GRCh38 chr7: 64,959,530-64,988,582 , GRCh37.p13 chr7: 64,419,908-64,448,960 ERV3-1-ZNF117, ZNF117, 2 more genes
    nsv6571149inversion1nstd223human GRCh38 chr7: 64,985,026-64,985,755 , GRCh37.p13 chr7: 64,445,404-64,446,133 ZNF117, ERV3-1-ZNF117
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6293428mobile element insertion1nstd186human GRCh37 chr7: 64,442,606-64,442,657 , GRCh38.p12 chr7: 64,982,228-64,982,279 ZNF117, ERV3-1-ZNF117
    nsv6290777copy number variation1nstd102humanUncertain significance GRCh37 chr7: 64,052,765-64,651,336 , GRCh38.p12 chr7: 64,592,387-65,190,958 LOC441239, LOC644387, 24 more genes
    nsv6280711insertion1nstd214human GRCh38 chr7: 64,978,480-64,978,480 , GRCh37.p13 chr7: 64,438,858-64,438,858 ERV3-1-ZNF117, ZNF117
    nsv6175729copy number variation1nstd214human GRCh38 chr7: 64,977,675-64,977,758 , GRCh37.p13 chr7: 64,438,053-64,438,136 ZNF117, ERV3-1-ZNF117
    nsv6171873copy number variation1nstd214human GRCh38 chr7: 64,978,542-64,978,625 , GRCh37.p13 chr7: 64,438,920-64,439,003 ZNF117, ERV3-1-ZNF117
    nsv6136196copy number variation1nstd213human GRCh37 chr7: 62,900,000-64,980,001 , GRCh38.p12 chr7: 63,439,622-65,515,088 , ZNF138, 95 more genes
    nsv6135776copy number variation1nstd213human GRCh37 chr7: 64,360,000-64,980,001 , GRCh38.p12 chr7: 64,899,622-65,515,088 ZNF117, LOC441241, 21 more genes
    nsv6072117insertion1nstd212human GRCh38 chr7: 64,982,211-64,982,211 , GRCh37.p13 chr7: 64,442,589-64,442,589 ZNF117, ERV3-1-ZNF117
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