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Items: 1 to 20 of 138

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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
    nsv6835490copy number variation1nstd229human GRCh38 chr7: 64,582,964-64,585,379 , GRCh37.p13 chr7: 64,043,342-64,045,757 LOC100128885, LOC641746
    nsv6834146copy number variation1nstd229human GRCh38 chr7: 64,573,940-64,632,511 , GRCh37.p13 chr7: 64,034,318-64,092,889 LOC105375326, LOC100128885, 1 more genes
    nsv6831197copy number variation1nstd229human GRCh38 chr7: 64,520,099-64,701,533 , GRCh37.p13 chr7: 63,980,477-64,161,911 LOC641746, LOC105375326, 8 more genes
    nsv6824626copy number variation1nstd229human GRCh38 chr7: 64,530,721-64,659,868 , GRCh37.p13 chr7: 63,991,099-64,120,246 LOC100128885, LOC100129293, 5 more genes
    nsv6818340copy number variation1nstd229human GRCh38 chr7: 64,462,374-64,808,082 , GRCh37.p13 chr7: 63,922,752-64,268,460 LOC100133092, ZNF138, 13 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
    nsv6631917copy number variation1nstd224human GRCh37 chr7: 64,034,536-64,105,259 , GRCh38.p12 chr7: 64,574,158-64,644,881 LOC641746, LOC100128885, 1 more genes
    nsv6618046copy number variation1nstd223human GRCh38 chr7: 64,520,099-64,701,532 , GRCh37.p13 chr7: 63,980,477-64,161,910 LOC641746, LOC100129293, 8 more genes
    nsv6612849copy number variation1nstd223human GRCh38 chr7: 64,581,329-64,585,817 , GRCh37.p13 chr7: 64,041,707-64,046,195 LOC641746, LOC100128885
    nsv6612735copy number variation1nstd223human GRCh38 chr7: 64,575,764-64,580,746 , GRCh37.p13 chr7: 64,036,142-64,041,124 LOC641746, LOC100128885
    nsv6605721copy number variation1nstd223human GRCh38 chr7: 64,582,601-64,583,000 , GRCh37.p13 chr7: 64,042,979-64,043,378 LOC100128885, LOC641746
    nsv6562895inversion1nstd223human GRCh38 chr7: 64,580,499-64,580,907 , GRCh37.p13 chr7: 64,040,877-64,041,285 LOC641746, LOC100128885
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6136259copy number variation1nstd213human GRCh37 chr7: 63,890,000-64,210,001 , GRCh38.p12 chr7: 64,429,622-64,749,623 LOC641746, LOC644387, 14 more genes
    nsv6136196copy number variation1nstd213human GRCh37 chr7: 62,900,000-64,980,001 , GRCh38.p12 chr7: 63,439,622-65,515,088 , ZNF138, 95 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5239145copy number variation1nstd204human GRCh38.p13 chr7: 64,574,901-64,581,000 , GRCh37.p13 chr7: 64,035,279-64,041,378 LOC641746, LOC100128885
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
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