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Items: 1 to 20 of 165

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131043insertion1nstd186human GRCh37 chr15: 63,438,480-63,438,500 , GRCh38.p12 chr15: 63,146,281-63,146,301 RPS27L
    nsv5975502insertion1nstd209human GRCh38 chr15: 63,146,250-63,146,250 , GRCh37.p13 chr15: 63,438,449-63,438,449 RPS27L
    nsv5703910mobile element insertion1nstd211human GRCh38 chr15: 63,149,601-63,149,601 , GRCh37.p13 chr15: 63,441,800-63,441,800 RPS27L
    nsv5658582insertion1nstd207human GRCh38 chr15: 63,146,250-63,146,250 , GRCh37.p13 chr15: 63,438,449-63,438,449 RPS27L
    nsv5586014copy number variation1nstd207human GRCh38 chr15: 63,149,543-63,149,619 , GRCh37.p13 chr15: 63,441,742-63,441,818 RPS27L
    nsv5538320insertion1nstd206human GRCh38 chr15: 63,146,281-63,146,301 , GRCh37.p13 chr15: 63,438,480-63,438,500 RPS27L
    nsv5533038copy number variation1nstd206human GRCh38 chr15: 63,087,669-63,253,345 , GRCh37.p13 chr15: 63,379,868-63,545,544 LOC107984798, RAB8B, 3 more genes
    nsv5522826copy number variation1nstd206human GRCh38 chr15: 63,149,543-63,149,620 , GRCh37.p13 chr15: 63,441,742-63,441,819 RPS27L
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5357998translocation1nstd200human GRCh38 chr15: 63,149,543-63,149,543 , GRCh38 chr15: 63,149,620-63,149,620 , GRCh37.p13 chr15: 63,441,742-63,441,742 , GRCh37.p13 chr15: 63,441,819-63,441,819 RPS27L
    nsv5338941translocation1nstd200human GRCh37 chr15: 63,441,742-63,441,742 , GRCh37 chr15: 63,441,819-63,441,819 , GRCh38.p12 chr15: 63,149,620-63,149,620 , GRCh38.p12 chr15: 63,149,543-63,149,543 RPS27L
    nsv5320565translocation1nstd204human GRCh38.p13 chr15: 63,149,543-63,149,543 , GRCh38.p13 chr15: 63,149,620-63,149,620 , GRCh37.p13 chr15: 63,441,819-63,441,819 , GRCh37.p13 chr15: 63,441,742-63,441,742 RPS27L
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv5005493copy number variation1nstd200human GRCh38 chr15: 63,143,611-63,157,730 , GRCh37.p13 chr15: 63,435,810-63,449,929 RPS27L
    nsv4991951copy number variation1nstd200human GRCh38 chr15: 63,148,914-63,150,666 , GRCh37.p13 chr15: 63,441,113-63,442,865 RPS27L
    nsv4872280inversion1nstd200human GRCh37 chr15: 40,414,149-64,343,008 , GRCh38.p12 chr15: 40,121,948-64,050,809 , DNAAF4-CCPG1, 475 more genes
    nsv4863844copy number variation1nstd200human GRCh37 chr15: 63,435,710-63,450,061 , GRCh38.p12 chr15: 63,143,511-63,157,862 RPS27L
    nsv4747837copy number variation1nstd199human GRCh37 chr15: 63,441,742-63,441,818 , GRCh38.p12 chr15: 63,149,543-63,149,619 RPS27L
    nsv4721199insertion1nstd186human GRCh37 chr15: 63,438,449-63,438,449 , GRCh38.p12 chr15: 63,146,250-63,146,250 RPS27L
    nsv4682962copy number variation1nstd102humanUncertain significance GRCh37 chr15: 63,335,019-64,161,352 , GRCh38.p12 chr15: 63,042,820-63,869,153 LOC107984798, LOC101928972, 13 more genes
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