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Items: 1 to 20 of 184

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5968065inversion1nstd209human GRCh38 chr3: 14,742,874-15,551,121 , GRCh37.p13 chr3: 14,784,381-15,592,628 , NR2C2, 21 more genes
    nsv5965635insertion1nstd209human GRCh37.p13 chr3: 15,294,326-15,294,326 , GRCh38 chr3: 15,252,819-15,252,819 SH3BP5, CAPN7, 1 more genes
    nsv5692553mobile element insertion2nstd211human GRCh38 chr3: 15,238,873-15,238,873 , GRCh37.p13 chr3: 15,280,380-15,280,380 CAPN7
    nsv5679861mobile element insertion2nstd211human GRCh38 chr3: 15,252,835-15,252,835 , GRCh37.p13 chr3: 15,294,342-15,294,342 SH3BP5, CAPN7, 1 more genes
    nsv5606581insertion1nstd207human GRCh38 chr3: 15,252,826-15,252,826 , GRCh37.p13 chr3: 15,294,333-15,294,333 SH3BP5, CAPN7, 1 more genes
    nsv5559332sequence alteration1nstd206human GRCh38 chr3: 15,253,173-15,254,103 , GRCh37.p13 chr3: 15,294,680-15,295,610 SH3BP5, CAPN7, 1 more genes
    nsv5400038mobile element insertion1nstd206human GRCh38 chr3: 15,252,826-15,252,826 , GRCh37.p13 chr3: 15,294,333-15,294,333 SH3BP5, CAPN7, 1 more genes
    nsv5367004translocation1nstd200human GRCh38 chr3: 15,254,104-15,254,104 , GRCh38 chr3: 15,253,174-15,253,174 , GRCh37.p13 chr3: 15,295,611-15,295,611 , GRCh37.p13 chr3: 15,294,681-15,294,681 SH3BP5, CAPN7, 1 more genes
    nsv5367003translocation1nstd200human GRCh38 chr3: 15,251,665-15,251,665 , GRCh38 chr7: 786,071-786,071 , GRCh37.p13 chr3: 15,293,172-15,293,172 , GRCh37.p13 chr7: 825,708-825,708 CAPN7, DNAAF5
    nsv5367002translocation1nstd200human GRCh38 chr3: 15,251,649-15,251,649 , GRCh38 chr7: 786,475-786,475 , GRCh37.p13 chr3: 15,293,156-15,293,156 , GRCh37.p13 chr7: 826,112-826,112 CAPN7, DNAAF5
    nsv5341446translocation1nstd200human GRCh37 chr3: 15,295,611-15,295,611 , GRCh37 chr3: 15,294,681-15,294,681 , GRCh38.p12 chr3: 15,254,104-15,254,104 , GRCh38.p12 chr3: 15,253,174-15,253,174 SH3BP5, CAPN7, 1 more genes
    nsv5211186copy number variation1nstd204human GRCh38.p13 chr3: 15,228,850-15,230,949 , GRCh37.p13 chr3: 15,270,357-15,272,456 CAPN7
    nsv5079984mobile element insertion1nstd203human GRCh38 chr3: 15,226,376-15,226,386 , GRCh37.p13 chr3: 15,267,883-15,267,893 CAPN7
    nsv5078759mobile element insertion1nstd203human GRCh38 chr3: 15,253,366-15,253,384 , GRCh37.p13 chr3: 15,294,873-15,294,891 SH3BP5, CAPN7, 1 more genes
    nsv5077020mobile element insertion1nstd203human GRCh38 chr3: 15,252,824-15,252,835 , GRCh37.p13 chr3: 15,294,331-15,294,342 SH3BP5, CAPN7, 1 more genes
    nsv5074406mobile element insertion1nstd203human GRCh38 chr3: 15,252,832-15,252,835 , GRCh37.p13 chr3: 15,294,339-15,294,342 SH3BP5, CAPN7, 1 more genes
    nsv5072757mobile element insertion1nstd203human GRCh38 chr3: 15,252,818-15,252,835 , GRCh37.p13 chr3: 15,294,325-15,294,342 SH3BP5, CAPN7, 1 more genes
    nsv5066809mobile element insertion1nstd203human GRCh38 chr3: 15,252,830-15,252,835 , GRCh37.p13 chr3: 15,294,337-15,294,342 SH3BP5, CAPN7, 1 more genes
    nsv5065830mobile element insertion1nstd203human GRCh38 chr3: 15,224,240-15,224,255 , GRCh37.p13 chr3: 15,265,747-15,265,762 CAPN7
    nsv5065122mobile element insertion1nstd203human GRCh38 chr3: 15,252,819-15,252,835 , GRCh37.p13 chr3: 15,294,326-15,294,342 SH3BP5, CAPN7, 1 more genes
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