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Items: 1 to 20 of 365

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5950520insertion1nstd209human GRCh38 chr3: 186,654,334-186,654,334 , GRCh37.p13 chr3: 186,372,123-186,372,123 HRG-AS1
    nsv5835708copy number variation1nstd209human GRCh38 chr3: 186,689,990-186,702,163 , GRCh37.p13 chr3: 186,407,779-186,419,952 HRGP1, HRG-AS1
    nsv5721212mobile element insertion2nstd211human GRCh38 chr3: 186,654,352-186,654,352 , GRCh37.p13 chr3: 186,372,141-186,372,141 HRG-AS1
    nsv5692382mobile element insertion1nstd211human GRCh38 chr3: 186,654,334-186,654,334 , GRCh37.p13 chr3: 186,372,123-186,372,123 HRG-AS1
    nsv5624004insertion1nstd207human GRCh38 chr3: 186,714,218-186,714,218 , GRCh37.p13 chr3: 186,432,007-186,432,007 HRG-AS1
    nsv5607759insertion1nstd207human GRCh38 chr3: 186,654,334-186,654,334 , GRCh37.p13 chr3: 186,372,123-186,372,123 HRG-AS1
    nsv5557819mobile element insertion1nstd206human GRCh38 chr3: 186,654,352-186,654,403 , GRCh37.p13 chr3: 186,372,141-186,372,192 HRG-AS1
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5453629copy number variation1nstd206human GRCh38 chr3: 186,689,574-186,702,000 , GRCh37.p13 chr3: 186,407,363-186,419,789 HRG-AS1, HRGP1
    nsv5449767copy number variation1nstd206human GRCh38 chr3: 186,668,731-186,706,833 , GRCh37.p13 chr3: 186,386,520-186,424,622 HRG, HRG-AS1, 1 more genes
    nsv5367240translocation1nstd200human GRCh38 chr8: 115,383,576-115,383,576 , GRCh38 chr3: 186,656,488-186,656,488 , GRCh37.p13 chr3: 186,374,277-186,374,277 , GRCh37.p13 chr8: 116,395,805-116,395,805 HRG-AS1
    nsv5367239translocation1nstd200human GRCh38 chr18: 67,403,104-67,403,104 , GRCh38 chr3: 186,656,488-186,656,488 , GRCh37.p13 chr3: 186,374,277-186,374,277 , GRCh37.p13 chr18: 65,070,341-65,070,341 HRG-AS1
    nsv5352302translocation1nstd200human GRCh38 chr3: 186,706,833-186,706,833 , GRCh38 chr3: 186,668,731-186,668,731 , GRCh37.p13 chr3: 186,424,622-186,424,622 , GRCh37.p13 chr3: 186,386,520-186,386,520 HRG, HRG-AS1
    nsv5239574copy number variation1nstd204human GRCh38.p13 chr3: 186,689,147-186,702,207 , GRCh37.p13 chr3: 186,406,936-186,419,996 HRGP1, HRG-AS1
    nsv5235205copy number variation1nstd204human GRCh38.p13 chr3: 186,690,001-186,702,100 , GRCh37.p13 chr3: 186,407,790-186,419,889 HRGP1, HRG-AS1
    nsv5222931copy number variation1nstd204human GRCh38.p13 chr3: 186,691,901-186,702,300 , GRCh37.p13 chr3: 186,409,690-186,420,089 HRG-AS1, HRGP1
    nsv5178984mobile element insertion1nstd203human GRCh38 chr3: 186,654,334-186,654,352 , GRCh37.p13 chr3: 186,372,123-186,372,141 HRG-AS1
    nsv5176200mobile element insertion1nstd203human GRCh38 chr3: 186,654,338-186,654,352 , GRCh37.p13 chr3: 186,372,127-186,372,141 HRG-AS1
    nsv5175465mobile element insertion1nstd203human GRCh38 chr3: 186,654,341-186,654,352 , GRCh37.p13 chr3: 186,372,130-186,372,141 HRG-AS1
    nsv5171252mobile element insertion1nstd203human GRCh38 chr3: 186,654,336-186,654,352 , GRCh37.p13 chr3: 186,372,125-186,372,141 HRG-AS1
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