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Items: 1 to 20 of 211

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5899068copy number variation1nstd209human GRCh38 chr4: 56,359,545-56,359,841 , GRCh37.p13 chr4: 57,225,711-57,226,007 AASDH
    nsv5725791mobile element insertion1nstd211human GRCh38 chr4: 56,338,155-56,338,155 , GRCh37.p13 chr4: 57,204,321-57,204,321 AASDH
    nsv5674237copy number variation1nstd102humanPathogenic GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872 FTLP10, RNU6-410P, 335 more genes
    nsv5562695mobile element insertion1nstd206human GRCh38 chr4: 56,338,155-56,338,206 , GRCh37.p13 chr4: 57,204,321-57,204,372 AASDH
    nsv5557875sequence alteration1nstd206human GRCh38 chr4: 56,179,761-56,589,194 , GRCh37.p13 chr4: 57,045,927-57,455,360 , PPAT, 12 more genes
    nsv5459616copy number variation1nstd206human GRCh38 chr4: 56,377,000-56,386,000 , GRCh37.p13 chr4: 57,243,166-57,252,166 AASDH
    nsv5211949mobile element deletion1nstd204human GRCh38.p13 chr4: 56,359,553-56,359,847 , GRCh37.p13 chr4: 57,225,719-57,226,013 AASDH
    nsv5097109mobile element insertion1nstd203human GRCh38 chr4: 56,346,879-56,346,894 , GRCh37.p13 chr4: 57,213,045-57,213,060 AASDH
    nsv5087171mobile element insertion1nstd203human GRCh38 chr4: 56,339,588-56,339,604 , GRCh37.p13 chr4: 57,205,754-57,205,770 AASDH
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 more genes
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4928808copy number variation1nstd200human GRCh38 chr4: 56,370,566-56,370,693 , GRCh37.p13 chr4: 57,236,732-57,236,859 AASDH
    nsv4928805copy number variation1nstd200human GRCh38 chr4: 56,213,754-56,393,163 , GRCh37.p13 chr4: 57,079,920-57,259,329 , PPAT, 7 more genes
    nsv4925633copy number variation1nstd200human GRCh38 chr4: 56,371,672-56,373,544 , GRCh37.p13 chr4: 57,237,838-57,239,710 AASDH
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
    nsv4874857mobile element deletion1nstd200human GRCh38 chr4: 56,359,559-56,359,842 , GRCh37.p13 chr4: 57,225,725-57,226,008 AASDH
    nsv4778057mobile element deletion1nstd200human GRCh37 chr4: 57,225,725-57,226,008 , GRCh38.p12 chr4: 56,359,559-56,359,842 AASDH
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 more genes
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