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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5906982copy number variation1nstd209human GRCh38 chr4: 189,959,873-189,959,953 , GRCh37.p13 chr4|NW_003571034.1: 52,803-52,883 FRG1
    nsv5637028insertion1nstd207human GRCh38 chr4: 189,940,934-189,940,934 , GRCh37.p13 chr4|NW_003571034.1: 33,864-33,864 FRG1, FRG1-DT
    nsv5581382copy number variation1nstd207human GRCh38 chr4: 189,959,894-189,959,960 , GRCh37.p13 chr4|NW_003571034.1: 52,824-52,890 FRG1
    nsv5473534copy number variation1nstd206human GRCh38 chr4: 189,962,514-190,011,200 , GRCh37.p13 chr4|NW_003571034.1: 55,444-104,130 , GRCh37.p13 chr4: 190,897,543-190,932,355 TUBB7P, FRG1, 1 more genes
    nsv5453992copy number variation1nstd206human GRCh38 chr4: 189,925,929-189,944,653 , GRCh37.p13 chr4|NW_003571034.1: 18,859-37,583 FRG1-DT, FRG1
    nsv5301871copy number variation1nstd204human GRCh37.p13 chr4: 190,680,206-190,828,234 , GRCh38.p13 chr4: 189,759,052-190,010,846 FRG1, TUBB7P, 4 more genes
    nsv5233385copy number variation1nstd204human GRCh38.p13 chr4: 189,947,050-189,975,846 , GRCh37.p13 chr4|NW_003571034.1: 39,980-68,776 FRG1, MLLT10P2
    nsv5228147copy number variation1nstd204human GRCh38.p13 chr4: 189,959,012-189,961,127 , GRCh37.p13 chr4|NW_003571034.1: 51,942-54,057 FRG1
    nsv5227215copy number variation1nstd204human GRCh38.p13 chr4: 189,880,401-189,940,200 , GRCh37.p13 chr4|NW_003571034.1: 1-33,130 FRG1-DT, LINC01596, 1 more genes
    nsv5225713copy number variation1nstd204human GRCh38.p13 chr4: 189,937,458-189,968,962 , GRCh37.p13 chr4|NW_003571034.1: 30,388-61,892 FRG1, FRG1-DT
    nsv5220889copy number variation1nstd204human GRCh38.p13 chr4: 189,918,422-189,961,002 , GRCh37.p13 chr4|NW_003571034.1: 11,352-53,932 FRG1-DT, FRG1
    nsv5200366copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 179,554,876-190,916,678 , GRCh38.p12 chr4: 178,633,722-189,995,523 SLC25A4, CASP3, 151 more genes
    nsv4944214copy number variation1nstd200human GRCh38 chr4: 189,899,786-189,993,577 , GRCh37.p13 chr4|NW_003571034.1: 1-86,507 FRG1, FRG1-DT, 2 more genes
    nsv4936668copy number variation1nstd200human GRCh38 chr4: 189,949,481-189,970,602 , GRCh37.p13 chr4|NW_003571034.1: 42,411-63,532 FRG1
    nsv4808390copy number variation1nstd200human GRCh37 chr4: 190,870,636-190,891,757 , GRCh38.p12 chr4: 189,949,481-189,970,602 FRG1
    nsv4794795copy number variation1nstd200human GRCh37 chr4: 190,820,941-190,914,732 , GRCh38.p12 chr4: 189,899,786-189,993,577 MLLT10P2, FRG1, 2 more genes
    nsv4794794copy number variation1nstd200human GRCh37 chr4: 190,803,986-190,913,711 , GRCh38.p12 chr4: 189,882,831-189,992,556 FRG1-DT, TUBB7P, 3 more genes
    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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