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Items: 1 to 20 of 164

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5842249copy number variation1nstd209human GRCh38 chr5: 180,853,070-180,902,121 , GRCh37.p13 chr5: 180,280,070-180,329,121 BTNL8, ZFP62
    nsv5841959copy number variation1nstd209human GRCh38 chr5: 180,861,134-180,869,254 , GRCh37.p13 chr5: 180,288,134-180,296,254 ZFP62
    nsv5841958copy number variation1nstd209human GRCh38 chr5: 180,825,213-180,874,088 , GRCh37.p13 chr5: 180,252,213-180,301,088 , ZFP62, 2 more genes
    nsv4949317copy number variation1nstd200human GRCh38 chr5: 180,849,782-181,061,634 , GRCh37.p13 chr5: 180,276,782-180,488,634 RPS29P12, ZFP62, 8 more genes
    nsv4940225copy number variation1nstd200human GRCh38 chr5: 180,849,983-180,858,522 , GRCh37.p13 chr5: 180,276,983-180,285,522 ZFP62
    nsv4828428copy number variation1nstd200human GRCh37 chr5: 180,276,782-180,488,634 , GRCh38.p12 chr5: 180,849,782-181,061,634 RPS29P12, ZFP62, 8 more genes
    nsv4768375copy number variation1nstd102humanPathogenic GRCh37 chr5: 170,805,664-180,719,789 , GRCh38.p12 chr5: 171,378,660-181,292,788 LINC01863, PRDX2P3, 279 more genes
    nsv4728969copy number variation1nstd102humanUncertain significance GRCh37 chr5: 180,064,955-180,719,789 , GRCh38.p12 chr5: 180,637,955-181,292,788 TMEM69P2, OR2V1, 52 more genes
    nsv4675982copy number variation1nstd102humanUncertain significance GRCh37 chr5: 180,277,974-180,579,560 , GRCh38.p12 chr5: 180,850,974-181,152,560 BTNL3, BTNL8, 16 more genes
    nsv4675130copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,487,249-180,622,216 , GRCh38.p12 chr5: 179,060,248-181,195,216 OR2V2, TRV-AAC1-2, 81 more genes
    nsv4675041copy number variation1nstd102humanUncertain significance GRCh37 chr5: 179,479,838-180,695,063 , GRCh38.p12 chr5: 180,052,838-181,268,062 OR2AI1P, SNORD96A, 64 more genes
    nsv4674857copy number variation1nstd102humanLikely benign GRCh37 chr5: 180,277,974-180,491,461 , GRCh38.p12 chr5: 180,850,974-181,064,461 RNU6-1036P, BTNL8, 9 more genes
    nsv4592961copy number variation1nstd183human GRCh37 chr5: 180,287,553-180,288,219 , GRCh38.p12 chr5: 180,860,553-180,861,219 ZFP62
    nsv4590824copy number variation1nstd183human GRCh37 chr5: 180,288,174-180,288,219 , GRCh38.p12 chr5: 180,861,174-180,861,219 ZFP62
    nsv4590823copy number variation1nstd183human GRCh37 chr5: 180,261,189-180,279,120 , GRCh38.p12 chr5: 180,834,189-180,852,120 ZFP62, LINC00847
    nsv4482901mobile element insertion1nstd166human GRCh37.p13 chr5: 180,278,850-180,278,850 , GRCh38.p12 chr5: 180,851,850-180,851,850 ZFP62
    nsv4455497copy number variation1nstd102humanPathogenic GRCh37 chr5: 176,848,982-180,719,789 , GRCh38.p12 chr5: 177,421,981-181,292,788 HEIH, MGAT4B, 149 more genes
    nsv4350559copy number variation1nstd102humanPathogenic GRCh37 chr5: 174,990,352-180,690,937 , GRCh38.p12 chr5: 175,563,349-181,263,936 FAF2, ARL10, 198 more genes
    nsv4350315copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 177,776,148-180,687,012 , GRCh38.p12 chr5: 178,349,147-181,260,011 CANX, FOXO1B, 114 more genes
    nsv4347913copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 175,843,728-180,703,728 , GRCh38.p12 chr5: 176,416,727-181,276,727 CANX, CLTB, 177 more genes
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