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Items: 1 to 20 of 161

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5911209copy number variation1nstd209human GRCh38 chr12: 18,082,971-18,083,144 , GRCh37.p13 chr12: 18,235,905-18,236,078 RERGL
    nsv5561881inversion1nstd206human GRCh38 chr12: 18,069,234-18,081,306 , GRCh37.p13 chr12: 18,222,168-18,234,240 RERGL
    nsv5498881copy number variation1nstd206human GRCh38 chr12: 18,082,971-18,083,145 , GRCh37.p13 chr12: 18,235,905-18,236,079 RERGL
    nsv5327912inversion1nstd204human GRCh38.p13 chr12: 18,069,254-18,081,286 , GRCh37.p13 chr12: 18,222,188-18,234,220 RERGL
    nsv5323122inversion1nstd204human GRCh37.p13 chr12: 6,338,815-22,046,498 , GRCh38.p13 chr12: 6,229,649-21,893,564 , A2M, 414 more genes
    nsv5036517inversion1nstd200human GRCh38 chr12: 18,069,284-18,081,306 , GRCh37.p13 chr12: 18,222,218-18,234,240 RERGL
    nsv4981397copy number variation1nstd200human GRCh38 chr12: 18,077,979-18,093,206 , GRCh37.p13 chr12: 18,230,913-18,246,140 RERGL
    nsv4981396copy number variation1nstd200human GRCh38 chr12: 18,070,860-18,165,234 , GRCh37.p13 chr12: 18,223,794-18,318,168 RERGL
    nsv4882300inversion1nstd200human GRCh37 chr12: 6,338,820-22,046,498 , GRCh38.p12 chr12: 6,229,654-21,893,564 , LOC105369686, 414 more genes
    nsv4873442inversion1nstd200human GRCh37 chr12: 18,222,209-18,234,191 , GRCh38.p12 chr12: 18,069,275-18,081,257 RERGL
    nsv4847137copy number variation1nstd200human GRCh37 chr12: 18,223,793-18,318,168 , GRCh38.p12 chr12: 18,070,859-18,165,234 RERGL
    nsv4831113copy number variation1nstd200human GRCh37 chr12: 18,235,905-18,236,079 , GRCh38.p12 chr12: 18,082,971-18,083,145 RERGL
    nsv4675204copy number variation1nstd102humanUncertain significance GRCh37 chr12: 16,885,566-18,472,797 , GRCh38.p12 chr12: 16,732,632-18,319,863 RNU6-837P, TIMM17BP1, 9 more genes
    nsv4674941copy number variation1nstd102humanPathogenic GRCh37 chr12: 274,676-37,869,301 , GRCh38.p12 chr12: 165,510-37,475,499 LOC105376675, ATF7IP, 682 more genes
    nsv4617775copy number variation1nstd183human GRCh37 chr12: 18,224,826-18,316,141 , GRCh38.p12 chr12: 18,071,892-18,163,207 RERGL
    nsv4614462copy number variation1nstd183human GRCh37 chr12: 18,226,700-18,317,052 , GRCh38.p12 chr12: 18,073,766-18,164,118 RERGL
    nsv4613807copy number variation1nstd183human GRCh37 chr12: 18,096,261-18,259,234 , GRCh38.p12 chr12: 17,943,327-18,106,300 RERGL
    nsv4456793copy number variation1nstd102humanPathogenic GRCh37 chr12: 16,141,429-27,733,325 , GRCh38.p12 chr12: 15,988,495-27,580,392 PDE3A, ETFRF1, 133 more genes
    nsv4455458copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-34,496,628 , GRCh38.p12 chr12: 64,620-34,343,693 EMP1, PLBD1-AS1, 684 more genes
    nsv4436324complex substitution1nstd102humanUncertain significance GRCh38.p12 chr12: 9,922,177-18,648,019 , GRCh37 chr12: 10,074,776-18,800,953 ARHGDIB, ART4, 181 more genes
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