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Items: 1 to 20 of 129

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075962inversion1nstd229human GRCh38 chr12: 99,728,274-100,301,277 , GRCh37.p13 chr12: 100,122,052-100,695,055 DEPDC4, RN7SL176P, 8 more genes
    nsv7074674inversion1nstd229human GRCh38 chr12: 100,072,817-104,989,567 , GRCh37.p13 chr12: 100,466,595-105,383,345 SYCP3, GOLGA2P5, 84 more genes
    nsv7068612inversion1nstd229human GRCh38 chr12: 100,083,131-104,989,539 , GRCh37.p13 chr12: 100,476,909-105,383,317 EID3, RNU6-1068P, 84 more genes
    nsv6935528copy number variation1nstd229human GRCh38 chr12: 100,161,722-100,164,615 , GRCh37.p13 chr12: 100,555,500-100,558,393 GOLGA2P5
    nsv6932882copy number variation1nstd229human GRCh38 chr12: 100,124,100-100,158,017 , GRCh37.p13 chr12: 100,517,878-100,551,795 GOLGA2P5, DNM1P19, 2 more genes
    nsv6932064copy number variation1nstd229human GRCh38 chr12: 100,091,176-100,186,453 , GRCh37.p13 chr12: 100,484,954-100,580,231 RN7SL176P, BLTP3B, 2 more genes
    nsv6931790copy number variation1nstd229human GRCh38 chr12: 100,151,601-100,174,000 , GRCh37.p13 chr12: 100,545,379-100,567,778 GOLGA2P5, DNM1P19, 1 more genes
    nsv6928585copy number variation1nstd229human GRCh38 chr12: 100,148,786-100,155,791 , GRCh37.p13 chr12: 100,542,564-100,549,569 GOLGA2P5, DNM1P19
    nsv6926514copy number variation1nstd229human GRCh38 chr12: 99,947,178-100,328,732 , GRCh37.p13 chr12: 100,340,956-100,722,510 BLTP3B, MIR1827, 8 more genes
    nsv6922635copy number variation1nstd229human GRCh38 chr12: 96,115,345-104,800,221 , GRCh37.p13 chr12: 96,509,123-105,193,999 RNY1P16, CHST11, 121 more genes
    nsv6919967copy number variation1nstd229human GRCh38 chr12: 100,162,096-100,168,047 , GRCh37.p13 chr12: 100,555,874-100,561,825 GOLGA2P5
    nsv6621296copy number variation1nstd224human GRCh37 chr12: 100,451,442-100,631,797 , GRCh38.p12 chr12: 100,057,664-100,238,019 BLTP3B, GOLGA2P5, 5 more genes
    nsv6475315copy number variation1nstd223human GRCh38 chr12: 100,124,100-100,158,010 , GRCh37.p13 chr12: 100,517,878-100,551,788 DNM1P19, GOLGA2P5, 2 more genes
    nsv6465286copy number variation1nstd223human GRCh38 chr12: 100,151,576-100,173,964 , GRCh37.p13 chr12: 100,545,354-100,567,742 RN7SL176P, DNM1P19, 1 more genes
    nsv6463676copy number variation1nstd223human GRCh38 chr12: 100,055,590-100,257,781 , GRCh37.p13 chr12: 100,449,368-100,651,559 MIR1827, RN7SL176P, 5 more genes
    nsv6313913copy number variation1nstd102humanUncertain significance GRCh37 chr12: 100,564,593-103,021,075 , GRCh38.p12 chr12: 100,170,815-102,627,297 DEPDC4, SLC5A8, 46 more genes
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv5505953copy number variation1nstd206human GRCh38 chr12: 100,159,610-100,165,224 , GRCh37.p13 chr12: 100,553,388-100,559,002 GOLGA2P5
    nsv5503809copy number variation1nstd206human GRCh38 chr12: 100,151,576-100,173,964 , GRCh37.p13 chr12: 100,545,354-100,567,742 GOLGA2P5, RN7SL176P, 1 more genes
    nsv5305466copy number variation1nstd204human GRCh38.p13 chr12: 100,159,425-100,165,484 , GRCh37.p13 chr12: 100,553,203-100,559,262 GOLGA2P5
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