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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5955580insertion1nstd209human GRCh38 chr8: 143,981,861-143,981,861 , GRCh37.p13 chr8|NW_003315923.1: 320,506-320,506 , GRCh37.p13 chr8: 145,056,029-145,056,029 PARP10
    nsv5632015insertion1nstd207human GRCh38 chr8: 143,981,672-143,981,672 , GRCh37.p13 chr8|NW_003315923.1: 320,317-320,317 , GRCh37.p13 chr8: 145,055,840-145,055,840 PARP10
    nsv5631605insertion1nstd207human GRCh38 chr8: 143,981,916-143,981,916 , GRCh37.p13 chr8|NW_003315923.1: 320,561-320,561 , GRCh37.p13 chr8: 145,056,084-145,056,084 PARP10
    nsv5631471insertion1nstd207human GRCh38 chr8: 143,981,307-143,981,307 , GRCh37.p13 chr8|NW_003315923.1: 319,952-319,952 , GRCh37.p13 chr8: 145,055,475-145,055,475 PARP10
    nsv5630813insertion2nstd207human GRCh38 chr8: 143,981,315-143,981,315 , GRCh37.p13 chr8: 145,055,483-145,055,483 , GRCh37.p13 chr8|NW_003315923.1: 319,960-319,960 PARP10
    nsv5629334insertion1nstd207human GRCh38 chr8: 143,981,512-143,981,512 , GRCh37.p13 chr8|NW_003315923.1: 320,157-320,157 , GRCh37.p13 chr8: 145,055,680-145,055,680 PARP10
    nsv5628705insertion2nstd207human GRCh38 chr8: 143,981,912-143,981,912 , GRCh37.p13 chr8|NW_003315923.1: 320,557-320,557 , GRCh37.p13 chr8: 145,056,080-145,056,080 PARP10
    nsv5627179insertion1nstd207human GRCh38 chr8: 143,981,820-143,981,820 , GRCh37.p13 chr8: 145,055,988-145,055,988 , GRCh37.p13 chr8|NW_003315923.1: 320,465-320,465 PARP10
    nsv5488374copy number variation1nstd206human GRCh38 chr8: 143,981,554-143,981,866 , GRCh37.p13 chr8|NW_003315923.1: 320,199-320,511 , GRCh37.p13 chr8: 145,055,722-145,056,034 PARP10
    nsv5487207copy number variation1nstd206human GRCh38 chr8: 143,981,256-143,981,343 , GRCh37.p13 chr8|NW_003315923.1: 319,901-319,988 , GRCh37.p13 chr8: 145,055,424-145,055,511 PARP10
    nsv5381643copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,047,561-145,701,149 , GRCh38.p12 chr8: 143,973,393-144,475,766 ZFTRAF1, DGAT1, 40 more genes
    nsv5254005copy number variation1nstd204human GRCh37.p13 chr8|NW_003315923.1: 217,346-360,345 , GRCh37.p13 chr8: 144,952,869-145,091,981 , GRCh38.p13 chr8: 143,878,701-144,021,700 GRINA, PLEC, 4 more genes
    nsv5248548copy number variation1nstd204human GRCh38.p13 chr8: 143,866,301-144,531,400 , GRCh37.p13 chr8: 145,146,063-145,756,784 MIR661, EXOSC4, 51 more genes
    nsv4969163copy number variation1nstd200human GRCh38 chr8: 143,982,573-143,984,145 , GRCh37.p13 chr8|NW_003315923.1: 321,218-322,790 , GRCh37.p13 chr8: 145,056,741-145,058,313 PARP10
    nsv4962673copy number variation1nstd200human GRCh38 chr8: 143,980,113-143,982,217 , GRCh37.p13 chr8|NW_003315923.1: 318,758-320,862 , GRCh37.p13 chr8: 145,054,281-145,056,385 PARP10
    nsv4769373copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,033,244-146,297,937 , GRCh38.p12 chr8: 143,959,076-145,072,551 ZFTRAF1, PLEC, 68 more genes
    nsv4760465insertion1nstd199human GRCh37 chr8: 145,055,959-145,055,959 , GRCh38.p12 chr8: 143,981,791-143,981,791 PARP10
    nsv4743907copy number variation1nstd199human GRCh37 chr8: 145,055,959-145,056,536 , GRCh38.p12 chr8: 143,981,791-143,982,368 PARP10
    nsv4729603copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 144,262,042-146,295,771 , GRCh38.p12 chr8: 143,180,625-145,070,385 CYC1, EEF1D, 112 more genes
    nsv4675664copy number variation1nstd102humanPathogenic GRCh37 chr8: 128,877,995-146,295,771 , GRCh38.p12 chr8: 127,865,749-145,070,385 LOC105375789, LINC02990, 270 more genes
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