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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148253copy number variation1nstd102humanPathogenic GRCh38 chr8: 449,893-23,854,904 , GRCh37.p13 chr8: 399,893-23,712,417 ENTPD4, LOC100421446, 447 more genes
    nsv7148146copy number variation1nstd102humanPathogenic GRCh38 chr8: 12,721,809-30,183,737 , GRCh37.p13 chr8: 12,579,318-30,041,253 LOC101929028, RPL35P6, 274 more genes
    nsv7142833insertion1nstd232human GRCh37.p13 chr8: 22,443,148-22,443,148 , GRCh38.p12 chr8: 22,585,635-22,585,635 PDLIM2
    nsv7098901copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 21,925,038-26,372,195 , GRCh38.p12 chr8: 22,067,527-26,514,679 BMP1, POLR3D, 95 more genes
    nsv6851686copy number variation1nstd229human GRCh38 chr8: 22,596,378-22,598,804 , GRCh37.p13 chr8: 22,453,891-22,456,317 C8orf58, PDLIM2
    nsv6850618copy number variation1nstd229human GRCh38 chr8: 22,576,177-22,579,513 , GRCh37.p13 chr8: 22,433,690-22,437,026 SORBS3, PDLIM2
    nsv6845836copy number variation1nstd229human GRCh38 chr8: 22,583,801-22,742,400 , GRCh37.p13 chr8: 22,441,314-22,599,913 PEBP4, LOC105379321, 10 more genes
    nsv6843493copy number variation1nstd229human GRCh38 chr8: 22,589,085-22,589,147 , GRCh37.p13 chr8: 22,446,598-22,446,660 PDLIM2
    nsv6839467copy number variation1nstd229human GRCh38 chr8: 22,579,858-22,579,887 , GRCh37.p13 chr8: 22,437,371-22,437,400 PDLIM2
    nsv6838167copy number variation1nstd229human GRCh38 chr8: 22,575,505-22,576,908 , GRCh37.p13 chr8: 22,433,018-22,434,421 SORBS3, PDLIM2
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6420740copy number variation1nstd223human GRCh38 chr8: 22,596,376-22,598,801 , GRCh37.p13 chr8: 22,453,889-22,456,314 PDLIM2, C8orf58
    nsv6420300copy number variation1nstd223human GRCh38 chr8: 22,531,188-22,580,597 , GRCh37.p13 chr8: 22,388,701-22,438,110 PPP3CC, PDLIM2, 1 more genes
    nsv6315449copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-30,187,456 , GRCh38.p12 chr8: 208,048-30,329,940 LOC101928016, RPL23AP54, 568 more genes
    nsv6315323complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,164,161 , GRCh37 chr8: 158,048-43,019,304 NAT1, NAT2, 760 more genes
    nsv6315176copy number variation1nstd102humanPathogenic GRCh37 chr8: 19,779,604-26,531,980 , GRCh38.p12 chr8: 19,922,093-26,674,463 TNFRSF10C, TNFRSF10A, 121 more genes
    nsv6312718copy number variation2nstd102humanUncertain significance GRCh37 chr8: 21,900,440-23,564,111 , GRCh38.p12 chr8: 22,042,929-23,706,598 LOC105379327, RPL23AP55, 56 more genes
    nsv6269181copy number variation1nstd214human GRCh38 chr8: 22,589,093-22,589,154 , GRCh37.p13 chr8: 22,446,606-22,446,667 PDLIM2
    nsv6265822copy number variation1nstd214human GRCh38 chr8: 22,589,085-22,589,146 , GRCh37.p13 chr8: 22,446,598-22,446,659 PDLIM2
    nsv6137044copy number variation1nstd213human GRCh37 chr8: 12,460,000-33,310,001 , GRCh38.p12 chr8: 12,602,491-33,452,483 NAT1, ASAH1, 322 more genes
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