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Items: 1 to 20 of 253

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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
    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
    nsv7074748inversion1nstd229human GRCh38 chr8: 22,106,731-22,129,983 , GRCh37.p13 chr8: 21,964,242-21,987,496 NUDT18, HR
    nsv7064256inversion1nstd229human GRCh38 chr8: 22,109,607-22,112,995 , GRCh37.p13 chr8: 21,967,120-21,970,508 HR, NUDT18
    nsv6845628copy number variation1nstd229human GRCh38 chr8: 22,116,296-22,139,606 , GRCh37.p13 chr8: 21,973,809-21,997,119 HR, REEP4
    nsv6842532copy number variation1nstd229human GRCh38 chr8: 21,982,501-22,396,600 , GRCh37.p13 chr8: 21,840,012-22,254,113 SFTPC, BMP1, 16 more genes
    nsv6842345copy number variation1nstd229human GRCh38 chr8: 21,739,201-22,308,765 , GRCh37.p13 chr8: 21,596,713-22,166,278 FHIP2B, FGF17, 17 more genes
    nsv6838774copy number variation1nstd229human GRCh38 chr8: 22,114,687-22,125,522 , GRCh37.p13 chr8: 21,972,200-21,983,035 HR
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6632799copy number variation1nstd224human GRCh37 chr8: 21,975,006-21,986,850 , GRCh38.p12 chr8: 22,117,493-22,129,337 HR
    nsv6555695inversion1nstd223human GRCh38 chr8: 22,106,730-22,129,983 , GRCh37.p13 chr8: 21,964,241-21,987,496 NUDT18, HR
    nsv6435004copy number variation1nstd223human GRCh38 chr8: 22,114,687-22,125,521 , GRCh37.p13 chr8: 21,972,200-21,983,034 HR
    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
    nsv6313650copy number variation1nstd102humanUncertain significance GRCh37 chr8: 21,303,187-22,230,498 , GRCh38.p12 chr8: 21,445,676-22,372,985 OR6R2P, FGF17, 19 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
    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
    nsv6136658copy number variation1nstd213human GRCh37 chr8: 21,490,000-22,700,001 , GRCh38.p12 chr8: 21,632,489-22,842,488 POLR3D, PHYHIP, 37 more genes
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