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Items: 1 to 20 of 255

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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
    nsv7098732copy number variation1nstd102humanUncertain significance GRCh37 chr8: 17,915,043-20,112,692 , GRCh38.p12 chr8: 18,057,534-20,255,181 LOC107986868, ASAH1-AS1, 31 more genes
    nsv6854106copy number variation1nstd229human GRCh38 chr8: 19,819,538-19,819,701 , GRCh37.p13 chr8: 19,677,049-19,677,212 INTS10
    nsv6851478copy number variation1nstd229human GRCh38 chr8: 19,478,551-19,947,268 , GRCh37.p13 chr8: 19,336,062-19,804,779 LOC107986921, LPL, 4 more genes
    nsv6848473copy number variation1nstd229human GRCh38 chr8: 19,845,101-19,849,800 , GRCh37.p13 chr8: 19,702,612-19,707,311 INTS10
    nsv6846627copy number variation1nstd229human GRCh38 chr8: 19,707,358-20,616,935 , GRCh37.p13 chr8: 19,564,869-20,474,446 RNU6-892P, LOC107986921, 15 more genes
    nsv6846158copy number variation1nstd229human GRCh38 chr8: 19,219,901-20,283,400 , GRCh37.p13 chr8: 19,077,411-20,140,911 LZTS1, LOC100128993, 17 more genes
    nsv6840295copy number variation1nstd229human GRCh38 chr8: 19,800,148-20,071,854 , GRCh37.p13 chr8: 19,657,659-19,929,365 LPL, LOC107986921, 2 more genes
    nsv6838754copy number variation1nstd229human GRCh38 chr8: 19,700,179-19,964,954 , GRCh37.p13 chr8: 19,557,690-19,822,465 LPL, LOC107986921, 4 more genes
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6565562inversion1nstd223human GRCh38 chr8: 19,825,423-19,826,381 , GRCh37.p13 chr8: 19,682,934-19,683,892 INTS10
    nsv6563724inversion1nstd223human GRCh38 chr8: 19,830,964-19,831,552 , GRCh37.p13 chr8: 19,688,475-19,689,063 INTS10
    nsv6425273copy number variation1nstd223human GRCh38 chr8: 19,816,401-19,818,400 , GRCh37.p13 chr8: 19,673,912-19,675,911 INTS10
    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
    nsv6312905copy number variation1nstd102humanUncertain significance GRCh37 chr8: 16,850,399-20,112,692 , GRCh38.p12 chr8: 16,992,890-20,255,181 MICU3, FGF20, 50 more genes
    nsv6304628copy number variation1nstd186human GRCh37 chr8: 19,675,029-19,677,083 , GRCh38.p12 chr8: 19,817,518-19,819,572 INTS10
    nsv6304214copy number variation1nstd186human GRCh37 chr8: 19,675,177-19,675,732 , GRCh38.p12 chr8: 19,817,666-19,818,221 INTS10
    nsv6291384copy number variation1nstd102humanUncertain significance GRCh37 chr8: 19,157,330-19,780,975 , GRCh38.p12 chr8: 19,299,819-19,923,464 LOC107986921, SH2D4A, 5 more genes
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