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Items: 1 to 20 of 307

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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
    nsv7148131copy number variation1nstd102humanPathogenic GRCh37 chr8: 10,501-11,142,629 , GRCh38.p12 chr8: 60,501-11,285,120 XKR6, FAM90A11, 224 more genes
    nsv7072551inversion1nstd229human GRCh38 chr8: 7,050,286-7,059,902 , GRCh37.p13 chr8: 6,907,808-6,917,424 DEFA5
    nsv7071705inversion1nstd229human GRCh38 chr8: 7,041,770-8,576,733 , GRCh37.p13 chr8: 6,899,292-8,434,243 FAM90A7, SNRPCP15, 86 more genes
    nsv7068583inversion1nstd229human GRCh38 chr8: 6,839,737-7,068,121 , GRCh37.p13 chr8: 6,697,259-6,925,643 DEFA1B, DEFA7P, 14 more genes
    nsv6843340copy number variation1nstd229human GRCh38 chr8: 7,049,425-7,056,065 , GRCh37.p13 chr8: 6,906,947-6,913,587 DEFA5
    nsv6636968copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,049-18,936,715 , GRCh38.p12 chr8: 208,049-19,079,205 ZNF705B, NATP, 357 more genes
    nsv6636940copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,049-10,965,627 , GRCh38.p12 chr8|NW_018654717.1: 1-5,513,617 , GRCh38.p12 chr8: 208,049-11,108,117 HSPD1P3, LOC401442, 270 more genes
    nsv6636325copy number variation1nstd102humanUncertain significance GRCh37 chr8: 6,284,373-9,047,178 , GRCh38.p12 chr8: 6,426,852-9,189,668 DEFB105B, LOC105379216, 127 more genes
    nsv6634376copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-11,281,408 , GRCh38.p12 chr8: 208,048-11,423,899 DLGAP2-AS1, MIR124-1HG, 228 more genes
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6633101copy number variation1nstd224human GRCh37 chr8: 6,901,373-7,210,533 , GRCh38.p12 chr8: 7,043,851-7,353,011 FAM90A3, FAM90A15, 21 more genes
    nsv6632901copy number variation1nstd224human GRCh37 chr8: 6,879,803-7,216,072 , GRCh38.p12 chr8: 7,022,281-7,358,550 LOC402329, FAM90A13, 24 more genes
    nsv6632826copy number variation1nstd224human GRCh37 chr8: 6,635,957-7,003,534 , GRCh38.p12 chr8: 6,778,436-7,146,012 , GRCh38.p12 chr8|NW_018654717.1: 173,708-541,171 DEFA1, DEFA5, 22 more genes
    nsv6432648copy number variation1nstd223human GRCh38 chr8: 7,054,473-7,059,358 , GRCh37.p13 chr8: 6,911,995-6,916,880 DEFA5
    nsv6315449copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-30,187,456 , GRCh38.p12 chr8: 208,048-30,329,940 LOC101928016, RPL23AP54, 568 more genes
    nsv6315342copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-10,348,413 , GRCh38.p12 chr8|NW_018654717.1: 1-5,513,617 , GRCh38.p12 chr8: 208,048-10,490,903 MIR1322, MIR548I3, 269 more genes
    nsv6315323complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,164,161 , GRCh37 chr8: 158,048-43,019,304 NAT1, NAT2, 760 more genes
    nsv6290796copy number variation1nstd102humanLikely benign GRCh37 chr8: 6,904,643-6,999,114 , GRCh38.p12 chr8: 7,047,121-7,141,592 , GRCh38.p12 chr8|NW_018654717.1: 442,246-536,749 DEFA5, RPS3AP30, 5 more genes
    nsv6290739copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-11,936,107 , GRCh38.p12 chr8: 208,048-12,078,598 DLGAP2-AS1, FAM86B3P, 254 more genes
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