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Items: 1 to 20 of 274

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5492134copy number variation1nstd206human GRCh38 chr8: 615,928-1,447,488 , GRCh37.p13 chr8: 565,928-1,395,654 , DLGAP2, 7 more genes
    nsv5303859copy number variation1nstd204human GRCh38.p13 chr8: 634,570-1,043,257 , GRCh37.p13 chr8: 584,570-993,257 , DLGAP2, 3 more genes
    nsv5241479copy number variation1nstd204human GRCh38.p13 chr8: 676,501-990,400 , GRCh37.p13 chr8: 626,501-940,400 , DLGAP2, 3 more genes
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv4968959copy number variation1nstd200human GRCh38 chr8: 637,927-882,906 , GRCh37.p13 chr8: 587,927-832,906 , LOC105377777, 3 more genes
    nsv4968956copy number variation1nstd200human GRCh38 chr8: 584,483-774,848 , GRCh37.p13 chr8: 534,483-724,848 ERICH1, DLGAP2, 1 more genes
    nsv4968952copy number variation1nstd200human GRCh38 chr8: 476,298-808,142 , GRCh37.p13 chr8: 426,298-758,142 FBXO25, LOC401442, 3 more genes
    nsv4968951copy number variation1nstd200human GRCh38 chr8: 444,159-766,693 , GRCh37.p13 chr8: 394,159-716,693 ERICH1, DLGAP2, 3 more genes
    nsv4825524copy number variation1nstd200human GRCh37 chr8: 587,927-832,906 , GRCh38.p12 chr8|NT_187572.1: 1-145,606 , GRCh38.p12 chr8: 637,927-882,906 , ERICH1, 3 more genes
    nsv4729501copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-3,476,104 , GRCh38.p12 chr8: 208,048-3,618,582 LOC105377782, ZNF596, 37 more genes
    nsv4729425copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-1,411,510 , GRCh38.p12 chr8: 208,048-1,463,344 ZNF596, RPL23AP53, 13 more genes
    nsv4729256copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-2,081,207 , GRCh38.p12 chr8: 208,048-2,017,223 LOC105377778, LOC286083, 26 more genes
    nsv4729120copy number variation1nstd102humanPathogenic GRCh37 chr8: 411,691-6,999,114 , GRCh38.p12 chr8: 461,691-7,141,592 LOC105377795, AGPAT5, 81 more genes
    nsv4685988copy number variation1nstd102humanPathogenic GRCh37 chr8: 161,516-11,516,619 , GRCh38.p12 chr8: 211,516-11,659,110 ZNF705B, RNU6-682P, 232 more genes
    nsv4675925copy number variation1nstd102humanLikely benign GRCh37 chr8: 541,616-853,721 , GRCh38.p12 chr8: 591,616-903,721 ERICH1, DLGAP2, 2 more genes
    nsv4675804copy number variation1nstd102humanLikely benign GRCh37 chr8: 639,795-1,275,384 , GRCh38.p12 chr8: 689,795-1,327,218 ERICH1, DLGAP2, 3 more genes
    nsv4675777copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-9,025,197 , GRCh38.p12 chr8: 208,048-9,167,687 FAM87A, LOC100131395, 182 more genes
    nsv4675668copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-4,188,901 , GRCh38.p12 chr8: 208,048-4,331,379 MIR3674, LOC105377775, 39 more genes
    nsv4675494copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-8,102,819 , GRCh38.p12 chr8: 208,048-8,245,297 HSPD1P3, LOC105377791, 164 more genes
    nsv4675295copy number variation1nstd102humanLikely benign GRCh37 chr8: 158,048-704,967 , GRCh38.p12 chr8: 208,048-754,967 FAM87A, RPL23AP53, 8 more genes
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