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Items: 1 to 20 of 111

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5935349copy number variation1nstd209human GRCh38 chr15: 77,970,674-82,312,707 , GRCh37.p13 chr15: 78,263,016-82,605,043 , ST20, 91 more genes
    nsv5601153copy number variation1nstd207human GRCh38 chr15: 81,323,239-81,323,316 , GRCh37.p13 chr15: 81,615,580-81,615,657 STARD5, TMC3-AS1
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5001984copy number variation1nstd200human GRCh38 chr15: 81,319,799-81,319,894 , GRCh37.p13 chr15: 81,612,140-81,612,235 STARD5
    nsv4992298copy number variation1nstd200human GRCh38 chr15: 73,152,590-82,101,178 , GRCh37.p13 chr15: 73,444,931-82,393,519 , SNUPN, 215 more genes
    nsv4733724copy number variation1nstd199human GRCh37 chr15: 81,615,581-81,615,664 , GRCh38.p12 chr15: 81,323,240-81,323,323 TMC3-AS1, STARD5
    nsv4623186copy number variation1nstd183human GRCh37 chr15: 81,550,103-81,636,267 , GRCh38.p12 chr15: 81,257,762-81,343,926 IL16, TMC3, 2 more genes
    nsv4456639copy number variation1nstd102humanPathogenic GRCh37 chr15: 80,728,654-84,107,646 , GRCh38.p12 chr15: 80,436,313-83,438,894 LOC100288241, LOC105370926, 64 more genes
    nsv4447250copy number variation1nstd175human GRCh37 chr15: 81,615,580-81,615,658 , GRCh38.p12 chr15: 81,323,239-81,323,317 STARD5, TMC3-AS1
    nsv4248732copy number variation1nstd166human GRCh37.p13 chr15: 81,615,659-81,616,302 , GRCh38.p12 chr15: 81,323,318-81,323,961 STARD5, TMC3-AS1
    nsv4233111copy number variation1nstd166human GRCh37.p13 chr15: 81,612,140-81,612,235 , GRCh38.p12 chr15: 81,319,799-81,319,894 STARD5
    nsv3935705copy number variation1nstd167human GRCh37 chr15: 81,615,580-81,615,658 , GRCh38.p12 chr15: 81,323,239-81,323,317 STARD5, TMC3-AS1
    nsv3922157copy number variation1nstd102humanUncertain significance NCBI36 chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189 GCHFR, SPPL2A, 1382 more genes
    nsv3919468copy number variation1nstd102humanPathogenic NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189 RNU6-18P, GOLGA8K, 1442 more genes
    nsv3918992copy number variation1nstd102humanPathogenic NCBI36 chr15: 75,141,730-95,931,047 , GRCh37.p13 chr15: 77,354,675-98,130,043 , GRCh38.p12 chr15: 77,062,333-97,586,813 TLNRD1, FES, 403 more genes
    nsv3918770copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,280,728-100,338,915 , GRCh37.p13 chr15: 22,729,364-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNRPCP18, SNORD116-30, 1622 more genes
    nsv3918644copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,313,935-100,338,915 , GRCh37.p13 chr15: 22,762,571-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNORD116-23, UBE2Q2P6, 1622 more genes
    nsv3917589copy number variation1nstd102humanPathogenic GRCh37 chr15: 60,120,659-102,461,201 , GRCh38 chr15: 59,828,460-101,920,998 , NCBI36 chr15: 57,907,951-100,278,724 GAPDHP61, SNORD18B, 840 more genes
    nsv3916249copy number variation1nstd102humanPathogenic NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189 H3P40, EEF1B2P1, 1616 more genes
    nsv3915210copy number variation1nstd102humanUncertain significance NCBI36 chr15: 28,207,117-100,338,915 , GRCh37.p13 chr15: 30,419,825-102,521,392 , GRCh38.p12 chr15: 30,127,622-101,981,189 RPL21P113, LOC112268152, 1428 more genes
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