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Items: 1 to 20 of 155

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5911215copy number variation1nstd209human GRCh38 chr7: 930,402-2,311,664 , GRCh37.p13 chr7: 970,038-2,351,299 , GPR146, 40 more genes
    nsv5226273copy number variation1nstd204human GRCh37.p13 chr7: 2,278,536-2,407,135 , GRCh38.p13 chr7: 2,238,901-2,367,500 NUDT1, EIF3B, 4 more genes
    nsv4953221copy number variation1nstd200human GRCh38 chr7: 2,219,084-2,297,460 , GRCh37.p13 chr7: 2,258,719-2,337,095 NUDT1, SNX8, 4 more genes
    nsv4953218copy number variation1nstd200human GRCh38 chr7: 2,029,930-2,586,635 , GRCh37.p13 chr7: 2,069,565-2,626,269 , NGRNP3, 18 more genes
    nsv4949586copy number variation1nstd200human GRCh38 chr7: 2,164,456-2,258,444 , GRCh37.p13 chr7: 2,204,091-2,298,079 NUDT1, MAD1L1, 4 more genes
    nsv4949573copy number variation1nstd200human GRCh38 chr7: 1,926,986-2,281,113 , GRCh37.p13 chr7: 1,966,622-2,320,748 NUDT1, MAD1L1, 6 more genes
    nsv4824981copy number variation1nstd200human GRCh37 chr7: 2,268,144-2,353,054 , GRCh38.p12 chr7: 2,228,509-2,313,419 MAD1L1, MIR6836, 4 more genes
    nsv4824980copy number variation1nstd200human GRCh37 chr7: 2,258,719-2,337,095 , GRCh38.p12 chr7: 2,219,084-2,297,460 MAD1L1, IMMP1LP3, 4 more genes
    nsv4824978copy number variation1nstd200human GRCh37 chr7: 2,069,565-2,626,269 , GRCh38.p12 chr7: 2,029,930-2,586,635 , SNORA114, 18 more genes
    nsv4729731copy number variation1nstd102humanUncertain significance GRCh37 chr7: 2,155,103-2,629,996 , GRCh38.p12 chr7: 2,115,468-2,590,362 MAD1L1, LOC105375127, 16 more genes
    nsv4729694copy number variation1nstd102humanUncertain significance GRCh37 chr7: 2,169,252-2,577,781 , GRCh38.p12 chr7: 2,129,617-2,538,147 IMMP1LP3, NGRNP3, 14 more genes
    nsv4729380copy number variation1nstd102humanUncertain significance GRCh37 chr7: 2,082,065-2,669,221 , GRCh38.p12 chr7: 2,042,430-2,629,587 LOC107986760, CHST12, 18 more genes
    nsv4709700copy number variation1nstd195human GRCh37 chr7: 2,202,201-2,307,001 , GRCh38.p12 chr7: 2,162,566-2,267,366 NUDT1, MAD1L1, 4 more genes
    nsv4675817copy number variation1nstd102humanPathogenic GRCh37 chr7: 1,648,373-10,627,513 , GRCh38.p12 chr7: 1,608,737-10,587,886 TTYH3, UNC93B2, 150 more genes
    nsv4604737copy number variation1nstd183human GRCh37 chr7: 2,021,682-2,380,364 , GRCh38.p12 chr7: 1,982,047-2,340,729 NUDT1, MAD1L1, 7 more genes
    nsv4456827copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,376-19,520,619 , GRCh38.p12 chr7: 43,376-19,480,996 MIR6836, EEF1A1P26, 277 more genes
    nsv4456665copy number variation1nstd102humanUncertain significance GRCh37 chr7: 2,214,169-2,380,156 , GRCh38.p12 chr7: 2,174,534-2,340,521 NUDT1, SNX8, 5 more genes
    nsv4456136copy number variation1nstd102humanPathogenic GRCh37 chr7: 36,616-4,298,168 , GRCh38.p12 chr7: 36,616-4,258,536 LOC442497, LFNG, 85 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4393791copy number variation1nstd174human GRCh37 chr7: 2,269,895-2,364,944 , GRCh38.p12 chr7: 2,230,260-2,325,309 NUDT1, MAD1L1, 4 more genes
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