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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112778copy number variation1nstd102humanPathogenic GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273 LINC01742, MTCO2P1, 253 more genes
    nsv5958911copy number variation1nstd209human GRCh38 chr20: 63,895,321-63,928,331 , GRCh37.p13 chr20: 62,526,674-62,559,684 DNAJC5, MIR941-1, 5 more genes
    nsv5665037insertion1nstd207human GRCh37.p13 chr20: 62,551,216-62,551,216 , GRCh38 chr20: 63,919,863-63,919,863 DNAJC5, MIR941-1, 4 more genes
    nsv5602542copy number variation1nstd207human GRCh37.p13 chr20: 62,551,143-62,551,198 , GRCh38 chr20: 63,919,790-63,919,845 DNAJC5, MIR941-1, 4 more genes
    nsv5593497copy number variation1nstd207human GRCh37.p13 chr20: 62,551,030-62,551,224 , GRCh38 chr20: 63,919,677-63,919,871 DNAJC5, MIR941-1, 4 more genes
    nsv5587639copy number variation1nstd207human GRCh37.p13 chr20: 62,550,791-62,551,014 , GRCh38 chr20: 63,919,438-63,919,661 DNAJC5, MIR941-1, 4 more genes
    nsv5562694sequence alteration1nstd206human GRCh38 chr20: 63,525,502-63,937,515 , GRCh37.p13 chr20: 62,156,855-62,568,868 , STMN3, 26 more genes
    nsv5521119copy number variation1nstd206human GRCh38 chr20: 63,914,834-63,918,778 , GRCh37.p13 chr20: 62,546,187-62,550,131 DNAJC5, MIR941-1, 4 more genes
    nsv5381223copy number variation2nstd102humanUncertain significance GRCh37 chr20: 60,831,241-62,664,346 , GRCh38.p12 chr20: 62,256,185-64,032,993 KCNQ2-AS1, HAR1B, 100 more genes
    nsv5321942copy number variation1nstd204human GRCh37.p13 chr20: 62,550,795-62,551,430 , GRCh38.p13 chr20: 63,919,442-63,920,077 DNAJC5, MIR941-1, 4 more genes
    nsv5321362copy number variation1nstd204human GRCh37.p13 chr20: 62,548,743-62,550,064 , GRCh38.p13 chr20: 63,917,390-63,918,711 DNAJC5, MIR941-1, 4 more genes
    nsv5293467copy number variation1nstd204human GRCh38.p13 chr20: 62,966,101-64,149,200 , GRCh37.p13 chr20: 61,597,453-62,780,553 , ZGPAT, 72 more genes
    nsv5286918copy number variation1nstd204human GRCh38.p13 chr20: 63,836,601-63,964,800 , GRCh37.p13 chr20: 62,467,954-62,596,153 DNAJC5, C20orf181, 14 more genes
    nsv5282963copy number variation1nstd204human GRCh38.p13 chr20: 63,863,001-64,088,600 , GRCh37.p13 chr20: 62,494,354-62,719,953 DNAJC5, RGS19, 22 more genes
    nsv5025831copy number variation1nstd200human GRCh38 chr20: 63,914,748-63,926,158 , GRCh37.p13 chr20: 62,546,101-62,557,511 DNAJC5, MIR941-4, 4 more genes
    nsv5022628copy number variation1nstd200human GRCh38 chr20: 63,914,388-63,918,609 , GRCh37.p13 chr20: 62,545,741-62,549,962 DNAJC5, MIR941-1, 4 more genes
    nsv4746914copy number variation1nstd199human GRCh37 chr20: 62,551,039-62,551,235 , GRCh38.p12 chr20: 63,919,686-63,919,882 DNAJC5, MIR941-1, 4 more genes
    nsv4729740copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,975,605-62,915,555 , GRCh38.p12 chr20: 63,344,253-64,284,202 STMN3, KCNQ2-AS1, 53 more genes
    nsv4681029copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr20: 61,977,556-62,562,941 , GRCh38.p12 chr20: 63,346,204-63,931,588 RNU1-134P, MIR941-5, 35 more genes
    nsv4676208copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,152,321-62,915,555 , GRCh38.p12 chr20: 62,555,114-64,284,202 GMEB2, LOC105372727, 94 more genes
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