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Items: 1 to 20 of 214

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148186copy number variation1nstd102humanUncertain significance GRCh37 chr20: 52,773,668-62,965,020 , GRCh38.p12 chr20: 54,157,129-64,333,667 LOC105372717, CTCFL, 245 more genes
    nsv7148178copy number variation1nstd102humanPathogenic GRCh38 chr20: 62,632,017-63,794,804 , GRCh37.p13 chr20: 61,267,734-62,426,157 GID8, TCFL5, 60 more genes
    nsv7096264copy number variation2nstd102humanUncertain significance GRCh37 chr20: 60,831,241-62,680,869 , GRCh38.p12 chr20: 62,256,185-64,049,516 RPS21, MIR1-1HG, 102 more genes
    nsv7096082copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr20: 61,978,090-62,324,656 , GRCh38.p12 chr20: 63,346,738-63,693,303 SRMS, KCNQ2, 17 more genes
    nsv7095915copy number variation2nstd102humanPathogenic GRCh37 chr20: 62,075,992-62,324,656 , GRCh38.p12 chr20: 63,444,639-63,693,303 LOC105372725, PPDPF, 13 more genes
    nsv7065985inversion1nstd229human GRCh38 chr20: 63,509,212-64,282,670 , GRCh37.p13 chr20: 62,140,565-62,914,023 RNU1-134P, MIR6813, 46 more genes
    nsv7061289inversion1nstd229human GRCh38 chr20: 63,026,492-64,008,482 , GRCh37.p13 chr20: 61,657,844-62,639,835 TNFRSF6B, MIR941-5, 60 more genes
    nsv7059476inversion1nstd229human GRCh38 chr20: 63,024,183-64,005,567 , GRCh37.p13 chr20: 61,655,535-62,636,920 RTEL1-TNFRSF6B, LOC105372721, 60 more genes
    nsv7037078copy number variation1nstd229human GRCh38 chr20: 54,988,450-63,850,628 , GRCh37.p13 chr20: 53,604,989-62,481,981 , RPL39P, 209 more genes
    nsv7028474copy number variation1nstd229human GRCh38 chr20: 63,628,887-63,632,217 , GRCh37.p13 chr20: 62,260,240-62,263,570 MHENCR
    nsv6637836copy number variation1nstd102humanUncertain significance GRCh37 chr20: 60,621,074-62,915,555 , GRCh38.p12 chr20: 62,046,018-64,284,202 SLC17A9, MIR3195, 120 more genes
    nsv6598525inversion1nstd223human GRCh38 chr20: 63,626,801-63,956,899 , GRCh37.p13 chr20: 62,258,154-62,588,252 SLC2A4RG, ABHD16B, 26 more genes
    nsv6315308copy number variation1nstd102humanUncertain significance GRCh38 chr20: 61,800,345-63,644,611 , GRCh37.p13 chr20: 60,375,401-62,275,964 STMN3, RPS21, 86 more genes
    nsv6315031copy number variation1nstd102humanUncertain significance GRCh38 chr20: 62,941,782-63,658,260 , GRCh37.p13 chr20: 61,573,134-62,289,613 GMEB2, LOC105372724, 38 more genes
    nsv6314208copy number variation1nstd102humanPathogenic GRCh37 chr20: 56,835,739-62,915,555 , GRCh38.p12 chr20: 58,260,683-64,284,202 LOC105372698, LOC105372695, 176 more genes
    nsv6314138copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,797,521-62,318,983 , GRCh38.p12 chr20: 63,166,169-63,687,630 HELZ2, MIR124-3, 27 more genes
    nsv6314131copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,003,263-62,915,555 , GRCh38.p12 chr20: 62,428,207-64,284,202 HAR1A, PPDPF, 100 more genes
    nsv6314091copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,619,222-62,915,555 , GRCh38.p12 chr20: 62,987,870-64,284,202 TPD52L2, MIR941-5, 72 more genes
    nsv6311237copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,987,307-62,329,916 , GRCh38.p12 chr20: 63,355,955-63,698,563 PPDPF, LOC105372725, 19 more genes
    nsv6291738copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,775,756-62,915,555 , GRCh38.p12 chr20: 63,144,404-64,284,202 PTK6, C20orf204, 63 more genes
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