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Items: 1 to 20 of 193

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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
    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
    nsv7096087copy number variation1nstd102humanUncertain significance GRCh37 chr20: 62,559,699-62,680,869 , GRCh38.p12 chr20: 63,928,346-64,049,516 ZNF512B, MIR647, 9 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
    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
    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
    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
    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
    nsv6290337copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 61,038,552-62,907,579 , GRCh38.p12 chr20: 62,463,496-64,276,226 CHRNA4, COL9A3, 99 more genes
    nsv6290297copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 61,041,481-62,680,992 , GRCh38.p12 chr20: 62,466,425-64,049,639 CHRNA4, COL9A3, 91 more genes
    nsv6290296copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 61,273,854-62,907,579 , GRCh38.p12 chr20: 62,642,502-64,276,226 CHRNA4, COL9A3, 90 more genes
    nsv6134181copy number variation1nstd213human GRCh37 chr20: 61,440,000-62,920,001 , GRCh38.p12 chr20: 62,808,648-64,288,648 CHRNA4, KCNQ2, 82 more genes
    nsv6134180copy number variation1nstd213human GRCh37 chr20: 61,370,000-62,910,001 , GRCh38.p12 chr20: 62,738,648-64,278,648 , KCNQ2, 88 more genes
    nsv6134086copy number variation1nstd213human GRCh37 chr20: 61,270,000-62,920,001 , GRCh38.p12 chr20: 62,638,648-64,288,648 , EEF1A2, 91 more genes
    nsv6134048copy number variation1nstd213human GRCh37 chr20: 61,440,000-62,930,001 , GRCh38.p12 chr20: 62,808,648-64,298,648 CHRNA4, KCNQ2, 84 more genes
    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
    nsv6104427insertion1nstd212human GRCh38 chr20: 64,034,860-64,034,860 , GRCh37.p13 chr20: 62,666,213-62,666,213 C20orf204
    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
    nsv5297586copy number variation1nstd204human GRCh38.p13 chr20: 64,032,101-64,038,800 , GRCh37.p13 chr20: 62,663,454-62,670,153 C20orf204, PRPF6
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