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Items: 1 to 20 of 175

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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
    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
    nsv7028864copy number variation1nstd229human GRCh38 chr20: 63,770,901-63,920,600 , GRCh37.p13 chr20: 62,402,254-62,551,953 DNAJC5, C20orf181, 11 more genes
    nsv7025635copy number variation1nstd229human GRCh38 chr20: 63,862,501-63,878,000 , GRCh37.p13 chr20: 62,493,854-62,509,353 LOC112268269, ABHD16B, 1 more genes
    nsv7024078copy number variation1nstd229human GRCh38 chr20: 63,862,721-63,867,235 , GRCh37.p13 chr20: 62,494,074-62,498,588 ABHD16B, TPD52L2, 1 more genes
    nsv7023427copy number variation1nstd229human GRCh38 chr20: 63,849,356-63,872,736 , GRCh37.p13 chr20: 62,480,709-62,504,089 LOC112268269, ABHD16B, 1 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
    nsv6598525inversion1nstd223human GRCh38 chr20: 63,626,801-63,956,899 , GRCh37.p13 chr20: 62,258,154-62,588,252 SLC2A4RG, ABHD16B, 26 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
    nsv6290321copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 61,826,780-62,660,844 , GRCh38.p12 chr20: 63,195,428-64,029,491 CHRNA4, EEF1A2, 51 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
    nsv6213017copy number variation1nstd214human GRCh38 chr20: 63,861,059-63,861,108 , GRCh37.p13 chr20: 62,492,412-62,492,461 ABHD16B, LOC112268269
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