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Items: 1 to 20 of 588

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148267copy number variation1nstd102humanPathogenic GRCh38 chr20: 87,153-23,635,465 , GRCh37.p13 chr20: 67,794-23,616,102 KRT18P3, RSPO4, 413 more genes
    nsv7098816copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 3,005,123-5,547,871 , GRCh38.p12 chr20: 3,024,477-5,567,225 ADRA1D, AVP, 70 more genes
    nsv7095892copy number variation1nstd102humanUncertain significance GRCh37 chr20: 3,515,880-3,521,002 , GRCh38.p12 chr20: 3,535,233-3,540,355 ATRN
    nsv7095879copy number variation2nstd102humanUncertain significance GRCh37 chr20: 1,959,939-6,760,201 , GRCh38.p12 chr20: 1,979,293-6,779,554 SLC23A2, TARDBPP1, 120 more genes
    nsv7095551copy number variation1nstd102humanPathogenic GRCh37 chr20: 3,063,276-3,903,941 , GRCh38.p12 chr20: 3,082,630-3,923,294 PANK2, MAVS, 31 more genes
    nsv7074742inversion1nstd229human GRCh38 chr20: 3,441,683-5,027,331 , GRCh37.p13 chr20: 3,422,330-5,007,977 MAVS, MIR103B2, 33 more genes
    nsv7074371inversion1nstd229human GRCh38 chr20: 2,515,505-5,510,656 , GRCh37.p13 chr20: 2,496,151-5,491,302 RPL19P1, DDRGK1, 87 more genes
    nsv7068018inversion1nstd229human GRCh38 chr20: 1,903,309-3,817,737 , GRCh37.p13 chr20: 1,883,955-3,798,384 PCED1A, UBOX5-AS1, 62 more genes
    nsv7062636inversion1nstd229human GRCh38 chr20: 3,532,145-3,535,941 , GRCh37.p13 chr20: 3,512,792-3,516,588 ATRN
    nsv7060166inversion1nstd229human GRCh38 chr20: 2,999,965-6,521,256 , GRCh37.p13 chr20: 2,980,611-6,501,903 FASTKD5, LOC101929098, 86 more genes
    nsv7059783inversion1nstd229human GRCh38 chr20: 3,527,319-3,536,106 , GRCh37.p13 chr20: 3,507,966-3,516,753 ATRN
    nsv7017395copy number variation1nstd229human GRCh38 chr20: 3,568,969-3,569,311 , GRCh37.p13 chr20: 3,549,616-3,549,958 ATRN
    nsv7015272copy number variation1nstd229human GRCh38 chr20: 3,519,388-3,799,972 , GRCh37.p13 chr20: 3,500,035-3,780,619 CDC25B, HSPA12B, 7 more genes
    nsv7014135copy number variation1nstd229human GRCh38 chr20: 3,572,501-3,585,400 , GRCh37.p13 chr20: 3,553,148-3,566,047 ATRN
    nsv7013432copy number variation1nstd229human GRCh38 chr20: 3,505,901-3,509,100 , GRCh37.p13 chr20: 3,486,548-3,489,747 ATRN
    nsv7012745copy number variation1nstd229human GRCh38 chr20: 3,505,953-3,511,867 , GRCh37.p13 chr20: 3,486,600-3,492,514 ATRN
    nsv7012531copy number variation1nstd229human GRCh38 chr20: 3,488,676-3,492,674 , GRCh37.p13 chr20: 3,469,323-3,473,321 ATRN, SF3A3P1
    nsv7012414copy number variation1nstd229human GRCh38 chr20: 3,498,052-3,503,307 , GRCh37.p13 chr20: 3,478,699-3,483,954 ATRN
    nsv7010836copy number variation1nstd229human GRCh38 chr20: 3,565,872-3,568,113 , GRCh37.p13 chr20: 3,546,519-3,548,760 ATRN
    nsv7007814copy number variation1nstd229human GRCh38 chr20: 3,492,001-3,505,500 , GRCh37.p13 chr20: 3,472,648-3,486,147 ATRN
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