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Items: 1 to 20 of 130

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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
    nsv7095546copy number variation1nstd102humanPathogenic GRCh37 chr20: 17,587,682-18,168,103 , GRCh38.p12 chr20: 17,607,037-18,187,459 SNX5, PET117, 14 more genes
    nsv7073551inversion1nstd229human GRCh38 chr20: 10,362,744-19,023,342 , GRCh37.p13 chr20: 10,343,392-19,003,986 SLX4IP, RPL15P1, 122 more genes
    nsv7070199inversion1nstd229human GRCh38 chr20: 13,206,278-18,470,226 , GRCh37.p13 chr20: 13,186,925-18,450,870 LOC105372545, MACROD2, 73 more genes
    nsv7068244inversion1nstd229human GRCh38 chr20: 17,080,202-18,490,897 , GRCh37.p13 chr20: 17,060,847-18,471,541 DSTN, RNU2-56P, 42 more genes
    nsv7065399inversion1nstd229human GRCh38 chr20: 13,871,578-20,212,622 , GRCh37.p13 chr20: 13,852,224-20,193,266 SLC24A3, LOC107985418, 92 more genes
    nsv7036889copy number variation1nstd229human GRCh38 chr20: 18,133,210-18,142,492 , GRCh37.p13 chr20: 18,113,854-18,123,136 KAT14, PET117
    nsv7029165copy number variation1nstd229human GRCh38 chr20: 18,139,649-18,139,678 , GRCh37.p13 chr20: 18,120,293-18,120,322 PET117
    nsv7026289copy number variation1nstd229human GRCh38 chr20: 18,037,101-18,141,100 , GRCh37.p13 chr20: 18,017,745-18,121,744 RPL15P1, RNU7-137P, 3 more genes
    nsv7025823copy number variation1nstd229human GRCh38 chr20: 17,957,048-18,307,098 , GRCh37.p13 chr20: 17,937,692-18,287,742 RNU2-56P, SNORD17, 13 more genes
    nsv7021771copy number variation1nstd229human GRCh38 chr20: 18,143,494-18,154,324 , GRCh37.p13 chr20: 18,124,138-18,134,968 KAT14, PET117
    nsv6599358inversion1nstd223human GRCh38 chr20: 10,362,749-19,023,339 , GRCh37.p13 chr20: 10,343,397-19,003,983 JAG1, BFSP1, 122 more genes
    nsv6290339copy number variation1nstd102humanUncertain significance GRCh37 chr20: 11,702,911-19,179,706 , GRCh38.p12 chr20: 11,722,263-19,199,062 LOC105372530, MACROD2-AS1, 105 more genes
    nsv6134271copy number variation1nstd213human GRCh37 chr20: 15,280,000-18,930,001 , GRCh38.p12 chr20: 15,299,354-18,949,357 PTMAP3, SEC23B, 66 more genes
    nsv6134268copy number variation1nstd213human GRCh37 chr20: 13,380,000-22,450,001 , GRCh38.p12 chr20: 13,399,353-22,469,363 BFSP1, INSM1, 134 more genes
    nsv6133796copy number variation1nstd213human GRCh37 chr20: 18,100,000-18,370,001 , GRCh38.p12 chr20: 18,119,356-18,389,357 ZNF133, DZANK1, 11 more genes
    nsv5428540mobile element insertion1nstd206human GRCh38 chr20: 18,135,861-18,135,887 , GRCh37.p13 chr20: 18,116,505-18,116,531 PET117
    nsv5025180copy number variation1nstd200human GRCh38 chr20: 18,129,594-18,147,866 , GRCh37.p13 chr20: 18,110,238-18,128,510 PET117, KAT14
    nsv4676419copy number variation1nstd102humanPathogenic GRCh37 chr20: 8,571,696-22,088,650 , GRCh38.p12 chr20: 8,591,049-22,108,012 PGAM3P, EEF1A1P34, 182 more genes
    nsv4382417copy number variation1nstd173human GRCh37 chr20: 18,123,940-18,199,405 , GRCh38.p12 chr20: 18,143,296-18,218,761 KAT14, GGCTP2, 1 more genes
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