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Items: 1 to 20 of 115

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147493insertion1nstd232human GRCh37.p13 chr20: 47,895,747-47,895,747 , GRCh38.p12 chr20: 49,279,210-49,279,210 SNORD12C, ZFAS1, 2 more genes
    nsv7075103inversion1nstd229human GRCh38 chr20: 48,844,229-55,780,453 , GRCh37.p13 chr20: 47,460,766-54,355,509 RPL12P4, LOC105372664, 113 more genes
    nsv7065344inversion1nstd229human GRCh38 chr20: 49,128,244-52,291,086 , GRCh37.p13 chr20: 47,744,781-50,907,625 PARD6B, LOC105372657, 77 more genes
    nsv7064075inversion1nstd229human GRCh38 chr20: 49,009,324-55,851,498 , GRCh37.p13 chr20: 47,625,861-54,426,554 DPM1, KCNG1, 115 more genes
    nsv7026019copy number variation1nstd229human GRCh38 chr20: 49,259,587-49,376,367 , GRCh37.p13 chr20: 47,876,124-47,992,904 SNORD12B, KCNB1, 5 more genes
    nsv7023332copy number variation1nstd229human GRCh38 chr20: 49,259,957-49,280,881 , GRCh37.p13 chr20: 47,876,494-47,897,418 ZFAS1, ZNFX1, 3 more genes
    nsv7020016copy number variation1nstd229human GRCh38 chr20: 49,254,626-49,283,829 , GRCh37.p13 chr20: 47,871,163-47,900,366 SNORD12B, SNORD12C, 3 more genes
    nsv6555071copy number variation1nstd223human GRCh38 chr20: 49,212,886-49,410,642 , GRCh37.p13 chr20: 47,829,423-48,027,179 KCNB1, DDX27, 7 more genes
    nsv6539092copy number variation1nstd223human GRCh38 chr20: 49,254,626-49,283,826 , GRCh37.p13 chr20: 47,871,163-47,900,363 SNORD12, ZFAS1, 3 more genes
    nsv6290315copy number variation1nstd102humanPathogenic GRCh37 chr20: 42,985,044-48,599,046 , GRCh38.p12 chr20: 44,356,404-49,982,509 PABPC1L, LOC107985401, 170 more genes
    nsv6134038copy number variation1nstd213human GRCh37 chr20: 46,610,000-48,330,001 , GRCh38.p12 chr20: 47,981,256-49,713,464 KCNB1, ZFAS1, 31 more genes
    nsv6133823copy number variation1nstd213human GRCh37 chr20: 47,890,000-48,840,001 , GRCh38.p12 chr20: 49,273,463-50,223,464 PTGIS, ZNFX1, 33 more genes
    nsv6112696copy number variation1nstd102humanUncertain significance GRCh38 chr20: 49,212,886-49,410,642 , GRCh37.p13 chr20: 47,829,423-48,027,179 KCNB1, DDX27, 7 more genes
    nsv5293775copy number variation1nstd204human GRCh38.p13 chr20: 49,278,301-49,289,700 , GRCh37.p13 chr20: 47,894,838-47,906,237 SNORD12C, SNORD12, 3 more genes
    nsv5025681copy number variation1nstd200human GRCh38 chr20: 49,254,626-49,283,829 , GRCh37.p13 chr20: 47,871,163-47,900,366 SNORD12C, SNORD12B, 3 more genes
    nsv4865618copy number variation1nstd200human GRCh37 chr20: 47,850,715-47,897,504 , GRCh38.p12 chr20: 49,234,178-49,280,967 ZNFX1, SNORD12, 4 more genes
    nsv4681865copy number variation1nstd102humanUncertain significance GRCh37 chr20: 47,538,407-48,099,037 , GRCh38.p12 chr20: 48,921,870-49,482,500 ARFGEF2, LOC105372649, 12 more genes
    nsv4632839copy number variation1nstd183human GRCh37 chr20: 47,892,453-47,895,183 , GRCh38.p12 chr20: 49,275,916-49,278,646 ZNFX1, SNORD12C, 2 more genes
    nsv4630531copy number variation1nstd183human GRCh37 chr20: 47,894,640-47,906,255 , GRCh38.p12 chr20: 49,278,103-49,289,718 ZFAS1, SNORD12C, 3 more genes
    nsv4621478copy number variation1nstd183human GRCh37 chr20: 47,752,123-47,988,180 , GRCh38.p12 chr20: 49,135,586-49,371,643 SNORD12, STAU1, 8 more genes
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