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Items: 1 to 20 of 178

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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
    nsv7077895inversion1nstd229human GRCh38 chr20: 265,739-1,834,868 , GRCh37.p13 chr20: 246,380-1,815,514 PSMF1, LOC105372498, 46 more genes
    nsv7069591inversion1nstd229human GRCh38 chr20: 105,288-375,237 , GRCh37.p13 chr20: 85,929-355,881 DEFB126, DEFB128, 9 more genes
    nsv7016287copy number variation1nstd229human GRCh38 chr20: 95,107-296,217 , GRCh37.p13 chr20: 75,748-276,858 DEFB129, ZCCHC3, 6 more genes
    nsv7015109copy number variation1nstd229human GRCh38 chr20: 212,701-479,100 , GRCh37.p13 chr20: 193,342-459,744 C20orf96, RBCK1, 10 more genes
    nsv7008951copy number variation1nstd229human GRCh38 chr20: 267,035-295,903 , GRCh37.p13 chr20: 247,676-276,544 C20orf96, ZCCHC3
    nsv7007834copy number variation1nstd229human GRCh38 chr20: 208,997-952,202 , GRCh37.p13 chr20: 189,638-932,845 TBC1D20, NRSN2-AS1, 19 more genes
    nsv6637884copy number variation1nstd102humanUncertain significance GRCh37 chr20: 79,455-347,319 , GRCh38.p12 chr20: 98,814-366,675 DEFB126, ZCCHC3, 9 more genes
    nsv6314010copy number variation1nstd102humanUncertain significance GRCh37 chr20: 242,496-742,740 , GRCh38.p12 chr20: 261,855-762,096 C20orf96, RBCK1, 13 more genes
    nsv6134047copy number variation1nstd213human GRCh37 chr20: 60,000-470,001 , GRCh38.p12 chr20: 79,361-489,357 RBCK1, DEFB126, 14 more genes
    nsv6133904copy number variation1nstd213human GRCh37 chr20: 1-1,970,001 , GRCh38.p12 chr20: 79,361-1,989,355 , CSNK2A1, 57 more genes
    nsv5533226copy number variation1nstd206human GRCh38 chr20: 68,334-3,826,335 , GRCh37.p13 chr20: 60,002-3,806,982 , SNORD110, 125 more genes
    nsv5381806copy number variation1nstd102humanPathogenic GRCh37 chr20: 67,778-974,841 , GRCh38.p12 chr20: 87,137-994,198 DEFB132, LOC101929937, 24 more genes
    nsv5193643mobile element insertion1nstd203human GRCh38 chr20: 297,000-297,004 , GRCh37.p13 chr20: 277,641-277,645 ZCCHC3
    nsv4729808copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 61,568-677,437 , GRCh38.p12 chr20: 80,927-696,793 CSNK2A1, SOX12, 18 more genes
    nsv4684288copy number variation1nstd102humanPathogenic GRCh37 chr20: 63,244-813,880 , GRCh38.p12 chr20: 82,603-833,237 DEFB129, C20orf96, 20 more genes
    nsv4680506copy number variation1nstd189human GRCh37.p13 chr20: 1-627,290 , GRCh38.p12 chr20: 79,361-646,646 , CSNK2A1, 17 more genes
    nsv4680158copy number variation1nstd189human GRCh37.p13 chr20: 176,577-517,161 , GRCh38.p12 chr20: 195,936-536,517 CSNK2A1, SOX12, 10 more genes
    nsv4676288copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,568-1,305,971 , GRCh38.p12 chr20: 80,927-1,325,327 TBC1D20, RAD21L1, 34 more genes
    nsv4676270copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,568-2,269,777 , GRCh38.p12 chr20: 80,927-2,289,131 LOC100289473, STK35, 60 more genes
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