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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
    nsv7005544copy number variation1nstd229human GRCh38 chr20: 268,488-273,895 , GRCh37.p13 chr20: 249,129-254,536 C20orf96
    nsv6637884copy number variation1nstd102humanUncertain significance GRCh37 chr20: 79,455-347,319 , GRCh38.p12 chr20: 98,814-366,675 DEFB126, ZCCHC3, 9 more genes
    nsv6597092inversion1nstd223human GRCh38 chr20: 285,656-286,269 , GRCh37.p13 chr20: 266,297-266,910 C20orf96
    nsv6530962copy number variation1nstd223human GRCh38 chr20: 273,931-278,968 , GRCh37.p13 chr20: 254,572-259,609 C20orf96
    nsv6314010copy number variation1nstd102humanUncertain significance GRCh37 chr20: 242,496-742,740 , GRCh38.p12 chr20: 261,855-762,096 C20orf96, RBCK1, 13 more genes
    nsv6288174insertion1nstd214human GRCh38 chr20: 280,278-280,278 , GRCh37.p13 chr20: 260,919-260,919 C20orf96
    nsv6284490copy number variation1nstd214human GRCh38 chr20: 280,211-280,274 , GRCh37.p13 chr20: 260,852-260,915 C20orf96
    nsv6284407copy number variation1nstd214human GRCh38 chr20: 278,954-279,081 , GRCh37.p13 chr20: 259,595-259,722 C20orf96
    nsv6284107copy number variation1nstd214human GRCh38 chr20: 280,211-280,338 , GRCh37.p13 chr20: 260,852-260,979 C20orf96
    nsv6283527copy number variation1nstd214human GRCh38 chr20: 278,974-279,037 , GRCh37.p13 chr20: 259,615-259,678 C20orf96
    nsv6281762copy number variation1nstd214human GRCh38 chr20: 279,074-279,141 , GRCh37.p13 chr20: 259,715-259,782 C20orf96
    nsv6276427copy number variation1nstd214human GRCh38 chr20: 278,937-279,044 , GRCh37.p13 chr20: 259,578-259,685 C20orf96
    nsv6234453insertion1nstd214human GRCh38 chr20: 280,230-280,230 , GRCh37.p13 chr20: 260,871-260,871 C20orf96
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