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Items: 1 to 20 of 219

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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
    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
    nsv7011095copy number variation1nstd229human GRCh38 chr20: 259,792-265,724 , GRCh37.p13 chr20: 240,433-246,365 DEFB132
    nsv7010453copy number variation1nstd229human GRCh38 chr20: 256,763-266,683 , GRCh37.p13 chr20: 237,404-247,324 DEFB132
    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
    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
    nsv5868207copy number variation1nstd209human GRCh38 chr20: 253,895-264,031 , GRCh37.p13 chr20: 234,536-244,672 DEFB132
    nsv5533226copy number variation1nstd206human GRCh38 chr20: 68,334-3,826,335 , GRCh37.p13 chr20: 60,002-3,806,982 , SNORD110, 125 more genes
    nsv5520553copy number variation1nstd206human GRCh38 chr20: 137,830-261,757 , GRCh37.p13 chr20: 118,471-242,398 DEFB126, DEFB127, 3 more genes
    nsv5518936copy number variation1nstd206human GRCh38 chr20: 254,167-270,335 , GRCh37.p13 chr20: 234,808-250,976 DEFB132, C20orf96
    nsv5381806copy number variation1nstd102humanPathogenic GRCh37 chr20: 67,778-974,841 , GRCh38.p12 chr20: 87,137-994,198 DEFB132, LOC101929937, 24 more genes
    nsv5324021copy number variation1nstd204human GRCh38.p13 chr20: 255,785-255,950 , GRCh37.p13 chr20: 236,426-236,591 DEFB132
    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
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