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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112778copy number variation1nstd102humanPathogenic GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273 LINC01742, MTCO2P1, 253 more genes
    nsv5526430copy number variation1nstd206human GRCh38 chr20: 54,214,406-54,215,297 , GRCh37.p13 chr20: 52,830,945-52,831,836 PFDN4
    nsv5013206copy number variation1nstd200human GRCh38 chr20: 54,213,557-54,213,684 , GRCh37.p13 chr20: 52,830,096-52,830,223 PFDN4
    nsv4626691copy number variation1nstd183human GRCh37 chr20: 52,260,603-53,268,303 , GRCh38.p12 chr20: 53,644,064-54,651,764 CYP24A1, PFDN4, 7 more genes
    nsv4387806copy number variation1nstd173human GRCh37 chr20: 52,536,856-54,563,547 , GRCh38.p12 chr20: 53,920,317-55,988,491 LINC01441, LOC107984001, 13 more genes
    nsv4274927copy number variation1nstd166human GRCh37.p13 chr20: 52,824,999-52,825,107 , GRCh38.p12 chr20: 54,208,460-54,208,568 PFDN4
    nsv3920218copy number variation1nstd102humanPathogenic GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118 MIR3646, NPEPL1, 1310 more genes
    nsv3916972copy number variation1nstd102humanPathogenic GRCh38 chr20: 49,947,237-55,875,406 , NCBI36 chr20: 47,997,181-53,883,869 , GRCh37 chr20: 48,563,774-54,450,462 UBE2V1, KRT18P4, 87 more genes
    nsv3915005copy number variation1nstd102humanPathogenic NCBI36 chr20: 42,849,759-62,379,118 , GRCh37 chr20: 43,416,345-62,908,674 , GRCh38 chr20: 44,787,704-64,277,321 FTLP1, RNA5SP487, 472 more genes
    nsv3910818copy number variation1nstd102humanUncertain significance NCBI36 chr20: 25,616,026-62,435,964 , GRCh37.p13 chr20: 25,668,026-62,965,520 , GRCh38.p12 chr20: 25,687,390-64,334,167 RNA5SP481, LOC105372625, 855 more genes
    nsv3910223copy number variation1nstd102humanLikely pathogenic NCBI36 chr20: 51,286,111-62,385,999 , GRCh37 chr20: 51,852,704-62,915,555 , GRCh38 chr20: 53,236,165-64,284,202 ATP5F1E, BMP7, 253 more genes
    nsv3905072copy number variation1nstd102humanPathogenic GRCh37 chr20: 63,244-62,948,788 , GRCh38.p12 chr20: 82,603-64,317,435 LRRN4, SNRPB, 1313 more genes
    nsv3896520copy number variation1nstd102humanPathogenic GRCh37 chr20: 63,244-62,912,463 , GRCh38.p12 chr20: 82,603-64,281,110 COMMD7, RNU7-6P, 1311 more genes
    nsv3895314copy number variation2nstd102humanPathogenic GRCh37 chr20: 61,569-62,915,555 , GRCh38.p12 chr20: 80,928-64,284,202 PKIG, LINC01523, 1311 more genes
    nsv3894116copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 51,542,616-62,915,555 , GRCh38.p12 chr20: 52,926,077-64,284,202 ATP5F1E, BMP7, 254 more genes
    nsv3892750copy number variation1nstd102humanPathogenic GRCh37 chr20: 63,244-62,961,294 , GRCh38.p12 chr20: 82,603-64,329,941 TGIF2-RAB5IF, LOC105372609, 1314 more genes
    esv4010589copy number variation1estd233human GRCh37 chr20: 52,535,000-56,724,000 , GRCh38.p12 chr20: 53,918,461-58,148,944 , BMP7, 67 more genes
    nsv2102549short tandem repeat5nstd128human GRCh37 chr20: 52,836,765-52,836,788 , GRCh38.p12 chr20: 54,220,226-54,220,249 PFDN4
    nsv2102548short tandem repeat1nstd128human GRCh37 chr20: 52,836,139-52,836,154 , GRCh38.p12 chr20: 54,219,600-54,219,615 PFDN4
    nsv2102547short tandem repeat4nstd128human GRCh37 chr20: 52,834,716-52,834,731 , GRCh38.p12 chr20: 54,218,177-54,218,192 PFDN4
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