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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
    nsv5178576mobile element insertion1nstd203human GRCh38 chr20: 57,563,859-57,563,875 , GRCh37.p13 chr20: 56,138,915-56,138,931 PCK1
    nsv4678958copy number variation1nstd189human GRCh37.p13 chr20: 55,665,635-56,143,223 , GRCh38.p12 chr20: 57,090,579-57,568,167 BMP7, PCK1, 17 more genes
    nsv4676332copy number variation1nstd102humanPathogenic GRCh37 chr20: 55,743,522-62,032,989 , GRCh38.p12 chr20: 57,168,466-63,401,636 BMP7, MIR298, 153 more genes
    nsv4507915mobile element insertion1nstd166human GRCh37.p13 chr20: 56,138,915-56,138,915 , GRCh38.p12 chr20: 57,563,859-57,563,859 PCK1
    nsv4357849copy number variation1nstd102humanPathogenic GRCh37 chr20: 54,143,747-62,194,881 , GRCh38.p12 chr20: 55,568,689-63,563,528 RBM38, LAMA5, 192 more genes
    nsv4285332copy number variation1nstd166human GRCh37.p13 chr20: 56,132,845-56,135,620 , GRCh38.p12 chr20: 57,557,789-57,560,564 PCK1
    nsv4277958copy number variation1nstd166human GRCh37.p13 chr20: 56,125,980-56,947,246 , GRCh38.p12 chr20: 57,550,924-58,372,190 , LINC01742, 14 more genes
    nsv4275037copy number variation1nstd166human GRCh37.p13 chr20: 55,859,838-56,531,739 , GRCh38.p12 chr20: 57,284,782-57,956,683 , MTND1P9, 17 more genes
    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
    nsv3918295copy number variation1nstd102humanPathogenic GRCh38 chr20: 54,594,888-58,190,583 , NCBI36 chr20: 52,644,834-56,199,045 , GRCh37 chr20: 53,211,427-56,765,639 MTRNR2L3, LOC105372687, 59 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
    nsv3912982copy number variation1nstd102humanLikely pathogenic NCBI36 chr20: 53,639,062-58,949,658 , GRCh37 chr20: 54,220,678-59,516,263 , GRCh38 chr20: 55,630,597-60,941,207 ATP5F1E, BMP7, 103 more genes
    nsv3911673copy number variation1nstd102humanPathogenic GRCh37 chr20: 54,773,088-62,908,674 , NCBI36 chr20: 54,206,495-62,379,118 , GRCh38 chr20: 56,198,032-64,277,321 LOC105372709, NPBWR2, 226 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
    nsv3910216copy number variation1nstd102humanPathogenic GRCh37 chr20: 55,804,471-62,904,442 , NCBI36 chr20: 55,237,878-62,374,886 , GRCh38 chr20: 57,229,415-64,273,089 GID8, LOC105372708, 204 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
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