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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
    nsv5025743copy number variation1nstd200human GRCh38 chr20: 55,396,562-55,729,773 , GRCh37.p13 chr20|NW_004504304.1: 34,494-283,551 , GRCh37.p13 chr20: 54,013,100-54,220,677 LINC01440, LOC107984001, 2 more genes
    nsv5013250copy number variation1nstd200human GRCh38 chr20: 55,424,967-55,429,149 , GRCh37.p13 chr20|NW_004504304.1: 62,899-67,081 , GRCh37.p13 chr20: 54,041,505-54,045,687 LINC01440, LINC01441
    nsv5013240copy number variation1nstd200human GRCh38 chr20: 55,147,720-55,522,471 , GRCh37.p13 chr20: 53,764,259-53,978,606 LINC01440, LINC01441
    nsv4865656copy number variation1nstd200human GRCh37 chr20: 54,013,100-54,304,829 , GRCh38.p12 chr20: 55,396,562-55,729,773 LOC105372676, LINC01441, 2 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
    nsv4292299copy number variation1nstd166human GRCh37.p13 chr20: 54,040,656-54,041,144 , GRCh38.p12 chr20: 55,424,118-55,424,606 LINC01441, LINC01440
    nsv4282482copy number variation1nstd166human GRCh37.p13 chr20: 54,042,608-54,043,094 , GRCh38.p12 chr20: 55,426,070-55,426,556 LINC01441, LINC01440
    nsv3970053copy number variation1nstd168human GRCh38 chr20: 55,352,187-55,442,371 , GRCh37.p13 chr20|NW_004504304.1: 1-80,303 , GRCh37.p13 chr20: 53,979,254-54,058,909 LINC01441, LINC01440
    nsv3922413copy number variation1nstd102humanUncertain significance NCBI36 chr20: 52,452,608-53,804,360 , GRCh37 chr20: 53,019,201-54,370,953 , GRCh38 chr20: 54,402,662-55,795,897 RPL12P4, LINC01441, 5 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
    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
    nsv3909941copy number variation1nstd102humanLikely benign NCBI36 chr20: 53,167,124-53,579,614 , GRCh37.p13 chr20|NW_004504304.1: 1-209,081 , GRCh37.p13 chr20: 53,733,717-54,146,207 , GRCh38.p12 chr20: 55,117,178-55,571,149 LINC01441, LINC01440
    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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