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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6123581copy number variation1nstd186human GRCh37 chr20: 58,906,489-58,906,585 , GRCh38.p12 chr20: 60,331,431-60,331,527 LOC105372697
    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
    nsv5964958copy number variation1nstd209human GRCh38 chr20: 60,331,431-60,331,486 , GRCh37.p13 chr20: 58,906,489-58,906,544 LOC105372697
    nsv5957625copy number variation1nstd209human GRCh38 chr20: 60,331,439-60,331,494 , GRCh37.p13 chr20: 58,906,497-58,906,552 LOC105372697
    nsv5669649insertion1nstd207human GRCh38 chr20: 60,331,431-60,331,431 , GRCh37.p13 chr20: 58,906,489-58,906,489 LOC105372697
    nsv5520877copy number variation1nstd206human GRCh38 chr20: 60,331,431-60,331,527 , GRCh37.p13 chr20: 58,906,489-58,906,585 LOC105372697
    nsv5180414mobile element insertion1nstd203human GRCh38 chr20: 60,331,965-60,331,979 , GRCh37.p13 chr20: 58,907,023-58,907,037 LOC105372697
    nsv5025771copy number variation1nstd200human GRCh38 chr20: 60,155,509-60,990,304 , GRCh37.p13 chr20: 58,730,565-59,565,360 MIR646, MIR4533, 8 more genes
    nsv5013404copy number variation1nstd200human GRCh38 chr20: 60,330,001-60,333,432 , GRCh37.p13 chr20: 58,905,059-58,908,490 LOC105372697
    nsv4865679copy number variation1nstd200human GRCh37 chr20: 58,730,565-59,565,360 , GRCh38.p12 chr20: 60,155,509-60,990,304 LOC105372698, MIR4533, 8 more genes
    nsv4755403insertion1nstd199human GRCh37 chr20: 58,906,514-58,906,514 , GRCh38.p12 chr20: 60,331,456-60,331,456 LOC105372697
    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
    nsv4676181copy number variation1nstd102humanPathogenic GRCh37 chr20: 56,788,101-62,762,405 , GRCh38.p12 chr20: 58,213,045-64,131,052 LOC105372697, MIR647, 174 more genes
    nsv4561890mobile element insertion1nstd166human GRCh37.p13 chr20: 58,907,023-58,907,023 , GRCh38.p12 chr20: 60,331,965-60,331,965 LOC105372697
    nsv4379691copy number variation1nstd173human GRCh37 chr20: 58,742,917-58,930,497 , GRCh38.p12 chr20: 60,167,859-60,355,439 LOC105372698, MIR646, 2 more genes
    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
    nsv4283753copy number variation1nstd166human GRCh37.p13 chr20: 58,570,994-59,099,389 , GRCh38.p12 chr20: 59,995,939-60,524,331 , LOC729296, 9 more genes
    nsv3967173insertion1nstd168human GRCh38 chr20: 60,313,252-60,337,424 , GRCh37.p13 chr20: 58,888,310-58,912,482 LOC105372697, MIR646HG
    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
    nsv3916789copy number variation1nstd102humanPathogenic GRCh37 chr20: 57,617,021-62,908,674 , GRCh38 chr20: 59,041,966-64,277,321 , NCBI36 chr20: 57,050,416-62,379,118 RNU7-141P, UCKL1, 153 more genes
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