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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
    nsv5962128copy number variation1nstd209human GRCh38 chr20: 56,499,928-56,500,245 , GRCh37.p13 chr20: 55,074,984-55,075,301 GCNT7, RTF2
    nsv5881683copy number variation1nstd209human GRCh38 chr20: 56,525,687-56,536,614 , GRCh37.p13 chr20: 55,100,743-55,111,670 GCNT7, FAM209A, 1 more genes
    nsv5527111copy number variation1nstd206human GRCh38 chr20: 56,496,059-56,496,636 , GRCh37.p13 chr20: 55,071,115-55,071,692 , RTF2, 1 more genes
    nsv5517638copy number variation1nstd206human GRCh38 chr20: 56,521,189-56,521,356 , GRCh37.p13 chr20: 55,096,245-55,096,412 GCNT7
    nsv5350492translocation1nstd200human GRCh38 chr20: 56,522,227-56,522,227 , GRCh38 chr20: 56,536,337-56,536,337 , GRCh37.p13 chr20: 55,097,283-55,097,283 , GRCh37.p13 chr20: 55,111,393-55,111,393 GCNT7, FAM209B
    nsv5172825mobile element insertion1nstd203human GRCh38 chr20: 56,502,574-56,502,584 , GRCh37.p13 chr20: 55,077,630-55,077,640 GCNT7, RTF2
    nsv5025751copy number variation1nstd200human GRCh38 chr20: 56,510,773-56,538,566 , GRCh37.p13 chr20: 55,085,829-55,113,622 RTF2, FAM209A, 2 more genes
    nsv5013299copy number variation1nstd200human GRCh38 chr20: 56,523,317-56,531,119 , GRCh37.p13 chr20: 55,098,373-55,106,175 FAM209B, GCNT7, 1 more genes
    nsv5013298copy number variation1nstd200human GRCh38 chr20: 56,521,229-56,521,316 , GRCh37.p13 chr20: 55,096,285-55,096,372 GCNT7
    nsv5013297copy number variation1nstd200human GRCh38 chr20: 56,511,482-56,513,065 , GRCh37.p13 chr20: 55,086,538-55,088,121 RTF2, GCNT7
    nsv5013296copy number variation1nstd200human GRCh38 chr20: 56,491,771-56,492,638 , GRCh37.p13 chr20: 55,066,827-55,067,694 RTF2, GCNT7
    nsv4853985copy number variation1nstd200human GRCh37 chr20: 55,098,373-55,106,175 , GRCh38.p12 chr20: 56,523,317-56,531,119 FAM209B, GCNT7, 1 more genes
    nsv4853984copy number variation1nstd200human GRCh37 chr20: 55,086,538-55,088,121 , GRCh38.p12 chr20: 56,511,482-56,513,065 GCNT7, RTF2
    nsv4853983copy number variation1nstd200human GRCh37 chr20: 55,075,021-55,075,301 , GRCh38.p12 chr20: 56,499,965-56,500,245 GCNT7, RTF2
    nsv4680243copy number variation1nstd189human GRCh37.p13 chr20: 55,056,882-55,294,109 , GRCh38.p12 chr20: 56,481,826-56,719,053 , TFAP2C, 9 more genes
    nsv4621727copy number variation1nstd183human GRCh37 chr20: 55,070,289-55,070,966 , GRCh38.p12 chr20: 56,495,233-56,495,910 , RTF2, 1 more genes
    nsv4569998insertion1nstd166human GRCh37.p13 chr20: 55,070,156-55,070,156 , GRCh38.p12 chr20: 56,495,100-56,495,100 GCNT7, RTF2
    nsv4514314mobile element insertion1nstd166human GRCh37.p13 chr20: 55,077,630-55,077,630 , GRCh38.p12 chr20: 56,502,574-56,502,574 GCNT7, RTF2
    nsv4512211mobile element insertion1nstd166human GRCh37.p13 chr20: 55,073,849-55,073,849 , GRCh38.p12 chr20: 56,498,793-56,498,793 , RTF2, 1 more genes
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