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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5522118copy number variation1nstd206human GRCh38 chr20: 46,492,104-46,492,203 , GRCh37.p13 chr20: 45,120,743-45,120,842 ZNF334, ZNF840P
    nsv5514524copy number variation1nstd206human GRCh38 chr20: 46,491,659-46,492,317 , GRCh37.p13 chr20: 45,120,298-45,120,956 ZNF334, ZNF840P
    nsv5326425copy number variation1nstd204human GRCh37.p13 chr20: 45,120,271-45,120,820 , GRCh38.p13 chr20: 46,491,632-46,492,181 ZNF840P, ZNF334
    nsv5025653copy number variation1nstd200human GRCh38 chr20: 46,372,673-46,616,535 , GRCh37.p13 chr20: 45,001,312-45,245,174 ZNF334, ELMO2, 6 more genes
    nsv5022342copy number variation1nstd200human GRCh38 chr20: 32,576,247-46,538,786 , GRCh37.p13 chr20: 31,164,049-45,167,425 , NECAB3, 350 more genes
    nsv4868593copy number variation1nstd200human GRCh37 chr20: 31,164,049-45,167,425 , GRCh38.p12 chr20: 32,576,247-46,538,786 , MMP24-AS1-EDEM2, 350 more genes
    nsv4865602copy number variation1nstd200human GRCh37 chr20: 45,001,312-45,245,174 , GRCh38.p12 chr20: 46,372,673-46,616,535 MKRN7P, ZNF334, 6 more genes
    nsv4853691copy number variation1nstd200human GRCh37 chr20: 45,120,251-45,120,926 , GRCh38.p12 chr20: 46,491,612-46,492,287 ZNF840P, ZNF334
    nsv4674805copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 34,980,430-46,806,549 , GRCh38.p12 chr20: 36,352,027-48,177,806 ADA, BPI, 266 more genes
    nsv4457624copy number variation1nstd102humanUncertain significance GRCh37 chr20: 45,002,981-45,243,034 , GRCh38.p12 chr20: 46,374,342-46,614,395 ZNF334, OCSTAMP, 6 more genes
    nsv4287513copy number variation1nstd166human GRCh37.p13 chr20: 45,120,256-45,120,487 , GRCh38.p12 chr20: 46,491,617-46,491,848 ZNF334, ZNF840P
    nsv4281162copy number variation1nstd166human GRCh37.p13 chr20: 45,120,337-45,120,966 , GRCh38.p12 chr20: 46,491,698-46,492,327 ZNF334, ZNF840P
    nsv4275139copy number variation1nstd166human GRCh37.p13 chr20: 45,001,312-45,245,065 , GRCh38.p12 chr20: 46,372,673-46,616,426 MKRN7P, ZNF334, 6 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
    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
    nsv3912723copy number variation1nstd102humanPathogenic NCBI36 chr20: 30,288,202-45,731,170 , GRCh37.p13 chr20: 30,824,541-46,297,763 , GRCh38.p12 chr20: 32,236,738-47,669,019 LOC107985448, LOC105372613, 370 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
    nsv3910049copy number variation1nstd102humanPathogenic NCBI36 chr20: 33,289,165-45,693,969 , GRCh37 chr20: 33,825,749-46,260,562 , GRCh38 chr20: 35,237,946-47,631,818 NDUFB4P10, EIF4EBP2P1, 291 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
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