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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096021copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 33,044,890-33,049,935 , GRCh38.p12 chr20: 34,457,085-34,462,130 ITCH
    nsv7095891copy number variation1nstd102humanPathogenic GRCh37 chr20: 33,057,833-33,077,751 , GRCh38.p12 chr20: 34,470,028-34,489,946 FDX1P1, ITCH
    nsv7095890copy number variation1nstd102humanUncertain significance GRCh37 chr20: 32,868,840-33,033,286 , GRCh38.p12 chr20: 34,281,034-34,445,481 ITCH, CDC42P1, 1 more genes
    nsv7095554copy number variation1nstd102humanUncertain significance GRCh37 chr20: 33,059,229-33,059,340 , GRCh38.p12 chr20: 34,471,424-34,471,535 ITCH, FDX1P1
    nsv7093293copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 33,033,222-33,033,223 , GRCh38 chr20: 34,445,417-34,445,418 ITCH
    nsv7060544inversion1nstd229human GRCh38 chr20: 34,359,005-34,717,370 , GRCh37.p13 chr20: 32,946,811-33,305,174 FDX1P1, PIGU, 8 more genes
    nsv7036910copy number variation1nstd229human GRCh38 chr20: 34,450,801-34,477,700 , GRCh37.p13 chr20: 33,038,606-33,065,505 FDX1P1, ITCH, 1 more genes
    nsv7035822copy number variation1nstd229human GRCh38 chr20: 34,380,848-34,387,717 , GRCh37.p13 chr20: 32,968,654-32,975,523 ITCH
    nsv7035712copy number variation1nstd229human GRCh38 chr20: 34,373,376-34,379,632 , GRCh37.p13 chr20: 32,961,182-32,967,438 ITCH
    nsv7033675copy number variation1nstd229human GRCh38 chr20: 34,503,777-34,503,833 , GRCh37.p13 chr20: 33,091,582-33,091,638 ITCH
    nsv7033341copy number variation1nstd229human GRCh38 chr20: 34,374,793-34,392,772 , GRCh37.p13 chr20: 32,962,599-32,980,578 ITCH
    nsv7033205copy number variation1nstd229human GRCh38 chr20: 34,482,875-34,482,935 , GRCh37.p13 chr20: 33,070,680-33,070,740 ITCH
    nsv7031876copy number variation1nstd229human GRCh38 chr20: 34,449,172-34,481,180 , GRCh37.p13 chr20: 33,036,977-33,068,985 MIR644A, FDX1P1, 1 more genes
    nsv7027981copy number variation1nstd229human GRCh38 chr20: 34,424,726-34,429,166 , GRCh37.p13 chr20: 33,012,532-33,016,972 ITCH
    nsv7027751copy number variation1nstd229human GRCh38 chr20: 34,373,345-34,379,665 , GRCh37.p13 chr20: 32,961,151-32,967,471 ITCH
    nsv7026559copy number variation1nstd229human GRCh38 chr20: 34,415,289-34,416,262 , GRCh37.p13 chr20: 33,003,095-33,004,068 ITCH
    nsv7025529copy number variation1nstd229human GRCh38 chr20: 34,491,638-34,491,797 , GRCh37.p13 chr20: 33,079,443-33,079,602 ITCH
    nsv7022589copy number variation1nstd229human GRCh38 chr20: 34,425,981-34,433,676 , GRCh37.p13 chr20: 33,013,787-33,021,482 ITCH
    nsv7021198copy number variation1nstd229human GRCh38 chr20: 33,145,032-41,995,765 , GRCh37.p13 chr20: 31,732,838-40,624,405 PXMP4, RPL12P11, 199 more genes
    nsv7020769copy number variation1nstd229human GRCh38 chr20: 34,372,101-34,379,600 , GRCh37.p13 chr20: 32,959,907-32,967,406 ITCH
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