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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148267copy number variation1nstd102humanPathogenic GRCh38 chr20: 87,153-23,635,465 , GRCh37.p13 chr20: 67,794-23,616,102 KRT18P3, RSPO4, 413 more genes
    nsv7098816copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 3,005,123-5,547,871 , GRCh38.p12 chr20: 3,024,477-5,567,225 ADRA1D, AVP, 70 more genes
    nsv7096258copy number variation1nstd102humanPathogenic GRCh37 chr20: 3,888,553-3,888,945 , GRCh38.p12 chr20: 3,907,906-3,908,298 PANK2
    nsv7096077copy number variation1nstd102humanPathogenic GRCh37 chr20: 3,891,204-3,893,301 , GRCh38.p12 chr20: 3,910,557-3,912,654 PANK2
    nsv7095879copy number variation2nstd102humanUncertain significance GRCh37 chr20: 1,959,939-6,760,201 , GRCh38.p12 chr20: 1,979,293-6,779,554 SLC23A2, TARDBPP1, 120 more genes
    nsv7095560copy number variation1nstd102humanUncertain significance GRCh37 chr20: 3,869,748-3,893,301 , GRCh38.p12 chr20: 3,889,101-3,912,654 PANK2-AS1, PANK2
    nsv7095559copy number variation1nstd102humanPathogenic GRCh37 chr20: 3,869,748-3,891,497 , GRCh38.p12 chr20: 3,889,101-3,910,850 PANK2-AS1, PANK2
    nsv7095551copy number variation1nstd102humanPathogenic GRCh37 chr20: 3,063,276-3,903,941 , GRCh38.p12 chr20: 3,082,630-3,923,294 PANK2, MAVS, 31 more genes
    nsv7074742inversion1nstd229human GRCh38 chr20: 3,441,683-5,027,331 , GRCh37.p13 chr20: 3,422,330-5,007,977 MAVS, MIR103B2, 33 more genes
    nsv7074371inversion1nstd229human GRCh38 chr20: 2,515,505-5,510,656 , GRCh37.p13 chr20: 2,496,151-5,491,302 RPL19P1, DDRGK1, 87 more genes
    nsv7063954inversion1nstd229human GRCh38 chr20: 3,693,712-5,966,241 , GRCh37.p13 chr20: 3,674,359-5,946,887 GPCPD1, PANK2, 52 more genes
    nsv7060166inversion1nstd229human GRCh38 chr20: 2,999,965-6,521,256 , GRCh37.p13 chr20: 2,980,611-6,501,903 FASTKD5, LOC101929098, 86 more genes
    nsv7017314copy number variation1nstd229human GRCh38 chr20: 3,914,067-3,914,889 , GRCh37.p13 chr20: 3,894,714-3,895,536 PANK2
    nsv7015906copy number variation1nstd229human GRCh38 chr20: 3,898,101-3,905,600 , GRCh37.p13 chr20: 3,878,748-3,886,247 PANK2
    nsv7015155copy number variation1nstd229human GRCh38 chr20: 3,908,168-3,908,616 , GRCh37.p13 chr20: 3,888,815-3,889,263 PANK2
    nsv7011346copy number variation1nstd229human GRCh38 chr20: 3,859,068-3,914,068 , GRCh37.p13 chr20: 3,839,715-3,894,715 MAVS, PANK2, 1 more genes
    nsv7011090copy number variation1nstd229human GRCh38 chr20: 3,898,201-3,906,200 , GRCh37.p13 chr20: 3,878,848-3,886,847 PANK2
    nsv7009536copy number variation1nstd229human GRCh38 chr20: 3,860,350-3,915,364 , GRCh37.p13 chr20: 3,840,997-3,896,011 PANK2-AS1, PANK2, 1 more genes
    nsv7007840copy number variation1nstd229human GRCh38 chr20: 3,864,283-4,073,646 , GRCh37.p13 chr20: 3,844,930-4,054,293 RPL21P2, MAVS, 6 more genes
    nsv7007813copy number variation1nstd229human GRCh38 chr20: 3,543,154-3,905,714 , GRCh37.p13 chr20: 3,523,801-3,886,361 LINC01730, HSPA12B, 12 more genes
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