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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
    nsv7138721copy number variation1nstd232human GRCh37.p13 chr20: 2,999,599-2,999,771 , GRCh38.p12 chr20: 3,018,953-3,019,125 PTPRA
    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
    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
    nsv7077358inversion1nstd229human GRCh38 chr20: 2,912,452-2,916,539 , GRCh37.p13 chr20: 2,893,098-2,897,185 PTPRA
    nsv7074371inversion1nstd229human GRCh38 chr20: 2,515,505-5,510,656 , GRCh37.p13 chr20: 2,496,151-5,491,302 RPL19P1, DDRGK1, 87 more genes
    nsv7068018inversion1nstd229human GRCh38 chr20: 1,903,309-3,817,737 , GRCh37.p13 chr20: 1,883,955-3,798,384 PCED1A, UBOX5-AS1, 62 more genes
    nsv7066680inversion1nstd229human GRCh38 chr20: 2,931,671-2,932,249 , GRCh37.p13 chr20: 2,912,317-2,912,895 PTPRA
    nsv7061358inversion1nstd229human GRCh38 chr20: 3,008,354-3,064,839 , GRCh37.p13 chr20: 2,989,000-3,045,485 PTPRA, MRPS26, 1 more genes
    nsv7060985inversion1nstd229human GRCh38 chr20: 2,809,464-3,136,537 , GRCh37.p13 chr20: 2,790,110-3,117,183 GNRH2, LOC101929098, 11 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
    nsv7060029inversion1nstd229human GRCh38 chr20: 2,839,465-3,184,791 , GRCh37.p13 chr20: 2,820,111-3,165,437 PCED1A, UBOX5-AS1, 12 more genes
    nsv7017845copy number variation1nstd229human GRCh38 chr20: 2,924,289-2,925,567 , GRCh37.p13 chr20: 2,904,935-2,906,213 PTPRA
    nsv7017153copy number variation1nstd229human GRCh38 chr20: 2,948,549-2,953,766 , GRCh37.p13 chr20: 2,929,195-2,934,412 PTPRA
    nsv7016507copy number variation1nstd229human GRCh38 chr20: 2,895,857-3,100,606 , GRCh37.p13 chr20: 2,876,503-3,081,252 RN7SL555P, AVP, 5 more genes
    nsv7016362copy number variation1nstd229human GRCh38 chr20: 2,989,347-2,991,279 , GRCh37.p13 chr20: 2,969,993-2,971,925 PTPRA
    nsv7016131copy number variation1nstd229human GRCh38 chr20: 2,927,042-2,928,359 , GRCh37.p13 chr20: 2,907,688-2,909,005 PTPRA
    nsv7015497copy number variation1nstd229human GRCh38 chr20: 3,032,550-3,033,658 , GRCh37.p13 chr20: 3,013,196-3,014,304 PTPRA
    nsv7014149copy number variation1nstd229human GRCh38 chr20: 3,029,075-3,029,197 , GRCh37.p13 chr20: 3,009,721-3,009,843 PTPRA
    nsv7013305copy number variation1nstd229human GRCh38 chr20: 2,900,056-2,909,453 , GRCh37.p13 chr20: 2,880,702-2,890,099 PTPRA
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