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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5917134copy number variation1nstd209human GRCh38 chr8: 144,995,822-145,013,060 , GRCh37.p13 chr8: 146,221,208-146,238,446 ZNF252P, TMED10P1, 1 more genes
    nsv5866686copy number variation2nstd209human GRCh38 chr8: 144,998,944-145,002,843 , GRCh37.p13 chr8: 146,224,330-146,228,229 ZNF252P, TMED10P1, 1 more genes
    nsv5857317copy number variation2nstd209human GRCh38 chr8: 144,999,744-145,010,645 , GRCh37.p13 chr8: 146,225,130-146,236,031 ZNF252P-AS1, ZNF252P
    nsv5851532copy number variation2nstd209human GRCh38 chr8: 144,995,376-145,001,493 , GRCh37.p13 chr8: 146,220,762-146,226,879 ZNF252P, TMED10P1, 1 more genes
    nsv5848849copy number variation2nstd209human GRCh38 chr8: 144,997,626-145,001,443 , GRCh37.p13 chr8: 146,223,012-146,226,829 ZNF252P, ZNF252P-AS1, 1 more genes
    nsv5481227copy number variation1nstd206human GRCh38 chr8: 144,989,925-145,078,500 , GRCh37.p13 chr8: 146,215,311-146,303,886 TMED10P1, LOC100419763, 3 more genes
    nsv5480596copy number variation1nstd206human GRCh38 chr8: 144,997,650-145,009,464 , GRCh37.p13 chr8: 146,223,036-146,234,850 TMED10P1, ZNF252P, 1 more genes
    nsv5479229copy number variation1nstd206human GRCh38 chr8: 144,946,222-145,078,500 , GRCh37.p13 chr8: 146,171,608-146,303,886 ZNF16, C8orf33, 4 more genes
    nsv5315360copy number variation1nstd204human GRCh37.p13 chr8: 146,221,208-146,238,449 , GRCh38.p13 chr8: 144,995,822-145,013,063 ZNF252P, TMED10P1, 1 more genes
    nsv5257041copy number variation1nstd204human GRCh38.p13 chr8: 144,995,801-145,013,000 , GRCh37.p13 chr8: 146,221,187-146,238,386 ZNF252P, TMED10P1, 1 more genes
    nsv5247168copy number variation1nstd204human GRCh38.p13 chr8: 144,959,201-145,138,636 , GRCh37.p13 chr8: 146,184,587-146,304,022 ZNF252P, LOC100419763, 3 more genes
    nsv5246824copy number variation1nstd204human GRCh38.p13 chr8: 144,996,826-145,009,795 , GRCh37.p13 chr8: 146,222,212-146,235,181 TMED10P1, ZNF252P-AS1, 1 more genes
    nsv4969193copy number variation1nstd200human GRCh38 chr8: 144,997,848-145,072,507 , GRCh37.p13 chr8: 146,223,234-146,297,893 ZNF252P, LOC100419763, 3 more genes
    nsv4969189copy number variation1nstd200human GRCh38 chr8: 144,932,888-145,052,839 , GRCh37.p13 chr8: 146,158,274-146,278,225 ZNF252P-AS1, ZNF16, 4 more genes
    nsv4962769copy number variation1nstd200human GRCh38 chr8: 144,995,825-145,013,061 , GRCh37.p13 chr8: 146,221,211-146,238,447 TMED10P1, ZNF252P-AS1, 1 more genes
    nsv4822918copy number variation1nstd200human GRCh37 chr8: 146,223,036-146,234,850 , GRCh38.p12 chr8: 144,997,650-145,009,464 TMED10P1, ZNF252P, 1 more genes
    nsv4769373copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,033,244-146,297,937 , GRCh38.p12 chr8: 143,959,076-145,072,551 ZFTRAF1, PLEC, 68 more genes
    nsv4729603copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 144,262,042-146,295,771 , GRCh38.p12 chr8: 143,180,625-145,070,385 CYC1, EEF1D, 112 more genes
    nsv4675664copy number variation1nstd102humanPathogenic GRCh37 chr8: 128,877,995-146,295,771 , GRCh38.p12 chr8: 127,865,749-145,070,385 LOC105375789, LINC02990, 270 more genes
    nsv4675273copy number variation1nstd102humanPathogenic GRCh37 chr8: 121,042,467-146,295,771 , GRCh38.p12 chr8: 120,030,228-145,070,385 TOP1MT, SLA, 379 more genes
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