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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6874906copy number variation1nstd229human GRCh38 chr9: 111,555,501-111,653,300 , GRCh37.p13 chr9: 114,317,781-114,415,580 ZNF483, DNAJC25-GNG10, 4 more genes
    nsv6873360copy number variation1nstd229human GRCh38 chr9: 111,494,875-111,906,695 , GRCh37.p13 chr9: 114,257,155-114,668,975 ZNF483, GNG10, 8 more genes
    nsv6867664copy number variation1nstd229human GRCh38 chr9: 111,645,476-111,648,492 , GRCh37.p13 chr9: 114,407,756-114,410,772 DNAJC25, DNAJC25-GNG10
    nsv6863570copy number variation1nstd229human GRCh38 chr9: 111,631,744-111,639,858 , GRCh37.p13 chr9: 114,394,024-114,402,138 DNAJC25, LOC107987116, 1 more genes
    nsv6862842copy number variation1nstd229human GRCh38 chr9: 111,639,560-111,663,022 , GRCh37.p13 chr9: 114,401,840-114,425,302 GNG10, DNAJC25-GNG10, 1 more genes
    nsv6862402copy number variation1nstd229human GRCh38 chr9: 111,631,741-111,639,858 , GRCh37.p13 chr9: 114,394,021-114,402,138 DNAJC25, LOC107987116, 1 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6559632inversion1nstd223human GRCh38 chr9: 111,652,251-111,652,736 , GRCh37.p13 chr9: 114,414,531-114,415,016 DNAJC25-GNG10, DNAJC25
    nsv6449634copy number variation1nstd223human GRCh38 chr9: 111,629,001-111,642,100 , GRCh37.p13 chr9: 114,391,281-114,404,380 DNAJC25-GNG10, DNAJC25, 1 more genes
    nsv6315460copy number variation1nstd102humanUncertain significance GRCh37 chr9: 113,673,200-115,935,268 , GRCh38.p12 chr9: 110,910,920-113,172,988 MIR4668, LINC02977, 40 more genes
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
    nsv6314062copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 109,265,628-117,650,999 , GRCh38.p12 chr9: 106,503,347-114,888,719 ALAD, AMBP, 151 more genes
    nsv6313900copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 71,349,994-122,603,410 , GRCh38.p12 chr9: 68,735,078-119,841,132 ABCA1, ALAD, 793 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6137435copy number variation1nstd213human GRCh37 chr9: 114,290,000-114,910,001 , GRCh38.p12 chr9: 111,527,720-112,147,721 PTGR1, DNAJC25-GNG10, 13 more genes
    nsv6136726copy number variation1nstd213human GRCh37 chr9: 114,140,000-114,620,001 , GRCh38.p12 chr9: 111,377,720-111,857,721 ECPAS, LOC107987116, 9 more genes
    nsv6136639copy number variation1nstd213human GRCh37 chr9: 114,260,000-114,500,001 , GRCh38.p12 chr9: 111,497,720-111,737,721 GNG10, PTGR1, 6 more genes
    nsv6085063insertion1nstd212human GRCh38 chr9: 111,641,201-111,641,201 , GRCh37.p13 chr9: 114,403,481-114,403,481 DNAJC25, DNAJC25-GNG10
    nsv6019607copy number variation1nstd212human GRCh38 chr9: 111,641,913-111,641,974 , GRCh37.p13 chr9: 114,404,193-114,404,254 DNAJC25-GNG10, DNAJC25
    nsv6015509copy number variation1nstd212human GRCh38 chr9: 111,641,130-111,641,360 , GRCh37.p13 chr9: 114,403,410-114,403,640 DNAJC25-GNG10, DNAJC25
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