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Items: 1 to 20 of 177

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137705copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,419,493-40,774,118 , GRCh38.p12 chr9: 61,281,967-67,217,006 , GRCh38.p12 chr9: 36,419,496-39,445,729 ZNF658B, LOC105379814, 208 more genes
    nsv6137704copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,426,622-38,787,479 , GRCh38.p12 chr9: 36,426,625-38,787,482 MELK, SLC25A51, 55 more genes
    nsv6137702copy number variation1nstd102humanPathogenic GRCh37 chr9: 35,059,633-37,660,586 , GRCh38.p12 chr9: 35,059,636-37,660,589 ARHGEF39, LOC105376026, 84 more genes
    nsv6137700copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,088,563-39,092,820 , GRCh38.p12 chr9: 36,088,566-39,092,823 SNX18P3, VN1R48P, 69 more genes
    nsv5972210inversion1nstd209human GRCh38 chr9: 36,238,245-37,822,315 , GRCh37.p13 chr9: 36,238,242-37,822,312 PAX5, GRHPR, 35 more genes
    nsv5909428copy number variation1nstd209human GRCh38 chr9: 37,426,266-37,426,335 , GRCh37.p13 chr9: 37,426,263-37,426,332 GRHPR
    nsv5674291delins1nstd102humanPathogenic GRCh37 chr9: 37,426,594-37,426,597 , GRCh38 chr9: 37,426,597-37,426,600 GRHPR
    nsv5674173copy number variation1nstd102humanPathogenic GRCh37 chr9: 37,425,909-37,426,661 , GRCh38.p12 chr9: 37,425,912-37,426,664 GRHPR
    nsv5483580copy number variation1nstd206human GRCh38 chr9: 37,426,268-37,426,336 , GRCh37.p13 chr9: 37,426,265-37,426,333 GRHPR
    nsv5480716copy number variation1nstd206human GRCh38 chr9: 37,423,745-37,424,780 , GRCh37.p13 chr9: 37,423,742-37,424,777 GRHPR
    nsv5331601translocation1nstd200human GRCh37 chr9: 37,423,020-37,423,020 , GRCh37 chr4: 131,102,902-131,102,902 , GRCh38.p12 chr4: 130,181,747-130,181,747 , GRCh38.p12 chr9: 37,423,023-37,423,023 GRHPR
    nsv4766654inversion1nstd199human GRCh37 chr9: 201,453-68,434,063 , GRCh38.p12 chr9: 201,453-67,920,552 , ACO1, 876 more genes
    nsv4755256inversion1nstd199human GRCh37 chr9: 200,777-70,835,468 , GRCh38.p12 chr9: 200,777-67,920,552 , ACO1, 876 more genes
    nsv4729230copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 32,192,406-38,311,776 , GRCh38.p12 chr9: 32,192,408-38,311,779 ACO1, ANXA2P2, 210 more genes
    nsv4682597copy number variation1nstd102humanPathogenic GRCh37 chr9: 37,429,719-37,430,653 , GRCh38.p12 chr9: 37,429,722-37,430,656 GRHPR
    nsv4675565copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-70,984,588 , GRCh38.p12 chr9: 203,861-68,369,672 LOC100132004, LOC105375993, 853 more genes
    nsv4675481copy number variation1nstd102humanUncertain significance GRCh37 chr9: 36,539,229-38,787,480 , GRCh38.p12 chr9: 36,539,232-38,787,483 LOC105376042, CYP4F33P, 54 more genes
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4457200copy number variation2nstd102humanPathogenic GRCh37 chr9: 203,861-67,986,965 , GRCh38.p12 chr9: 203,861-67,919,519 ACO1, RNU6-1073P, 846 more genes
    nsv4456028copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-38,472,979 , GRCh38.p12 chr9: 203,861-38,472,982 SNORA30B, LOC100419692, 559 more genes
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