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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
    nsv5925815copy number variation1nstd209human GRCh38 chr9: 37,502,510-37,515,062 , GRCh37.p13 chr9: 37,502,507-37,515,059 POLR1E, FBXO10
    nsv5866080copy number variation1nstd209human GRCh38 chr9: 37,484,139-37,489,383 , GRCh37.p13 chr9: 37,484,136-37,489,380 POLR1E, RPL21P83
    nsv5862237copy number variation1nstd209human GRCh38 chr9: 37,503,332-37,510,331 , GRCh37.p13 chr9: 37,503,329-37,510,328 FBXO10, POLR1E
    nsv5488072copy number variation1nstd206human GRCh38 chr9: 37,502,510-37,515,064 , GRCh37.p13 chr9: 37,502,507-37,515,061 POLR1E, FBXO10
    nsv5339288translocation1nstd200human GRCh37 chr9: 37,515,061-37,515,061 , GRCh37 chr9: 37,502,507-37,502,507 , GRCh38.p12 chr9: 37,502,510-37,502,510 , GRCh38.p12 chr9: 37,515,064-37,515,064 POLR1E, FBXO10
    nsv5305121copy number variation1nstd204human GRCh38.p13 chr9: 37,502,500-37,515,066 , GRCh37.p13 chr9: 37,502,497-37,515,063 FBXO10, POLR1E
    nsv5257242copy number variation1nstd204human GRCh38.p13 chr9: 37,502,420-37,517,470 , GRCh37.p13 chr9: 37,502,417-37,517,467 FBXO10, POLR1E
    nsv5246038copy number variation1nstd204human GRCh38.p13 chr9: 37,502,132-37,503,231 , GRCh37.p13 chr9: 37,502,129-37,503,228 POLR1E
    nsv4964395copy number variation1nstd200human GRCh38 chr9: 37,478,730-37,484,139 , GRCh37.p13 chr9: 37,478,727-37,484,136 POLR1E, KCTD9P3
    nsv4954686copy number variation1nstd200human GRCh38 chr9: 37,502,510-37,515,064 , GRCh37.p13 chr9: 37,502,507-37,515,061 POLR1E, FBXO10
    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
    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
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