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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6633539copy number variation1nstd224human GRCh37 chr9: 69,033,702-69,257,427 , GRCh38.p12 chr9: 40,960,473-41,184,198 LINC03025, PGM5P2, 5 more genes
    nsv6567122inversion1nstd223human GRCh38 chr9: 41,024,054-41,025,435 , GRCh37.p13 chr9: 69,097,283-69,098,664 FRG1HP, PGM5P2
    nsv6450733copy number variation1nstd223human GRCh38 chr9: 40,801,301-41,078,800 , GRCh37.p13 chr9: 68,664,183-68,814,085 PGM5P2, LOC107986997, 3 more genes
    nsv6449764copy number variation1nstd223human GRCh38 chr9: 40,861,801-41,113,400 , GRCh37.p13 chr9: 68,664,183-68,838,946 MIR1299, LINC03025, 4 more genes
    nsv6449211copy number variation1nstd223human GRCh38 chr9: 41,004,401-41,082,900 , GRCh37.p13 chr9: 69,077,630-69,156,129 PGM5P2, LOC105376058, 1 more genes
    nsv6445227copy number variation1nstd223human GRCh38 chr9: 40,876,369-41,152,593 , GRCh37.p13 chr9: 68,664,183-68,838,946 PGM5P2, FRG1HP, 6 more genes
    nsv6442902copy number variation1nstd223human GRCh38 chr9: 40,861,901-41,118,500 , GRCh37.p13 chr9: 68,664,183-68,838,946 LOC107986997, LINC03025, 4 more genes
    nsv6439498copy number variation1nstd223human GRCh38 chr9: 40,863,201-41,103,300 , GRCh37.p13 chr9: 68,664,183-68,838,633 LOC107986997, PGM5P2, 4 more genes
    nsv6439329copy number variation1nstd223human GRCh38 chr9: 41,004,301-41,082,900 , GRCh37.p13 chr9: 69,077,530-69,156,129 PGM5P2, LOC105376058, 1 more genes
    nsv6315415copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-68,342,786 , GRCh38.p12 chr9: 203,861-67,920,552 LOC107987068, FAM74A7, 846 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
    nsv6313827copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-84,155,399 , GRCh38.p12 chr9: 203,861-81,540,484 RPSAP75, ANKRD20A2P, 1008 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
    nsv6290004inversion1nstd102humanLikely pathogenic GRCh38.p12 chr9: 12,246,100-98,797,096 , GRCh37 chr9: 12,246,100-101,559,378 ACO1, PLIN2, 1215 more genes
    nsv6270000copy number variation1nstd214human GRCh38 chr9: 41,025,415-41,025,473 , GRCh37.p13 chr9: 69,098,644-69,098,702 FRG1HP, PGM5P2
    nsv6257652mobile element insertion1nstd215human GRCh38 chr9: 40,994,293-40,994,293 , GRCh37.p13 chr9: 69,067,522-69,067,522 FRG1HP
    nsv6142522copy number variation1nstd206human GRCh38 chr9: 40,561,974-41,135,974 , GRCh37.p13 chr: NaN-NaN IGKV1OR9-2, FOXD4L6, 14 more genes
    nsv6087570insertion1nstd212human GRCh38 chr9: 41,025,431-41,025,431 , GRCh37.p13 chr9: 69,098,660-69,098,660 FRG1HP, PGM5P2
    nsv6083451insertion1nstd212human GRCh38 chr9: 40,991,811-40,991,811 , GRCh37.p13 chr9: 69,065,040-69,065,040 LOC107986997, FRG1HP
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