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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098455copy number variation6nstd102humanUncertain significance GRCh37 chr9: 32,453,279-37,785,041 , GRCh38.p12 chr9: 32,453,281-37,785,044 TRBVAOR9-2, UBAP2, 197 more genes
    nsv7098080copy number variation1nstd102humanUncertain significance GRCh37 chr9: 32,453,279-35,068,379 , GRCh38.p12 chr9: 32,453,281-35,068,382 SUGT1P1, RNU7-36P, 110 more genes
    nsv7061538inversion1nstd229human GRCh38 chr9: 32,629,662-32,752,370 , GRCh37.p13 chr9: 32,629,660-32,752,368 SNRPCP1, LOC105376016, 3 more genes
    nsv6872931copy number variation1nstd229human GRCh38 chr9: 29,015,647-32,650,007 , GRCh37.p13 chr9: 29,015,645-32,650,005 NDUFB6, LOC105376011, 32 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
    nsv6634409copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 1-40,036,525 , GRCh38.p12 chr9: 10,001-39,445,729 ACO1, PLIN2, 594 more genes
    nsv6315463copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-35,903,398 , GRCh38.p12 chr9: 203,861-35,903,401 IFNA11P, RNU6-14P, 495 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
    nsv6313892copy number variation1nstd102humanPathogenic GRCh37 chr9: 676,264-33,743,670 , GRCh38.p12 chr9: 676,264-33,743,672 SUGT1P1, FOCAD-AS1, 391 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
    nsv6142382copy number variation1nstd206human GRCh38 chr9: 32,548,142-32,641,173 , GRCh37.p13 chr9: 32,548,140-32,641,171 NDUFB6, TOPORS, 4 more genes
    nsv6137461copy number variation1nstd213human GRCh37 chr9: 32,140,000-33,310,001 , GRCh38.p12 chr9: 32,140,002-33,310,003 ACO1, BAG1, 31 more genes
    nsv6137089copy number variation1nstd213human GRCh37 chr9: 32,230,000-34,220,001 , GRCh38.p12 chr9: 32,230,002-34,220,003 ANXA2P2, TRBV21OR9-2, 75 more genes
    nsv6137086copy number variation1nstd213human GRCh37 chr9: 29,710,000-37,450,001 , GRCh38.p12 chr9: 29,710,002-37,450,004 AQP7, BAG1, 210 more genes
    nsv5381740copy number variation1nstd102humanUncertain significance GRCh37 chr9: 32,399,559-33,541,225 , GRCh38.p12 chr9: 32,399,561-33,541,227 SMU1, RNU4ATAC15P, 38 more genes
    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
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