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Items: 1 to 20 of 354

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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
    nsv7097953copy number variation1nstd102humanUncertain significance GRCh37 chr9: 32,526,039-32,526,164 , GRCh38.p12 chr9: 32,526,041-32,526,166 RIGI
    nsv7097722copy number variation1nstd102humanUncertain significance GRCh37 chr9: 32,491,678-32,492,506 , GRCh38.p12 chr9: 32,491,680-32,492,508 RIGI
    nsv7097721copy number variation1nstd102humanUncertain significance GRCh37 chr9: 32,487,449-32,544,344 , GRCh38.p12 chr9: 32,487,451-32,544,346 RIGI, TOPORS
    nsv7070669inversion1nstd229human GRCh38 chr9: 32,475,163-32,483,314 , GRCh37.p13 chr9: 32,475,161-32,483,312 RIGI
    nsv7064944inversion1nstd229human GRCh38 chr9: 32,475,288-32,478,831 , GRCh37.p13 chr9: 32,475,286-32,478,829 RIGI
    nsv7063062inversion1nstd229human GRCh38 chr9: 22,592,329-32,576,343 , GRCh37.p13 chr9: 22,592,328-32,576,341 HSPA8P17, RMRPP5, 81 more genes
    nsv6875439copy number variation1nstd229human GRCh38 chr9: 32,502,107-32,502,136 , GRCh37.p13 chr9: 32,502,105-32,502,134 RIGI
    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
    nsv6869140copy number variation1nstd229human GRCh38 chr9: 32,499,811-32,509,182 , GRCh37.p13 chr9: 32,499,809-32,509,180 RIGI
    nsv6867883copy number variation1nstd229human GRCh38 chr9: 32,518,736-32,528,505 , GRCh37.p13 chr9: 32,518,734-32,528,503 RIGI
    nsv6862592copy number variation1nstd229human GRCh38 chr9: 32,478,832-32,482,997 , GRCh37.p13 chr9: 32,478,830-32,482,995 RIGI
    nsv6860825copy number variation1nstd229human GRCh38 chr9: 32,434,537-32,457,315 , GRCh37.p13 chr9: 32,434,535-32,457,313 RIGI, ACO1
    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
    nsv6572487inversion1nstd223human GRCh38 chr9: 32,481,871-32,482,751 , GRCh37.p13 chr9: 32,481,869-32,482,749 RIGI
    nsv6569028inversion1nstd223human GRCh38 chr9: 32,477,747-32,478,321 , GRCh37.p13 chr9: 32,477,745-32,478,319 RIGI
    nsv6565687inversion1nstd223human GRCh38 chr9: 32,498,705-32,499,521 , GRCh37.p13 chr9: 32,498,703-32,499,519 RIGI
    nsv6562741inversion1nstd223human GRCh38 chr9: 32,481,609-32,482,853 , GRCh37.p13 chr9: 32,481,607-32,482,851 RIGI
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