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Items: 1 to 20 of 222

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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
    nsv7063062inversion1nstd229human GRCh38 chr9: 22,592,329-32,576,343 , GRCh37.p13 chr9: 22,592,328-32,576,341 HSPA8P17, RMRPP5, 81 more genes
    nsv6874273copy number variation1nstd229human GRCh38 chr9: 32,553,106-32,553,130 , GRCh37.p13 chr9: 32,553,104-32,553,128 SMIM27, TOPORS, 1 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
    nsv6870682copy number variation1nstd229human GRCh38 chr9: 32,560,560-32,566,554 , GRCh37.p13 chr9: 32,560,558-32,566,552 SMIM27, NDUFB6, 1 more genes
    nsv6864951copy number variation1nstd229human GRCh38 chr9: 32,560,104-32,561,147 , GRCh37.p13 chr9: 32,560,102-32,561,145 NDUFB6, SMIM27
    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
    nsv6446243copy number variation1nstd223human GRCh38 chr9: 32,560,104-32,561,147 , GRCh37.p13 chr9: 32,560,102-32,561,145 SMIM27, NDUFB6
    nsv6443868copy number variation1nstd223human GRCh38 chr9: 32,560,800-32,566,595 , GRCh37.p13 chr9: 32,560,798-32,566,593 SMIM27, DFFBP1, 1 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
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