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Items: 1 to 20 of 172

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6866300copy number variation1nstd229human GRCh38 chr9: 38,451,083-38,640,293 , GRCh37.p13 chr9: 38,451,080-38,640,290 FAM201A, ARMC8P1, 8 more genes
    nsv6862251copy number variation1nstd229human GRCh38 chr9: 38,498,789-38,685,383 , GRCh37.p13 chr9: 38,498,786-38,685,380 YWHABP1, ANKRD18A, 8 more genes
    nsv6858948copy number variation1nstd229human GRCh38 chr9: 37,926,854-38,721,465 , GRCh37.p13 chr9: 37,926,851-38,721,462 CYP4F33P, ANKRD18A, 19 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
    nsv6633518copy number variation1nstd224human GRCh37 chr9: 38,362,171-38,772,575 , GRCh38.p12 chr9: 38,362,174-38,772,578 FAM201A, ANKRD18A, 15 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
    nsv6276618insertion1nstd214human GRCh38 chr9: 38,620,520-38,620,520 , GRCh37.p13 chr9: 38,620,517-38,620,517 FAM201A, ANKRD18A
    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
    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
    nsv6137464copy number variation1nstd213human GRCh37 chr9: 37,180,000-39,190,001 , GRCh38.p12 chr9: 37,180,003-39,190,004 SHB, ZBTB5, 50 more genes
    nsv5490534copy number variation1nstd206human GRCh38 chr9: 38,498,789-38,685,381 , GRCh37.p13 chr9: 38,498,786-38,685,378 CYP4F33P, ANKRD18A, 8 more genes
    nsv4828338copy number variation1nstd200human GRCh37 chr9: 38,498,786-38,685,378 , GRCh38.p12 chr9: 38,498,789-38,685,381 ANKRD18A, YWHABP1, 8 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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