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Items: 1 to 20 of 110

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6637259copy number variation1nstd102humanUncertain significance GRCh37 chr9: 84,027,223-84,848,369 , GRCh38.p12 chr9: 81,412,308-82,233,454 SPATA31D1, SPATA31D2P, 13 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
    nsv6568042inversion1nstd223human GRCh38 chr9: 77,399,209-87,276,767 , GRCh37.p13 chr9: 80,014,125-89,891,682 , LOC105376119, 118 more genes
    nsv6557715inversion1nstd223human GRCh38 chr9: 75,901,418-82,872,806 , GRCh37.p13 chr9: 78,516,334-85,487,721 , LOC105376096, 79 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
    nsv6313900copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 71,349,994-122,603,410 , GRCh38.p12 chr9: 68,735,078-119,841,132 ABCA1, ALAD, 793 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
    nsv6137096copy number variation1nstd213human GRCh37 chr9: 84,500,000-85,200,001 , GRCh38.p12 chr9: 81,885,085-82,585,086 , SPATA31D5P, 16 more genes
    nsv5867333copy number variation1nstd209human GRCh38 chr9: 81,994,737-81,996,737 , GRCh37.p13 chr9: 84,609,652-84,611,652 LOC105376107, SPATA31D1
    nsv5863726copy number variation1nstd209human GRCh38 chr9: 81,977,013-81,993,286 , GRCh37.p13 chr9: 84,591,928-84,608,201 , SPATA31D1, 1 more genes
    nsv5853024copy number variation1nstd209human GRCh38 chr9: 81,983,701-81,986,073 , GRCh37.p13 chr9: 84,598,616-84,600,988 SPATA31D1, LOC105376107
    nsv5847989copy number variation1nstd209human GRCh38 chr9: 81,983,702-82,001,771 , GRCh37.p13 chr9: 84,598,617-84,616,686 SPATA31D1, LOC105376107
    nsv5710231mobile element insertion1nstd211human GRCh38 chr9: 81,987,801-81,987,801 , GRCh37.p13 chr9: 84,602,716-84,602,716 SPATA31D1, LOC105376107
    nsv5603917copy number variation1nstd207human GRCh38 chr9: 81,988,169-81,992,901 , GRCh37.p13 chr9: 84,603,084-84,607,816 LOC105376107, SPATA31D1
    nsv5130152mobile element insertion1nstd203human GRCh38 chr9: 81,987,787-81,987,801 , GRCh37.p13 chr9: 84,602,702-84,602,716 SPATA31D1, LOC105376107
    nsv5036269inversion1nstd200human GRCh38 chr9: 79,108,237-87,224,469 , GRCh37.p13 chr9: 81,723,153-89,839,384 , RMI1, 100 more genes
    nsv4498271mobile element insertion1nstd166human GRCh37.p13 chr9: 84,602,702-84,602,702 , GRCh38.p12 chr9: 81,987,787-81,987,787 SPATA31D1, LOC105376107
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
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