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Items: 1 to 20 of 609

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097677copy number variation1nstd102humanPathogenic GRCh37 chr9: 104,124,710-104,500,261 , GRCh38.p12 chr9: 101,362,428-101,737,979 TMEM246-AS1, PGAP4, 10 more genes
    nsv7066403inversion1nstd229human GRCh38 chr9: 101,622,711-101,622,775 , GRCh37.p13 chr9: 104,384,993-104,385,057 GRIN3A
    nsv6877550copy number variation1nstd229human GRCh38 chr9: 101,604,843-101,625,686 , GRCh37.p13 chr9: 104,367,125-104,387,968 GRIN3A
    nsv6877015copy number variation1nstd229human GRCh38 chr9: 101,712,080-101,717,240 , GRCh37.p13 chr9: 104,474,362-104,479,522 GRIN3A
    nsv6872316copy number variation1nstd229human GRCh38 chr9: 101,735,197-101,735,861 , GRCh37.p13 chr9: 104,497,479-104,498,143 GRIN3A
    nsv6871366copy number variation1nstd229human GRCh38 chr9: 101,710,276-101,716,441 , GRCh37.p13 chr9: 104,472,558-104,478,723 GRIN3A
    nsv6868875copy number variation1nstd229human GRCh38 chr9: 101,734,419-101,735,937 , GRCh37.p13 chr9: 104,496,701-104,498,219 GRIN3A
    nsv6868418copy number variation1nstd229human GRCh38 chr9: 101,302,335-101,603,079 , GRCh37.p13 chr9: 104,064,617-104,365,361 RNF20, PLPPR1, 14 more genes
    nsv6868344copy number variation1nstd229human GRCh38 chr9: 101,703,015-101,703,204 , GRCh37.p13 chr9: 104,465,297-104,465,486 GRIN3A
    nsv6867731copy number variation1nstd229human GRCh38 chr9: 101,737,755-101,737,795 , GRCh37.p13 chr9: 104,500,037-104,500,077 GRIN3A
    nsv6867133copy number variation1nstd229human GRCh38 chr9: 101,645,201-101,675,300 , GRCh37.p13 chr9: 104,407,483-104,437,582 GRIN3A
    nsv6865292copy number variation1nstd229human GRCh38 chr9: 101,640,001-101,646,400 , GRCh37.p13 chr9: 104,402,283-104,408,682 GRIN3A
    nsv6861965copy number variation1nstd229human GRCh38 chr9: 101,661,270-101,665,284 , GRCh37.p13 chr9: 104,423,552-104,427,566 GRIN3A
    nsv6861407copy number variation1nstd229human GRCh38 chr9: 101,590,393-101,590,427 , GRCh37.p13 chr9: 104,352,675-104,352,709 GRIN3A, PPP3R2
    nsv6860951copy number variation1nstd229human GRCh38 chr9: 101,681,697-101,682,445 , GRCh37.p13 chr9: 104,443,979-104,444,727 GRIN3A
    nsv6860397copy number variation1nstd229human GRCh38 chr9: 101,549,595-101,841,268 , GRCh37.p13 chr9: 104,311,877-104,603,550 GRIN3A, LOC105376186, 4 more genes
    nsv6859660copy number variation1nstd229human GRCh38 chr9: 101,582,018-101,584,360 , GRCh37.p13 chr9: 104,344,300-104,346,642 GRIN3A
    nsv6859355copy number variation1nstd229human GRCh38 chr9: 101,628,401-101,631,500 , GRCh37.p13 chr9: 104,390,683-104,393,782 GRIN3A
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6561154inversion1nstd223human GRCh38 chr9: 101,587,203-101,589,213 , GRCh37.p13 chr9: 104,349,485-104,351,495 GRIN3A
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