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Items: 1 to 20 of 812

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137216copy number variation1nstd102humanPathogenic GRCh37 chr17: 30,572,862-35,843,988 , GRCh38.p12 chr17: 32,245,843-36,446,544 PSMD11, C17orf50, 117 more genes
    nsv7098907copy number variation1nstd102humanPathogenic GRCh38 chr17: 36,138,501-37,924,067 , GRCh37.p13 chr17: 34,900,240-35,888,667 LOC102723414, SYNRG, 51 more genes
    nsv7073998inversion1nstd229human GRCh38 chr17: 32,918,710-41,148,753 , GRCh37.p13 chr17: 31,245,728-39,305,005 LOC105371750, C17orf78, 298 more genes
    nsv6637369copy number variation1nstd102humanPathogenic GRCh37 chr17: 34,425,363-36,404,555 , GRCh38.p12 chr17|NT_187614.1: 332,891-2,283,620 CCL3L3, MRM1, 63 more genes
    nsv6624271copy number variation1nstd224human GRCh37 chr17: 34,391,721-34,819,750 , GRCh38.p12 chr17|NT_187614.1: 299,249-698,812 LOC101060212, LOC101927369, 20 more genes
    nsv6512549copy number variation1nstd223human GRCh38 chr17: 36,189,801-36,236,400 , GRCh37.p13 chr17|NW_003315949.1: 74,557-121,156 , LOC105371747, 2 more genes
    nsv6508750copy number variation1nstd223human GRCh38 chr17: 36,192,301-36,228,100 , GRCh37.p13 chr17|NW_003315949.1: 77,057-112,856 , LOC105371747, 2 more genes
    nsv6507521copy number variation1nstd223human GRCh38 chr17: 36,190,301-36,240,500 , GRCh37.p13 chr17|NW_003315949.1: 75,057-125,256 , CCL4L2, 2 more genes
    nsv6505903copy number variation1nstd223human GRCh38 chr17: 36,198,701-36,222,200 , GRCh37.p13 chr17|NW_003315949.1: 83,457-106,956 , CCL4L2
    nsv6504428copy number variation1nstd223human GRCh38 chr17: 36,208,101-36,228,600 , GRCh37.p13 chr17|NW_003315949.1: 92,857-113,356 , LOC105371747, 1 more genes
    nsv6504276copy number variation1nstd223human GRCh38 chr17: 36,209,201-36,215,400 , GRCh37.p13 chr17|NW_003315949.1: 93,957-100,156 , CCL4L2
    nsv6503336copy number variation1nstd223human GRCh38 chr17: 36,190,801-36,229,400 , GRCh37.p13 chr17|NW_003315949.1: 75,557-114,156 , CCL3L3, 2 more genes
    nsv6501760copy number variation1nstd223human GRCh38 chr17: 36,190,201-36,225,800 , GRCh37.p13 chr17|NW_003315949.1: 74,957-110,556 , LOC105371747, 2 more genes
    nsv6500452copy number variation1nstd223human GRCh38 chr17: 36,209,401-36,214,800 , GRCh37.p13 chr17|NW_003315949.1: 94,157-99,556 , CCL4L2
    nsv6499200copy number variation1nstd223human GRCh38 chr17: 36,209,301-36,229,600 , GRCh37.p13 chr17|NW_003315949.1: 94,057-114,356 , LOC105371747, 1 more genes
    nsv6495692copy number variation1nstd223human GRCh38 chr17: 36,168,964-36,453,032 , GRCh37.p13 chr17|NW_003315949.1: 53,702-337,782 , TBC1D3I, 13 more genes
    nsv6315528copy number variation1nstd102humanPathogenic GRCh37 chr17: 34,463,923-36,410,559 , GRCh38.p12 chr17|NT_187614.1: 371,451-2,289,624 LOC105371750, DDX52, 60 more genes
    nsv6145850copy number variation1nstd206human GRCh38 chr17: 36,095,490-38,260,000 , GRCh37.p13 chr17: 34,422,828-36,416,003 , PIGW, 70 more genes
    nsv6090205insertion1nstd212human GRCh38 chr17: 36,213,371-36,213,371 , GRCh37.p13 chr17|NW_003315949.1: 98,127-98,127 , CCL4L2
    nsv5882424copy number variation6nstd209human GRCh38 chr17: 36,205,445-36,220,260 , GRCh37.p13 chr17|NW_003315949.1: 90,201-105,016 , CCL4L2
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