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Items: 1 to 20 of 353

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6128056copy number variation1nstd186human GRCh37 chr17: 18,340,425-18,466,064 , GRCh38.p12 chr17|NW_017363819.1: 207,090-276,292 , GRCh38.p12 chr17: 18,437,111-18,562,750 LOC105371570, FAM106A, 9 more genes
    nsv5974534inversion1nstd209human GRCh38 chr17: 15,750,079-18,634,890 , GRCh37.p13 chr17: 15,653,393-18,538,203 , ADORA2B, 119 more genes
    nsv5933579copy number variation1nstd209human GRCh38 chr17: 16,936,959-20,558,118 , GRCh37.p13 chr17: 16,840,273-20,461,431 , FAM106B, 146 more genes
    nsv5930475copy number variation1nstd209human GRCh38 chr17: 18,416,368-18,545,712 , GRCh37.p13 chr17: 18,319,682-18,449,026 LOC105371570, TNPO1P2, 12 more genes
    nsv5665112inversion1nstd207human GRCh37.p13 chr17: 16,704,599-18,417,421 , GRCh38 chr17: 16,801,285-18,514,107 , DRG2, 71 more genes
    nsv5527136copy number variation1nstd206human GRCh38 chr17: 18,437,111-18,562,750 , GRCh37.p13 chr17: 18,340,425-18,466,064 LOC105371569, KRT16P4, 9 more genes
    nsv5381800copy number variation1nstd102humanPathogenic GRCh37 chr17: 16,601,603-20,063,369 , GRCh38.p12 chr17: 16,698,289-20,160,056 COTL1P1, LOC105371551, 141 more genes
    nsv5381797copy number variation1nstd102humanPathogenic GRCh37 chr17: 17,145,361-20,137,943 , GRCh38.p12 chr17: 17,242,047-20,234,630 LOC644909, FLII, 117 more genes
    nsv5299601copy number variation1nstd204human GRCh38.p13 chr17: 18,434,101-18,442,400 , GRCh37.p13 chr17: 18,337,415-18,345,714 LOC105371570, LOC105371569, 1 more genes
    nsv5298000copy number variation1nstd204human GRCh38.p13 chr17: 18,427,101-18,442,400 , GRCh37.p13 chr17: 18,330,415-18,345,714 KRT16P1, KRT17P2, 2 more genes
    nsv5288806copy number variation1nstd204human GRCh38.p13 chr17: 18,438,701-18,439,200 , GRCh37.p13 chr17: 18,342,015-18,342,514 LOC105371570, KRT16P1
    nsv5287709copy number variation1nstd204human GRCh38.p13 chr17: 18,436,801-18,459,000 , GRCh37.p13 chr17: 18,340,115-18,362,314 KRT16P1, LOC105371569, 3 more genes
    nsv5287186copy number variation1nstd204human GRCh38.p13 chr17: 18,438,101-18,444,800 , GRCh37.p13 chr17: 18,341,415-18,348,114 LOC105371570, KRT16P1, 1 more genes
    nsv5282453copy number variation1nstd204human GRCh37.p13 chr17: 18,331,415-18,362,314 , GRCh38.p13 chr17: 18,428,101-18,459,000 TNPO1P2, KRT17P2, 4 more genes
    nsv5282347copy number variation1nstd204human GRCh38.p13 chr17: 18,441,201-18,442,400 , GRCh37.p13 chr17: 18,344,515-18,345,714 KRT16P1, LOC105371569
    nsv5280811copy number variation1nstd204human GRCh38.p13 chr17: 18,440,001-18,442,400 , GRCh37.p13 chr17: 18,343,315-18,345,714 LOC105371570, KRT16P1, 1 more genes
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4730068inversion20nstd198human GRCh37.p13 chr17: 18,312,480-18,778,530 , GRCh38 chr17: 18,409,166-18,875,217 FOXO3B, PRPSAP2, 26 more genes
    nsv4729886copy number variation1nstd102humanPathogenic GRCh37 chr17: 16,763,370-20,395,611 , GRCh38.p12 chr17: 16,860,056-20,492,298 LOC100419620, PAIP1P2, 139 more genes
    nsv4729810copy number variation1nstd102humanPathogenic GRCh37 chr17: 16,761,814-20,330,062 , GRCh38.p12 chr17: 16,858,500-20,426,749 PRPSAP2, EPN2, 134 more genes
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