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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5711909mobile element insertion1nstd211human GRCh38 chr17: 18,425,014-18,425,014 , GRCh37.p13 chr17: 18,328,328-18,328,328 KRT17P5, KRT17P2
    nsv5665112inversion1nstd207human GRCh37.p13 chr17: 16,704,599-18,417,421 , GRCh38 chr17: 16,801,285-18,514,107 , DRG2, 71 more genes
    nsv5421739mobile element insertion1nstd206human GRCh38 chr17: 18,425,014-18,425,065 , GRCh37.p13 chr17: 18,328,328-18,328,379 KRT17P2, KRT17P5
    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
    nsv5298791copy number variation1nstd204human GRCh38.p13 chr17: 18,430,501-18,431,400 , GRCh37.p13 chr17: 18,333,815-18,334,714 KRT17P2
    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
    nsv5297196copy number variation1nstd204human GRCh38.p13 chr17: 18,428,446-18,429,939 , GRCh37.p13 chr17: 18,331,760-18,333,253 KRT17P2
    nsv5295492copy number variation1nstd204human GRCh38.p13 chr17: 18,426,701-18,433,200 , GRCh37.p13 chr17: 18,330,015-18,336,514 KRT17P2
    nsv5294716copy number variation1nstd204human GRCh38.p13 chr17: 18,424,801-18,431,200 , GRCh37.p13 chr17: 18,328,115-18,334,514 KRT17P5, KRT17P2
    nsv5291471copy number variation1nstd204human GRCh38.p13 chr17: 18,426,901-18,428,700 , GRCh37.p13 chr17: 18,330,215-18,332,014 KRT17P2
    nsv5286642copy number variation1nstd204human GRCh38.p13 chr17: 18,424,497-18,425,820 , GRCh37.p13 chr17: 18,327,811-18,329,134 KRT17P5, KRT17P2
    nsv5286622copy number variation1nstd204human GRCh38.p13 chr17: 18,428,101-18,430,200 , GRCh37.p13 chr17: 18,331,415-18,333,514 KRT17P2
    nsv5283038copy number variation1nstd204human GRCh38.p13 chr17: 18,421,201-18,431,200 , GRCh37.p13 chr17: 18,324,515-18,334,514 KRT17P5, KRT17P2
    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
    nsv5151566mobile element insertion1nstd203human GRCh38 chr17: 18,425,000-18,425,014 , GRCh37.p13 chr17: 18,328,314-18,328,328 KRT17P2, KRT17P5
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
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