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Items: 1 to 20 of 339

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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
    nsv5880088copy number variation2nstd209human GRCh38 chr17: 18,418,523-18,423,080 , GRCh37.p13 chr17: 18,321,837-18,326,394 KRT17P5, YWHAEP2
    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
    nsv5294716copy number variation1nstd204human GRCh38.p13 chr17: 18,424,801-18,431,200 , GRCh37.p13 chr17: 18,328,115-18,334,514 KRT17P5, KRT17P2
    nsv5286974copy number variation1nstd204human GRCh38.p13 chr17: 18,418,523-18,423,080 , GRCh37.p13 chr17: 18,321,837-18,326,394 YWHAEP2, KRT17P5
    nsv5286642copy number variation1nstd204human GRCh38.p13 chr17: 18,424,497-18,425,820 , GRCh37.p13 chr17: 18,327,811-18,329,134 KRT17P5, KRT17P2
    nsv5283038copy number variation1nstd204human GRCh38.p13 chr17: 18,421,201-18,431,200 , GRCh37.p13 chr17: 18,324,515-18,334,514 KRT17P5, KRT17P2
    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
    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
    nsv4729738copy number variation1nstd102humanPathogenic GRCh37 chr17: 15,810,015-18,537,436 , GRCh38.p12 chr17: 15,906,701-18,634,123 UPF3AP1, ADORA2B, 109 more genes
    nsv4727893copy number variation3nstd197human GRCh37 chr17: 18,291,534-18,397,681 , GRCh38.p12 chr17: 18,388,220-18,494,367 , GRCh38.p12 chr17|NW_017363819.1: 158,199-264,346 TNPO1P2, KRT17P5, 10 more genes
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