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Items: 1 to 20 of 225

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5937790copy number variation1nstd209human GRCh38 chr17: 30,668,045-32,084,125 , GRCh37.p13 chr17: 28,995,063-30,411,144 , OMG, 39 more genes
    nsv5937217copy number variation1nstd209human GRCh38 chr17: 30,601,695-31,009,572 , GRCh37.p13 chr17: 28,928,713-29,336,590 LOC107984974, CRLF3, 16 more genes
    nsv5585170copy number variation1nstd207human GRCh38 chr17: 30,859,685-30,860,047 , GRCh37.p13 chr17: 29,186,703-29,187,065 RNU6-298P, ATAD5
    nsv5391947copy number variation1nstd186human GRCh37 chr17: 29,186,714-29,187,073 , GRCh38.p12 chr17: 30,859,696-30,860,055 RNU6-298P, ATAD5
    nsv5383967mobile element deletion1nstd186human GRCh37 chr17: 29,186,735-29,187,034 , GRCh38.p12 chr17: 30,859,717-30,860,016 ATAD5, RNU6-298P
    nsv5299152copy number variation1nstd204human GRCh38.p13 chr17: 30,850,901-30,919,000 , GRCh37.p13 chr17: 29,177,919-29,246,018 ATAD5, RNU6-298P, 1 more genes
    nsv5295965copy number variation1nstd204human GRCh38.p13 chr17: 30,859,701-30,860,000 , GRCh37.p13 chr17: 29,186,719-29,187,018 RNU6-298P, ATAD5
    nsv5289655copy number variation1nstd204human GRCh37.p13 chr17: 28,976,919-29,216,418 , GRCh38.p13 chr17: 30,649,901-30,889,400 CRLF3, ATAD5, 5 more genes
    nsv5212667mobile element deletion1nstd204human GRCh37.p13 chr17: 29,186,503-29,187,254 , GRCh38.p13 chr17: 30,859,485-30,860,236 ATAD5, RNU6-298P
    nsv5010360copy number variation1nstd200human GRCh38 chr17: 30,860,081-30,863,101 , GRCh37.p13 chr17: 29,187,099-29,190,119 ATAD5, RNU6-298P
    nsv5010359copy number variation1nstd200human GRCh38 chr17: 30,859,641-30,860,095 , GRCh37.p13 chr17: 29,186,659-29,187,113 RNU6-298P, ATAD5
    nsv4858551copy number variation1nstd200human GRCh37 chr17: 29,187,099-29,190,119 , GRCh38.p12 chr17: 30,860,081-30,863,101 RNU6-298P, ATAD5
    nsv4769483mobile element deletion1nstd200human GRCh37 chr17: 29,186,648-29,187,124 , GRCh38.p12 chr17: 30,859,630-30,860,106 RNU6-298P, ATAD5
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4737839copy number variation1nstd199human GRCh37 chr17: 29,186,674-29,187,035 , GRCh38.p12 chr17: 30,859,656-30,860,017 ATAD5, RNU6-298P
    nsv4729986copy number variation1nstd102humanUncertain significance GRCh37 chr17: 28,931,870-29,336,853 , GRCh38.p12 chr17: 30,604,852-31,009,835 RN7SL138P, LOC107984974, 16 more genes
    nsv4729791copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,039,844-30,412,788 , GRCh38.p12 chr17: 30,712,826-32,085,769 ADAP2, TEFM, 37 more genes
    nsv4729745copy number variation1nstd102humanUncertain significance GRCh37 chr17: 29,061,631-29,305,516 , GRCh38.p12 chr17: 30,734,613-30,978,498 SUZ12P1, RPS17P3, 8 more genes
    nsv4675286copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,088,218-30,159,137 , GRCh38.p12 chr17: 30,761,200-31,832,118 CRLF3, RN7SL45P, 30 more genes
    nsv4654161copy number variation1nstd186human GRCh37 chr17: 29,186,736-29,187,034 , GRCh38.p12 chr17: 30,859,718-30,860,016 ATAD5, RNU6-298P
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