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Items: 1 to 20 of 303

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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
    nsv5869032copy number variation1nstd209human GRCh38 chr17: 18,227,959-18,228,958 , GRCh37.p13 chr17: 18,131,273-18,132,272 LLGL1
    nsv5696731mobile element insertion1nstd211human GRCh38 chr17: 18,244,746-18,244,746 , GRCh37.p13 chr17: 18,148,060-18,148,060 LLGL1, FLII
    nsv5665112inversion1nstd207human GRCh37.p13 chr17: 16,704,599-18,417,421 , GRCh38 chr17: 16,801,285-18,514,107 , DRG2, 71 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
    nsv5026148copy number variation1nstd200human GRCh38 chr17: 18,243,296-18,244,455 , GRCh37.p13 chr17: 18,146,610-18,147,769 LLGL1, FLII
    nsv5023732copy number variation1nstd200human GRCh38 chr17: 18,206,397-18,233,822 , GRCh37.p13 chr17: 18,109,711-18,137,136 LLGL1, ALKBH5
    nsv4858262copy number variation1nstd200human GRCh37 chr17: 18,146,610-18,147,769 , GRCh38.p12 chr17: 18,243,296-18,244,455 , GRCh38.p12 chr17|NW_017363819.1: 3,670-4,829 LLGL1, FLII
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4729922copy number variation1nstd102humanUncertain significance GRCh37 chr17: 18,125,256-18,304,190 , GRCh38.p12 chr17: 18,221,942-18,400,876 , GRCh38.p12 chr17|NW_017363819.1: 1-170,855 RPL21P121, EVPLL, 9 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
    nsv4675003copy number variation1nstd102humanPathogenic GRCh37 chr17: 15,632,431-18,726,389 , GRCh38.p12 chr17: 15,729,117-18,823,076 LLGL1, LOC107985051, 127 more genes
    nsv4634335copy number variation1nstd183human GRCh37 chr17: 18,128,439-18,129,535 , GRCh38.p12 chr17: 18,225,125-18,226,221 LLGL1
    nsv4620518copy number variation1nstd183human GRCh37 chr17: 18,128,979-18,129,082 , GRCh38.p12 chr17: 18,225,665-18,225,768 LLGL1
    nsv4436751copy number variation1nstd102humanPathogenic GRCh37 chr17: 16,908,991-18,322,254 , GRCh38.p12 chr17: 17,005,677-18,418,940 RPL7AP65, TOP3A, 46 more genes
    nsv4349342copy number variation1nstd102humanPathogenic GRCh37 chr17: 16,842,991-20,217,316 , GRCh38.p12 chr17: 16,939,677-20,314,003 LOC105371566, LOC105371569, 126 more genes
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