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Items: 1 to 20 of 163

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144856copy number variation1nstd232human GRCh37.p13 chr7: 107,559,543-107,559,636 , GRCh38.p12 chr7: 107,919,098-107,919,191 DLD
    nsv7144669insertion1nstd232human GRCh37.p13 chr7: 107,531,735-107,531,735 , GRCh38.p12 chr7: 107,891,290-107,891,290 DLD
    nsv7097853copy number variation1nstd102humanPathogenic GRCh37 chr7: 104,456,677-108,155,935 , GRCh38.p12 chr7: 104,816,230-108,515,491 RNU6-1322P, COG5, 57 more genes
    nsv7097603copy number variation1nstd102humanPathogenic GRCh37 chr7: 107,412,489-107,559,714 , GRCh38.p12 chr7: 107,772,044-107,919,269 LOC105375444, DLD, 3 more genes
    nsv7097099copy number variation1nstd102humanUncertain significance GRCh37 chr7: 102,937,907-107,643,330 , GRCh38.p12 chr7: 103,297,460-108,002,885 SRPK2, SYPL1, 60 more genes
    nsv6834035copy number variation1nstd229human GRCh38 chr7: 107,901,921-107,902,055 , GRCh37.p13 chr7: 107,542,366-107,542,500 DLD
    nsv6831951copy number variation1nstd229human GRCh38 chr7: 107,606,801-107,918,600 , GRCh37.p13 chr7: 107,247,246-107,559,045 WBP1LP2, SLC26A4-AS1, 11 more genes
    nsv6831305copy number variation1nstd229human GRCh38 chr7: 107,904,737-107,910,624 , GRCh37.p13 chr7: 107,545,182-107,551,069 DLD
    nsv6828603copy number variation1nstd229human GRCh38 chr7: 107,770,269-108,588,414 , GRCh37.p13 chr7: 107,410,714-108,228,858 LOC105375444, DLD, 15 more genes
    nsv6823010copy number variation1nstd229human GRCh38 chr7: 107,877,608-108,004,972 , GRCh37.p13 chr7: 107,518,053-107,645,417 LAMB1, DLD
    nsv6821600copy number variation1nstd229human GRCh38 chr7: 107,920,401-108,118,100 , GRCh37.p13 chr7: 107,560,846-107,758,545 LOC107986834, LAMB1, 4 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6617177copy number variation1nstd223human GRCh38 chr7: 107,910,501-107,911,700 , GRCh37.p13 chr7: 107,550,946-107,552,145 DLD
    nsv6603941copy number variation1nstd223human GRCh38 chr7: 107,913,301-107,914,800 , GRCh37.p13 chr7: 107,553,746-107,555,245 DLD
    nsv6603426copy number variation1nstd223human GRCh38 chr7: 107,881,201-107,893,700 , GRCh37.p13 chr7: 107,521,646-107,534,145 DLD
    nsv6602241copy number variation1nstd223human GRCh38 chr7: 107,903,150-107,912,065 , GRCh37.p13 chr7: 107,543,595-107,552,510 DLD
    nsv6562778inversion1nstd223human GRCh38 chr7: 107,908,435-107,908,723 , GRCh37.p13 chr7: 107,548,880-107,549,168 DLD
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313851copy number variation1nstd102humanPathogenic GRCh37 chr7: 106,984,287-128,949,489 , GRCh38.p12 chr7: 107,343,842-129,309,648 DOCK4-AS1, RPL3P8, 262 more genes
    nsv6313576copy number variation1nstd102humanPathogenic GRCh37 chr7: 100,676,872-119,156,160 , GRCh38.p12 chr7: 101,033,591-119,516,106 LHFPL3-AS2, CTB-30L5.1, 233 more genes
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