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Items: 1 to 20 of 127

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099235copy number variation1nstd231human GRCh38.p12 chr1: 154,116,919-155,715,830 , GRCh37 chr1: 154,089,395-155,685,621 ADAR, CHRNB2, 80 more genes
    nsv7095320copy number variation1nstd102humanPathogenic GRCh37 chr1: 153,963,273-154,580,482 , GRCh38.p12 chr1: 153,990,797-154,608,006 RNU6-239P, ATP8B2, 30 more genes
    nsv7056666inversion1nstd229human GRCh38 chr1: 151,403,323-155,722,147 , GRCh37.p13 chr1: 151,375,799-155,691,938 ILF2, SPRR2C, 219 more genes
    nsv7044458inversion1nstd229human GRCh38 chr1: 150,355,899-155,246,175 , GRCh37.p13 chr1: 150,440,214-155,215,966 LCE2C, MUC1, 254 more genes
    nsv7042502inversion1nstd229human GRCh38 chr1: 150,301,267-155,517,761 , GRCh37.p13 chr1: 150,440,214-155,487,552 LINGO4, CELF3, 268 more genes
    nsv7041246inversion1nstd229human GRCh38 chr1: 153,232,460-155,277,038 , GRCh37.p13 chr1: 153,204,936-155,246,829 INTS3, GBA1LP, 111 more genes
    nsv6642697copy number variation1nstd229human GRCh38 chr1: 154,406,208-154,416,796 , GRCh37.p13 chr1: 154,378,684-154,389,272 PSMD8P1, IL6R-AS1, 1 more genes
    nsv6635920copy number variation1nstd227human GRCh38.p12 chr1: 154,398,462-154,405,422 , GRCh37 chr1: 154,370,938-154,377,898 IL6R, IL6R-AS1
    nsv6310678copy number variation4nstd102humanUncertain significance GRCh37 chr1: 149,895,434-156,851,434 , GRCh38.p12 chr1: 149,923,542-156,881,642 PRPF3, KHDC4, 352 more genes
    nsv6310523copy number variation1nstd102humanUncertain significance GRCh37 chr1: 154,141,761-156,851,434 , GRCh38.p12 chr1: 154,169,285-156,881,642 MIR555, CFAP141, 135 more genes
    nsv6133737copy number variation1nstd213human GRCh37 chr1: 153,820,000-155,320,001 , GRCh38.p12 chr1: 153,847,524-155,350,210 GBA1LP, PKLR, 81 more genes
    nsv6133734copy number variation1nstd213human GRCh37 chr1: 150,350,000-154,440,001 , GRCh38.p12 chr1: 150,377,524-154,467,525 , MCL1, 216 more genes
    nsv6133560copy number variation1nstd213human GRCh37 chr1: 153,460,000-155,250,001 , GRCh38.p12 chr1: 153,487,524-155,280,210 CKS1B, ILF2, 97 more genes
    nsv5610091insertion1nstd207human GRCh38 chr1: 154,402,391-154,402,391 , GRCh37.p13 chr1: 154,374,867-154,374,867 IL6R-AS1
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5211686copy number variation1nstd204human GRCh38.p13 chr1: 153,974,901-155,189,600 , GRCh37.p13 chr1: 153,947,377-155,161,231 JTB, PYGO2-AS1, 56 more genes
    nsv5194314mobile element insertion1nstd203human GRCh38 chr1: 154,402,397-154,402,406 , GRCh37.p13 chr1: 154,374,873-154,374,882 IL6R-AS1
    nsv5193445mobile element insertion1nstd203human GRCh38 chr1: 154,402,390-154,402,406 , GRCh37.p13 chr1: 154,374,866-154,374,882 IL6R-AS1
    nsv5187452mobile element insertion1nstd203human GRCh38 chr1: 154,402,391-154,402,406 , GRCh37.p13 chr1: 154,374,867-154,374,882 IL6R-AS1
    nsv5186275mobile element insertion1nstd203human GRCh38 chr1: 154,402,394-154,402,401 , GRCh37.p13 chr1: 154,374,870-154,374,877 IL6R-AS1
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