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Items: 1 to 20 of 143

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099234copy number variation1nstd231human GRCh38.p12 chr1: 153,531,288-153,715,568 , GRCh37 chr1: 153,503,764-153,688,044 ILF2, NPR1, 16 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
    nsv6642440copy number variation1nstd229human GRCh38 chr1: 153,657,416-153,660,587 , GRCh37.p13 chr1: 153,629,892-153,633,063 SNAPIN, ILF2
    nsv6642437copy number variation1nstd229human GRCh38 chr1: 153,574,701-154,062,600 , GRCh37.p13 chr1: 153,547,177-154,035,076 S100A13, S100A16, 27 more genes
    nsv6642234copy number variation1nstd229human GRCh38 chr1: 153,624,501-153,754,300 , GRCh37.p13 chr1: 153,596,977-153,726,776 TRX-CAT1-1, INTS3, 9 more genes
    nsv6641990copy number variation1nstd229human GRCh38 chr1: 153,661,201-153,690,400 , GRCh37.p13 chr1: 153,633,677-153,662,876 NPR1, ILF2, 3 more genes
    nsv6334235copy number variation1nstd223human GRCh38 chr1: 153,655,301-153,657,000 , GRCh37.p13 chr1: 153,627,777-153,629,476 SNAPIN
    nsv6332425copy number variation1nstd223human GRCh38 chr1: 153,638,917-153,753,693 , GRCh37.p13 chr1: 153,611,393-153,726,169 SNAPIN, NPR1, 7 more genes
    nsv6323294copy number variation1nstd223human GRCh38 chr1: 153,657,740-153,660,981 , GRCh37.p13 chr1: 153,630,216-153,633,457 ILF2, SNAPIN
    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
    nsv6297940copy number variation1nstd186human GRCh37 chr1: 153,608,608-153,640,979 , GRCh38.p12 chr1: 153,636,132-153,668,503 ILF2, SNAPIN, 1 more genes
    nsv6133926copy number variation1nstd213human GRCh37 chr1: 153,540,000-154,010,001 , GRCh38.p12 chr1: 153,567,524-154,037,525 SNAPIN, LOC645965, 26 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
    nsv6133499copy number variation1nstd213human GRCh37 chr1: 149,880,000-153,720,001 , GRCh38.p12 chr1: 149,908,448-153,747,525 , CTSK, 198 more genes
    nsv5422116copy number variation1nstd206human GRCh38 chr1: 153,636,132-153,668,503 , GRCh37.p13 chr1: 153,608,608-153,640,979 SNAPIN, ILF2, 1 more genes
    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
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