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Items: 1 to 20 of 140

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7056666inversion1nstd229human GRCh38 chr1: 151,403,323-155,722,147 , GRCh37.p13 chr1: 151,375,799-155,691,938 ILF2, SPRR2C, 219 more genes
    nsv7051862inversion1nstd229human GRCh38 chr1: 152,471,803-152,747,402 , GRCh37.p13 chr1: 152,444,279-152,719,878 CRCT1, LCE5A, 16 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
    nsv6537547inversion1nstd223human GRCh38 chr1: 152,461,479-152,881,493 , GRCh37.p13 chr1: 152,433,955-152,853,969 LCEP2, LOC105371445, 27 more genes
    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
    nsv6290434copy number variation1nstd102humanLikely benign GRCh37 chr1: 152,461,314-152,519,237 , GRCh38.p12 chr1: 152,488,838-152,546,761 CRCT1, LCE5A
    nsv6133924copy number variation1nstd213human GRCh37 chr1: 152,390,000-152,520,001 , GRCh38.p12 chr1: 152,417,524-152,547,525 CRCT1, LCE5A
    nsv6133734copy number variation1nstd213human GRCh37 chr1: 150,350,000-154,440,001 , GRCh38.p12 chr1: 150,377,524-154,467,525 , MCL1, 216 more genes
    nsv6133732copy number variation1nstd213human GRCh37 chr1: 149,750,000-153,310,001 , GRCh38.p12 chr1: 149,778,444-153,337,525 , CTSK, 183 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
    nsv5421580copy number variation1nstd206human GRCh38 chr1: 152,489,543-152,734,782 , GRCh37.p13 chr1: 152,462,019-152,707,258 LCE2D, LCE5A, 14 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
    nsv4781194copy number variation1nstd200human GRCh37 chr1: 152,461,990-152,707,312 , GRCh38.p12 chr1: 152,489,514-152,734,836 LCE2B, LCEP3, 14 more genes
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4712913copy number variation1nstd195human GRCh37 chr1: 152,464,001-152,520,451 , GRCh38.p12 chr1: 152,491,525-152,547,975 CRCT1, LCE5A
    nsv4579206copy number variation1nstd183human GRCh37 chr1: 152,464,856-152,519,209 , GRCh38.p12 chr1: 152,492,380-152,546,733 LCE5A, CRCT1
    nsv4579205copy number variation1nstd183human GRCh37 chr1: 152,464,303-152,519,252 , GRCh38.p12 chr1: 152,491,827-152,546,776 LCE5A, CRCT1
    nsv4385653copy number variation1nstd173human GRCh37 chr1: 152,446,839-152,659,909 , GRCh38.p12 chr1: 152,474,363-152,687,433 LCE2B, LCEP3, 11 more genes
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