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Items: 1 to 20 of 368

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099233copy number variation1nstd231human GRCh38.p12 chr1: 152,557,316-153,481,153 , GRCh37 chr1: 152,529,792-153,453,629 IVL, LORICRIN, 57 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
    nsv6642164copy number variation1nstd229human GRCh38 chr1: 152,572,695-153,147,548 , GRCh37.p13 chr1: 152,545,171-153,120,024 LINC01527, LCE1C, 37 more genes
    nsv6642059copy number variation1nstd229human GRCh38 chr1: 152,787,401-152,796,600 , GRCh37.p13 chr1: 152,759,877-152,769,076 LCE1D, LCE1E
    nsv6641952copy number variation1nstd229human GRCh38 chr1: 152,675,695-153,317,474 , GRCh37.p13 chr1: 152,648,171-153,289,950 LCE1E, SPRR2E, 36 more genes
    nsv6641950copy number variation1nstd229human GRCh38 chr1: 152,583,101-152,798,600 , GRCh37.p13 chr1: 152,555,577-152,771,076 LCE3C, LINC00302, 16 more genes
    nsv6636415copy number variation1nstd102humanUncertain significance GRCh37 chr1: 152,648,864-153,286,218 , GRCh38.p12 chr1: 152,676,388-153,313,742 KPRP, LCE1A, 36 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
    nsv6333251copy number variation1nstd223human GRCh38 chr1: 152,726,601-152,836,400 , GRCh37.p13 chr1: 152,699,077-152,808,876 LCE1C, LCE1B, 7 more genes
    nsv6322103copy number variation1nstd223human GRCh38 chr1: 152,787,001-152,798,300 , GRCh37.p13 chr1: 152,759,477-152,770,776 LCE1E, LCE1D
    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
    nsv6133925copy number variation1nstd213human GRCh37 chr1: 152,620,000-152,780,001 , GRCh38.p12 chr1: 152,647,524-152,807,525 LCE1D, LCE1F, 13 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
    nsv6133732copy number variation1nstd213human GRCh37 chr1: 149,750,000-153,310,001 , GRCh38.p12 chr1: 149,778,444-153,337,525 , CTSK, 183 more genes
    nsv6133557copy number variation1nstd213human GRCh37 chr1: 152,640,000-153,440,001 , GRCh38.p12 chr1: 152,667,524-153,467,525 LORICRIN, IVL, 48 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
    nsv5981517copy number variation1nstd212human GRCh38 chr1: 152,788,295-152,796,565 , GRCh37.p13 chr1: 152,760,771-152,769,041 LCE1E, LCE1D
    nsv5877731copy number variation1nstd209human GRCh38 chr1: 152,788,113-152,798,550 , GRCh37.p13 chr1: 152,760,589-152,771,026 LCE1E, LCE1D
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