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Items: 1 to 20 of 160

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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
    nsv6642078copy number variation1nstd229human GRCh38 chr1: 153,125,837-153,509,102 , GRCh37.p13 chr1: 153,098,313-153,481,578 PGLYRP4, S100A7, 19 more genes
    nsv6642077copy number variation1nstd229human GRCh38 chr1: 153,122,301-153,253,000 , GRCh37.p13 chr1: 153,094,777-153,225,476 LOC101928009, SPRR2C, 4 more genes
    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
    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
    nsv6334542copy number variation1nstd223human GRCh38 chr1: 153,190,788-153,191,341 , GRCh37.p13 chr1: 153,163,264-153,163,817 LOC101928009, SPRR2G
    nsv6329719copy number variation1nstd223human GRCh38 chr1: 153,190,225-153,190,643 , GRCh37.p13 chr1: 153,162,701-153,163,119 LOC101928009, SPRR2G
    nsv6315665copy number variation1nstd223human GRCh38 chr1: 153,174,396-153,184,756 , GRCh37.p13 chr1: 153,146,872-153,157,232 LOC101928009, SPRR2G
    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
    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
    nsv6133501copy number variation1nstd213human GRCh37 chr1: 153,030,000-153,260,001 , GRCh38.p12 chr1: 153,057,524-153,287,525 SPRR2F, LOC101928009, 9 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
    nsv5423696copy number variation1nstd206human GRCh38 chr1: 153,176,616-153,176,703 , GRCh37.p13 chr1: 153,149,092-153,149,179 SPRR2G, LOC101928009
    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
    nsv5164556mobile element insertion1nstd203human GRCh38 chr1: 153,178,145-153,178,161 , GRCh37.p13 chr1: 153,150,621-153,150,637 SPRR2G, LOC101928009
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