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Items: 1 to 20 of 128

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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
    nsv6642064copy number variation1nstd229human GRCh38 chr1: 152,843,204-152,843,366 , GRCh37.p13 chr1: 152,815,680-152,815,842 LCE6A
    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
    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
    nsv6133736copy number variation1nstd213human GRCh37 chr1: 152,780,000-153,030,001 , GRCh38.p12 chr1: 152,807,524-153,057,525 IVL, SPRR1A, 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
    nsv5676746mobile element insertion2nstd211human GRCh38 chr1: 152,841,087-152,841,087 , GRCh37.p13 chr1: 152,813,563-152,813,563 LCE6A
    nsv5422361copy number variation1nstd206human GRCh38 chr1: 152,832,587-152,881,000 , GRCh37.p13 chr1: 152,805,063-152,853,476 LCE6A, LOC105371444, 2 more genes
    nsv5406211mobile element insertion1nstd206human GRCh38 chr1: 152,841,087-152,841,138 , GRCh37.p13 chr1: 152,813,563-152,813,614 LCE6A
    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
    nsv5213223copy number variation1nstd204human GRCh38.p13 chr1: 152,831,103-152,872,395 , GRCh37.p13 chr1: 152,803,579-152,844,871 LCE6A, LOC105371445, 1 more genes
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