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Items: 1 to 20 of 171

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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
    nsv7057327inversion1nstd229human GRCh38 chr1: 153,068,245-153,079,052 , GRCh37.p13 chr1: 153,040,721-153,051,528 SPRR2B
    nsv7056666inversion1nstd229human GRCh38 chr1: 151,403,323-155,722,147 , GRCh37.p13 chr1: 151,375,799-155,691,938 ILF2, SPRR2C, 219 more genes
    nsv7054443inversion1nstd229human GRCh38 chr1: 153,032,790-153,133,643 , GRCh37.p13 chr1: 153,005,266-153,106,119 SPRR1B, SPRR2F, 4 more genes
    nsv7049201inversion1nstd229human GRCh38 chr1: 153,038,172-153,130,109 , GRCh37.p13 chr1: 153,010,648-153,102,585 SPRR2A, SPRR2D, 3 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
    nsv6642404copy number variation1nstd229human GRCh38 chr1: 153,070,201-153,096,700 , GRCh37.p13 chr1: 153,042,677-153,069,176 SPRR2B, SPRR2E
    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
    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
    nsv6324938copy number variation1nstd223human GRCh38 chr1: 153,070,701-153,071,300 , GRCh37.p13 chr1: 153,043,177-153,043,776 SPRR2B
    nsv6317579copy number variation1nstd223human GRCh38 chr1: 153,056,279-153,070,312 , GRCh37.p13 chr1: 153,028,755-153,042,788 SPRR2A, SPRR2B
    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
    nsv5558254sequence alteration1nstd206human GRCh38 chr1: 153,068,245-153,079,145 , GRCh37.p13 chr1: 153,040,721-153,051,621 SPRR2B
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