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Items: 1 to 20 of 204

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057873inversion1nstd229human GRCh38 chr7: 29,679,024-30,286,151 , GRCh37.p13 chr7: 29,718,640-30,325,767 SCRN1, LOC105375217, 13 more genes
    nsv7040921inversion1nstd229human GRCh38 chr7: 29,656,957-32,757,617 , GRCh37.p13 chr7: 29,696,573-32,797,229 LSM5, RPS27P16, 51 more genes
    nsv6837929copy number variation1nstd229human GRCh38 chr7: 29,961,752-29,961,805 , GRCh37.p13 chr7: 30,001,368-30,001,421 SCRN1
    nsv6837342copy number variation1nstd229human GRCh38 chr7: 29,919,704-29,919,899 , GRCh37.p13 chr7: 29,959,320-29,959,515 SCRN1
    nsv6835730copy number variation1nstd229human GRCh38 chr7: 29,985,401-30,392,500 , GRCh37.p13 chr7: 30,025,017-30,432,116 PLEKHA8, FKBP14, 12 more genes
    nsv6828251copy number variation1nstd229human GRCh38 chr7: 29,923,501-29,926,200 , GRCh37.p13 chr7: 29,963,117-29,965,816 SCRN1
    nsv6828127copy number variation1nstd229human GRCh38 chr7: 29,982,401-29,988,700 , GRCh37.p13 chr7: 30,022,017-30,028,316 SCRN1, FKBP14-AS1
    nsv6824272copy number variation1nstd229human GRCh38 chr7: 29,929,577-29,935,542 , GRCh37.p13 chr7: 29,969,193-29,975,158 SCRN1
    nsv6823162copy number variation1nstd229human GRCh38 chr7: 29,917,905-29,918,225 , GRCh37.p13 chr7: 29,957,521-29,957,841 SCRN1
    nsv6636445copy number variation1nstd102humanPathogenic GRCh37 chr7: 27,133,786-34,466,477 , GRCh38.p12 chr7: 27,094,167-34,426,865 MIR550A1, HOXA-AS3, 119 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6605338copy number variation1nstd223human GRCh38 chr7: 29,984,815-29,985,326 , GRCh37.p13 chr7: 30,024,431-30,024,942 SCRN1
    nsv6571632inversion1nstd223human GRCh38 chr7: 29,932,657-29,932,838 , GRCh37.p13 chr7: 29,972,273-29,972,454 SCRN1
    nsv6564403inversion1nstd223human GRCh38 chr7: 29,963,174-29,969,549 , GRCh37.p13 chr7: 30,002,790-30,009,165 SCRN1
    nsv6556278inversion1nstd223human GRCh38 chr7: 29,684,558-32,729,318 , GRCh37.p13 chr7: 29,724,174-32,768,930 LOC105375219, CRHR2, 47 more genes
    nsv6315453copy number variation1nstd102humanPathogenic GRCh37 chr7: 25,451,740-33,864,069 , GRCh38.p12 chr7: 25,412,121-33,824,457 PLEKHA8, NFE2L3, 141 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313670copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 27,507,832-39,072,473 , GRCh38.p12 chr7: 27,468,213-39,032,873 ADCYAP1R1, AMPH, 175 more genes
    nsv6313493copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 10,745,750-35,305,167 , GRCh38.p12 chr7: 10,706,123-35,265,556 ADCYAP1R1, AHR, 329 more genes
    nsv6261236mobile element insertion1nstd215human GRCh38 chr7: 29,941,131-29,941,131 , GRCh37.p13 chr7: 29,980,747-29,980,747 SCRN1
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