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Items: 1 to 20 of 136

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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
    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
    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
    nsv6614167copy number variation1nstd223human GRCh38 chr7: 30,018,901-30,021,300 , GRCh37.p13 chr7: 30,058,517-30,060,916 FKBP14, FKBP14-AS1
    nsv6574540inversion1nstd223human GRCh38 chr7: 30,008,723-30,009,523 , GRCh37.p13 chr7: 30,048,339-30,049,139 FKBP14-AS1, FKBP14
    nsv6574320inversion1nstd223human GRCh38 chr7: 30,016,532-30,017,490 , GRCh37.p13 chr7: 30,056,148-30,057,106 FKBP14-AS1, FKBP14
    nsv6557731inversion1nstd223human GRCh38 chr7: 30,015,142-30,015,850 , GRCh37.p13 chr7: 30,054,758-30,055,466 FKBP14, FKBP14-AS1
    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
    nsv6312540copy number variation1nstd102humanUncertain significance GRCh37 chr7: 30,054,351-31,018,859 , GRCh38.p12 chr7: 30,014,735-30,979,244 GARS1-DT, GHRHR, 25 more genes
    nsv6171346copy number variation1nstd214human GRCh38 chr7: 30,011,535-30,011,596 , GRCh37.p13 chr7: 30,051,151-30,051,212 FKBP14-AS1, FKBP14
    nsv6169219copy number variation1nstd214human GRCh38 chr7: 30,011,540-30,011,610 , GRCh37.p13 chr7: 30,051,156-30,051,226 FKBP14, FKBP14-AS1
    nsv6078907insertion1nstd212human GRCh38 chr7: 30,011,577-30,011,577 , GRCh37.p13 chr7: 30,051,193-30,051,193 FKBP14-AS1, FKBP14
    nsv6071393insertion1nstd212human GRCh38 chr7: 30,011,535-30,011,535 , GRCh37.p13 chr7: 30,051,151-30,051,151 FKBP14-AS1, FKBP14
    nsv5922472copy number variation1nstd209human GRCh38 chr7: 30,008,447-30,008,702 , GRCh37.p13 chr7: 30,048,063-30,048,318 FKBP14-AS1, FKBP14
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