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Items: 1 to 20 of 364

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7050849inversion1nstd229human GRCh38 chr2: 64,548,536-64,751,728 , GRCh37.p13 chr2: 64,775,670-64,978,862 SERTAD2, LOC105374775, 5 more genes
    nsv7044394inversion1nstd229human GRCh38 chr2: 64,530,120-64,530,168 , GRCh37.p13 chr2: 64,757,254-64,757,302 AFTPH, LOC105374773
    nsv6675683copy number variation1nstd229human GRCh38 chr2: 64,556,142-64,559,820 , GRCh37.p13 chr2: 64,783,276-64,786,954 LOC105374773, AFTPH
    nsv6674102copy number variation1nstd229human GRCh38 chr2: 64,532,201-64,536,100 , GRCh37.p13 chr2: 64,759,335-64,763,234 AFTPH, LOC105374773
    nsv6671211copy number variation1nstd229human GRCh38 chr2: 64,559,764-64,560,167 , GRCh37.p13 chr2: 64,786,898-64,787,301 LOC105374773, AFTPH
    nsv6668820copy number variation1nstd229human GRCh38 chr2: 64,576,444-64,593,095 , GRCh37.p13 chr2: 64,803,578-64,820,229 RNU6-100P, LOC105374773, 1 more genes
    nsv6666012copy number variation1nstd229human GRCh38 chr2: 64,578,294-64,578,398 , GRCh37.p13 chr2: 64,805,428-64,805,532 RNU6-100P, AFTPH, 1 more genes
    nsv6661768copy number variation1nstd229human GRCh38 chr2: 64,576,092-64,576,119 , GRCh37.p13 chr2: 64,803,226-64,803,253 AFTPH, LOC105374773
    nsv6661490copy number variation1nstd229human GRCh38 chr2: 64,210,609-64,960,847 , GRCh37.p13 chr2: 64,437,743-65,187,981 RN7SL211P, RNU6-100P, 23 more genes
    nsv6660286copy number variation1nstd229human GRCh38 chr2: 64,570,586-64,601,228 , GRCh37.p13 chr2: 64,797,720-64,828,362 LOC105374773, RNU6-100P, 1 more genes
    nsv6658857copy number variation1nstd229human GRCh38 chr2: 64,577,528-64,577,635 , GRCh37.p13 chr2: 64,804,662-64,804,769 RNU6-100P, LOC105374773, 1 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6553652inversion1nstd223human GRCh38 chr2: 64,545,915-64,546,871 , GRCh37.p13 chr2: 64,773,049-64,774,005 LOC105374773, AFTPH
    nsv6551094inversion1nstd223human GRCh38 chr2: 64,078,330-67,334,177 , GRCh37.p13 chr2: 64,305,464-67,561,309 LINC01805, LINC02579, 59 more genes
    nsv6548076inversion1nstd223human GRCh38 chr2: 64,564,633-64,564,912 , GRCh37.p13 chr2: 64,791,767-64,792,046 AFTPH, LOC105374773
    nsv6546897inversion1nstd223human GRCh38 chr2: 64,565,052-64,565,434 , GRCh37.p13 chr2: 64,792,186-64,792,568 LOC105374773, AFTPH
    nsv6537624inversion1nstd223human GRCh38 chr2: 64,575,362-64,575,613 , GRCh37.p13 chr2: 64,802,496-64,802,747 AFTPH, LOC105374773
    nsv6537459inversion1nstd223human GRCh38 chr2: 64,546,133-64,546,764 , GRCh37.p13 chr2: 64,773,267-64,773,898 LOC105374773, AFTPH
    nsv6536483inversion1nstd223human GRCh38 chr2: 64,559,885-64,560,700 , GRCh37.p13 chr2: 64,787,019-64,787,834 AFTPH, LOC105374773
    nsv6354258copy number variation1nstd223human GRCh38 chr2: 64,588,901-64,590,300 , GRCh37.p13 chr2: 64,816,035-64,817,434 AFTPH
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