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Items: 1 to 20 of 205

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099193copy number variation1nstd231human GRCh38.p12 chr1: 32,456,017-38,905,781 , GRCh37 chr1: 32,921,618-39,371,453 AK2, COL8A2, 151 more genes
    nsv7046918inversion1nstd229human GRCh38 chr1: 34,689,928-38,980,899 , GRCh37.p13 chr1: 35,155,529-39,446,571 LOC105378647, NCDN, 112 more genes
    nsv7046389inversion1nstd229human GRCh38 chr1: 31,492,639-36,569,102 , GRCh37.p13 chr1: 32,017,064-37,034,703 LOC105378642, TMEM35B, 127 more genes
    nsv7040332inversion1nstd229human GRCh38 chr1: 34,936,903-38,057,517 , GRCh37.p13 chr1: 35,402,504-38,523,189 MAP7D1, RPL12P45, 83 more genes
    nsv6649459copy number variation1nstd229human GRCh38 chr1: 35,873,807-35,878,344 , GRCh37.p13 chr1: 36,339,408-36,343,945 AGO1
    nsv6649458copy number variation1nstd229human GRCh38 chr1: 35,861,601-35,874,000 , GRCh37.p13 chr1: 36,327,202-36,339,601 AGO1
    nsv6649283copy number variation1nstd229human GRCh38 chr1: 35,926,801-35,926,941 , GRCh37.p13 chr1: 36,392,402-36,392,542 AGO1, AGO3
    nsv6649282copy number variation1nstd229human GRCh38 chr1: 35,897,973-35,897,997 , GRCh37.p13 chr1: 36,363,574-36,363,598 AGO1
    nsv6649281copy number variation1nstd229human GRCh38 chr1: 35,865,879-35,871,311 , GRCh37.p13 chr1: 36,331,480-36,336,912 AGO1
    nsv6649280copy number variation1nstd229human GRCh38 chr1: 35,864,710-35,868,419 , GRCh37.p13 chr1: 36,330,311-36,334,020 AGO1
    nsv6648787copy number variation1nstd229human GRCh38 chr1: 35,688,883-35,912,121 , GRCh37.p13 chr1: 36,154,484-36,377,722 CLSPN, AGO1, 2 more genes
    nsv6636592copy number variation1nstd102humanPathogenic GRCh37 chr1: 35,104,233-37,357,913 , GRCh38.p12 chr1: 34,638,632-36,892,312 EFCAB14P1, SNORA63C, 56 more genes
    nsv6554664inversion1nstd223human GRCh38 chr1: 35,903,909-35,904,148 , GRCh37.p13 chr1: 36,369,510-36,369,749 AGO1
    nsv6546798inversion1nstd223human GRCh38 chr1: 35,912,077-35,912,567 , GRCh37.p13 chr1: 36,377,678-36,378,168 AGO1
    nsv6541890inversion1nstd223human GRCh38 chr1: 35,871,950-35,872,196 , GRCh37.p13 chr1: 36,337,551-36,337,797 AGO1
    nsv6334685copy number variation1nstd223human GRCh38 chr1: 35,927,701-35,933,800 , GRCh37.p13 chr1: 36,393,302-36,399,401 AGO3, AGO1
    nsv6331004copy number variation1nstd223human GRCh38 chr1: 35,869,493-35,870,501 , GRCh37.p13 chr1: 36,335,094-36,336,102 AGO1
    nsv6330114copy number variation1nstd223human GRCh38 chr1: 35,881,805-35,882,199 , GRCh37.p13 chr1: 36,347,406-36,347,800 AGO1
    nsv6329078copy number variation1nstd223human GRCh38 chr1: 35,861,610-35,874,028 , GRCh37.p13 chr1: 36,327,211-36,339,629 AGO1
    nsv6313765copy number variation1nstd102humanUncertain significance GRCh37 chr1: 36,041,366-39,112,237 , GRCh38.p12 chr1: 35,575,765-38,646,565 RNU6-510P, AGO3, 78 more genes
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