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Items: 1 to 20 of 219

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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
    nsv7054580inversion1nstd229human GRCh38 chr1: 33,076,956-33,688,708 , GRCh37.p13 chr1: 33,542,557-34,154,308 RN7SKP16, ZNF362, 11 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
    nsv6649149copy number variation1nstd229human GRCh38 chr1: 33,147,955-33,150,864 , GRCh37.p13 chr1: 33,613,556-33,616,465 AZIN2, TRIM62
    nsv6649148copy number variation1nstd229human GRCh38 chr1: 33,099,994-33,100,020 , GRCh37.p13 chr1: 33,565,595-33,565,621 AZIN2
    nsv6649001copy number variation1nstd229human GRCh38 chr1: 33,098,201-33,103,800 , GRCh37.p13 chr1: 33,563,802-33,569,401 AZIN2
    nsv6648957copy number variation1nstd229human GRCh38 chr1: 33,152,466-33,154,698 , GRCh37.p13 chr1: 33,618,067-33,620,299 TRIM62, AZIN2
    nsv6648956copy number variation1nstd229human GRCh38 chr1: 33,120,087-33,128,408 , GRCh37.p13 chr1: 33,585,688-33,594,009 AZIN2
    nsv6648955copy number variation1nstd229human GRCh38 chr1: 33,113,201-33,115,800 , GRCh37.p13 chr1: 33,578,802-33,581,401 AZIN2
    nsv6648954copy number variation1nstd229human GRCh38 chr1: 33,100,430-33,103,891 , GRCh37.p13 chr1: 33,566,031-33,569,492 AZIN2
    nsv6648952copy number variation1nstd229human GRCh38 chr1: 33,094,722-33,094,930 , GRCh37.p13 chr1: 33,560,323-33,560,531 AZIN2
    nsv6648922copy number variation1nstd229human GRCh38 chr1: 33,090,556-33,100,063 , GRCh37.p13 chr1: 33,556,157-33,565,664 AZIN2
    nsv6648920copy number variation1nstd229human GRCh38 chr1: 33,034,541-33,209,380 , GRCh37.p13 chr1: 33,500,142-33,674,981 TRIM62, AZIN2, 2 more genes
    nsv6648919copy number variation1nstd229human GRCh38 chr1: 33,016,111-33,117,277 , GRCh37.p13 chr1: 33,481,712-33,582,878 LOC105378635, AK2, 1 more genes
    nsv6648499copy number variation1nstd229human GRCh38 chr1: 33,150,323-33,150,651 , GRCh37.p13 chr1: 33,615,924-33,616,252 AZIN2, TRIM62
    nsv6648497copy number variation1nstd229human GRCh38 chr1: 33,087,384-33,099,040 , GRCh37.p13 chr1: 33,552,985-33,564,641 AZIN2
    nsv6553937inversion1nstd223human GRCh38 chr1: 33,114,805-33,115,415 , GRCh37.p13 chr1: 33,580,406-33,581,016 AZIN2
    nsv6548474inversion1nstd223human GRCh38 chr1: 33,100,334-33,100,867 , GRCh37.p13 chr1: 33,565,935-33,566,468 AZIN2
    nsv6321079copy number variation1nstd223human GRCh38 chr1: 33,090,601-33,100,000 , GRCh37.p13 chr1: 33,556,202-33,565,601 AZIN2
    nsv6313688copy number variation1nstd102humanPathogenic GRCh37 chr1: 33,285,582-47,891,811 , GRCh38.p12 chr1: 32,819,981-47,426,139 LOC107984940, PPIAP36, 407 more genes
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