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Items: 1 to 20 of 212

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7066609inversion1nstd229human GRCh38 chr14: 81,185,002-81,191,926 , GRCh37.p13 chr14: 81,651,346-81,658,270 GTF2A1
    nsv7066414inversion1nstd229human GRCh38 chr14: 79,890,342-89,436,638 , GRCh37.p13 chr14: 80,356,685-89,902,982 SPATA7, RNU6ATAC28P, 82 more genes
    nsv7060344inversion1nstd229human GRCh38 chr14: 81,104,679-81,358,991 , GRCh37.p13 chr14: 81,571,023-81,825,335 STON2, LOC105370594, 8 more genes
    nsv6976754copy number variation1nstd229human GRCh38 chr14: 81,182,762-81,183,263 , GRCh37.p13 chr14: 81,649,106-81,649,607 GTF2A1
    nsv6976254copy number variation1nstd229human GRCh38 chr14: 81,187,401-81,187,971 , GRCh37.p13 chr14: 81,653,745-81,654,315 GTF2A1
    nsv6971662copy number variation1nstd229human GRCh38 chr14: 81,205,301-81,208,634 , GRCh37.p13 chr14: 81,671,645-81,674,978 GTF2A1
    nsv6967066copy number variation1nstd229human GRCh38 chr14: 81,207,629-81,212,286 , GRCh37.p13 chr14: 81,673,973-81,678,630 GTF2A1
    nsv6964424copy number variation1nstd229human GRCh38 chr14: 81,210,023-81,210,053 , GRCh37.p13 chr14: 81,676,367-81,676,397 GTF2A1
    nsv6963417copy number variation1nstd229human GRCh38 chr14: 81,184,411-81,206,369 , GRCh37.p13 chr14: 81,650,755-81,672,713 SNORA79, GTF2A1
    nsv6959895copy number variation1nstd229human GRCh38 chr14: 76,053,610-84,350,797 , GRCh37.p13 chr14: 76,519,953-84,817,141 LINC02308, LOC105370573, 102 more genes
    nsv6637462copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 81,593,708-97,059,276 , GRCh38.p12 chr14: 81,127,364-96,592,939 SERPINA3, BDKRB1, 210 more genes
    nsv6622755copy number variation1nstd224human GRCh37 chr14: 81,150,895-81,838,594 , GRCh38.p12 chr14: 80,684,551-81,372,250 CEP128, UNGP3, 13 more genes
    nsv6582161inversion1nstd223human GRCh38 chr14: 77,269,745-86,636,480 , GRCh37.p13 chr14: 77,736,088-87,102,824 LINC02328, UNGP3, 84 more genes
    nsv6495429copy number variation1nstd223human GRCh38 chr14: 81,190,101-81,192,300 , GRCh37.p13 chr14: 81,656,445-81,658,644 GTF2A1
    nsv6493681copy number variation1nstd223human GRCh38 chr14: 81,187,399-81,187,971 , GRCh37.p13 chr14: 81,653,743-81,654,315 GTF2A1
    nsv6493164copy number variation1nstd223human GRCh38 chr14: 81,182,762-81,183,263 , GRCh37.p13 chr14: 81,649,106-81,649,607 GTF2A1
    nsv6492611copy number variation1nstd223human GRCh38 chr14: 81,178,154-81,178,582 , GRCh37.p13 chr14: 81,644,498-81,644,926 GTF2A1
    nsv6491731copy number variation1nstd223human GRCh38 chr14: 81,219,801-81,220,500 , GRCh37.p13 chr14: 81,686,145-81,686,844 GTF2A1-AS1, GTF2A1
    nsv6488347copy number variation1nstd223human GRCh38 chr14: 81,219,401-81,222,600 , GRCh37.p13 chr14: 81,685,745-81,688,944 GTF2A1, GTF2A1-AS1
    nsv6486501copy number variation1nstd223human GRCh38 chr14: 81,207,629-81,212,283 , GRCh37.p13 chr14: 81,673,973-81,678,627 GTF2A1
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