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Items: 1 to 20 of 188

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094351copy number variation1nstd102humanUncertain significance GRCh37 chr14: 90,429,459-97,347,545 , GRCh38.p12 chr14: 89,963,115-96,881,208 FBLN5, CYB5AP3, 135 more genes
    nsv7094272copy number variation1nstd102humanUncertain significance GRCh37 chr14: 95,080,779-97,347,545 , GRCh38.p12 chr14: 94,614,442-96,881,208 ADIPOR1P2, LOC105370637, 48 more genes
    nsv7077173inversion1nstd229human GRCh38 chr14: 96,042,489-96,309,879 , GRCh37.p13 chr14: 96,508,826-96,776,216 C14orf132, BDKRB2, 3 more genes
    nsv7065819inversion1nstd229human GRCh38 chr14: 96,052,815-96,153,915 , GRCh37.p13 chr14: 96,519,152-96,620,252 C14orf132
    nsv6977378copy number variation1nstd229human GRCh38 chr14: 96,061,029-96,069,364 , GRCh37.p13 chr14: 96,527,366-96,535,701 C14orf132
    nsv6977256copy number variation1nstd229human GRCh38 chr14: 96,061,101-96,070,900 , GRCh37.p13 chr14: 96,527,438-96,537,237 C14orf132
    nsv6975591copy number variation1nstd229human GRCh38 chr14: 96,071,115-96,116,493 , GRCh37.p13 chr14: 96,537,452-96,582,830 C14orf132
    nsv6974095copy number variation1nstd229human GRCh38 chr14: 96,046,179-96,057,888 , GRCh37.p13 chr14: 96,512,516-96,524,225 C14orf132
    nsv6972360copy number variation1nstd229human GRCh38 chr14: 96,074,615-96,144,489 , GRCh37.p13 chr14: 96,540,952-96,610,826 C14orf132
    nsv6966770copy number variation1nstd229human GRCh38 chr14: 96,061,001-96,070,700 , GRCh37.p13 chr14: 96,527,338-96,537,037 C14orf132
    nsv6962437copy number variation1nstd229human GRCh38 chr14: 96,049,555-96,055,170 , GRCh37.p13 chr14: 96,515,892-96,521,507 C14orf132
    nsv6962314copy number variation1nstd229human GRCh38 chr14: 96,013,696-96,053,685 , GRCh37.p13 chr14: 96,480,033-96,520,022 C14orf132
    nsv6961950copy number variation1nstd229human GRCh38 chr14: 96,056,300-96,070,075 , GRCh37.p13 chr14: 96,522,637-96,536,412 C14orf132
    nsv6961855copy number variation1nstd229human GRCh38 chr14: 96,042,501-96,308,000 , GRCh37.p13 chr14: 96,508,838-96,774,337 BDKRB2, ATG2B, 3 more genes
    nsv6959272copy number variation1nstd229human GRCh38 chr14: 96,081,186-96,083,387 , GRCh37.p13 chr14: 96,547,523-96,549,724 C14orf132
    nsv6958536copy number variation1nstd229human GRCh38 chr14: 96,017,101-96,106,700 , GRCh37.p13 chr14: 96,483,438-96,573,037 C14orf132
    nsv6637825copy number variation1nstd102humanPathogenic GRCh37 chr14: 84,537,502-107,285,437 , GRCh38.p12 chr14: 84,071,158-106,877,229 CHGA, SNORD114-26, 676 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
    nsv6582782inversion1nstd223human GRCh38 chr14: 96,048,038-96,048,635 , GRCh37.p13 chr14: 96,514,375-96,514,972 C14orf132
    nsv6510019copy number variation1nstd223human GRCh38 chr14: 95,535,227-96,112,095 , GRCh37.p13 chr14: 96,001,564-96,578,432 LOC105370643, LINC02318, 9 more genes
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