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Items: 1 to 20 of 129

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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
    nsv7069223inversion1nstd229human GRCh38 chr14: 95,460,643-95,624,077 , GRCh37.p13 chr14: 95,926,980-96,090,414 GLRX5, SNHG10, 5 more genes
    nsv6976685copy number variation1nstd229human GRCh38 chr14: 95,526,267-95,631,591 , GRCh37.p13 chr14: 95,992,604-96,097,928 GLRX5, LOC105370643, 3 more genes
    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
    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
    nsv6505289copy number variation1nstd223human GRCh38 chr14: 95,320,061-95,667,130 , GRCh37.p13 chr14: 95,786,398-96,133,467 SNHG10, LOC105370637, 13 more genes
    nsv6499011copy number variation1nstd223human GRCh38 chr14: 95,580,265-95,582,260 , GRCh37.p13 chr14: 96,046,602-96,048,597 LINC02318
    nsv6315524copy number variation1nstd102humanPathogenic GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013 PAPOLA-DT, LOC105378180, 1338 more genes
    nsv6314100copy number variation1nstd102humanUncertain significance GRCh37 chr14: 94,400,492-96,192,218 , GRCh38.p12 chr14: 94,115,593-95,725,881 DICER1, LOC105370634, 45 more genes
    nsv6291768copy number variation1nstd102humanPathogenic GRCh37 chr14: 95,871,795-102,457,523 , GRCh38.p12 chr14: 95,405,458-101,991,186 CCDC85C, MEG3, 206 more genes
    nsv6132941copy number variation1nstd213human GRCh37 chr14: 95,410,000-96,460,001 , GRCh38.p12 chr14: 94,943,663-95,993,664 DICER1-AS1, TUNAR, 23 more genes
    nsv5863975copy number variation1nstd209human GRCh38 chr14: 95,570,638-95,573,989 , GRCh37.p13 chr14: 96,036,975-96,040,326 LINC02318
    nsv5700306mobile element insertion1nstd211human GRCh38 chr14: 95,582,397-95,582,397 , GRCh37.p13 chr14: 96,048,734-96,048,734 LINC02318
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv5494526copy number variation1nstd206human GRCh38 chr14: 95,579,129-95,579,694 , GRCh37.p13 chr14: 96,045,466-96,046,031 LINC02318
    nsv5424770mobile element insertion1nstd206human GRCh38 chr14: 95,582,397-95,582,448 , GRCh37.p13 chr14: 96,048,734-96,048,785 LINC02318
    nsv5141193mobile element insertion1nstd203human GRCh38 chr14: 95,582,384-95,582,397 , GRCh37.p13 chr14: 96,048,721-96,048,734 LINC02318
    nsv4679492copy number variation1nstd189human GRCh37.p13 chr14: 95,797,225-96,122,325 , GRCh38.p12 chr14: 95,330,888-95,655,988 , TCL6, 12 more genes
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