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Items: 1 to 20 of 156

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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
    nsv7058129inversion1nstd229human GRCh38 chr14: 95,664,622-95,664,635 , GRCh37.p13 chr14: 96,130,959-96,130,972 TCL6
    nsv6973262copy number variation1nstd229human GRCh38 chr14: 95,640,070-95,656,387 , GRCh37.p13 chr14: 96,106,407-96,122,724 TCL6
    nsv6970720copy number variation1nstd229human GRCh38 chr14: 95,656,232-95,659,277 , GRCh37.p13 chr14: 96,122,569-96,125,614 TCL6
    nsv6965420copy number variation1nstd229human GRCh38 chr14: 95,653,859-95,671,220 , GRCh37.p13 chr14: 96,120,196-96,137,557 TCL6
    nsv6964585copy number variation1nstd229human GRCh38 chr14: 95,668,040-95,678,464 , GRCh37.p13 chr14: 96,134,377-96,144,801 TCL6
    nsv6963938copy number variation1nstd229human GRCh38 chr14: 95,660,085-95,678,335 , GRCh37.p13 chr14: 96,126,422-96,144,672 TCL6
    nsv6962847copy number variation1nstd229human GRCh38 chr14: 95,646,378-95,666,012 , GRCh37.p13 chr14: 96,112,715-96,132,349 TCL6
    nsv6959282copy number variation1nstd229human GRCh38 chr14: 95,668,301-95,674,569 , GRCh37.p13 chr14: 96,134,638-96,140,906 TCL6
    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
    nsv6622698copy number variation4nstd224human GRCh37 chr14: 96,127,082-96,141,240 , GRCh38.p12 chr14: 95,660,745-95,674,903 TCL6
    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
    nsv6508153copy number variation1nstd223human GRCh38 chr14: 95,646,387-95,665,977 , GRCh37.p13 chr14: 96,112,724-96,132,314 TCL6
    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
    nsv6503997copy number variation1nstd223human GRCh38 chr14: 95,660,084-95,678,334 , GRCh37.p13 chr14: 96,126,421-96,144,671 TCL6
    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
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