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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137135copy number variation1nstd102humanPathogenic GRCh37 chr14: 88,401,076-94,725,706 , GRCh38.p12 chr14: 87,934,732-94,140,555 LOC100128939, FAM181A-AS1, 104 more genes
    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
    nsv7094350copy number variation1nstd102humanUncertain significance GRCh37 chr14: 90,429,459-94,856,914 , GRCh38.p12 chr14: 89,963,115-94,390,577 LOC105370619, SLC24A4, 78 more genes
    nsv7074693inversion1nstd229human GRCh38 chr14: 90,587,174-90,587,378 , GRCh37.p13 chr14: 91,053,518-91,053,722 TTC7B
    nsv7059378inversion1nstd229human GRCh38 chr14: 87,626,566-93,230,083 , GRCh37.p13 chr14: 88,092,910-93,674,575 PSMC1, HISLA, 87 more genes
    nsv7058992inversion1nstd229human GRCh38 chr14: 90,104,468-93,174,563 , GRCh37.p13 chr14: 90,570,812-93,372,264 LINC02321, TC2N, 48 more genes
    nsv6977680copy number variation1nstd229human GRCh38 chr14: 90,687,833-90,688,483 , GRCh37.p13 chr14: 91,154,177-91,154,827 TTC7B
    nsv6977315copy number variation1nstd229human GRCh38 chr14: 90,552,023-90,552,761 , GRCh37.p13 chr14: 91,018,367-91,019,105 TTC7B
    nsv6975799copy number variation1nstd229human GRCh38 chr14: 90,805,828-90,805,858 , GRCh37.p13 chr14: 91,272,172-91,272,202 TTC7B
    nsv6975547copy number variation1nstd229human GRCh38 chr14: 90,553,039-90,569,283 , GRCh37.p13 chr14: 91,019,383-91,035,627 TTC7B
    nsv6975411copy number variation1nstd229human GRCh38 chr14: 90,789,901-90,803,200 , GRCh37.p13 chr14: 91,256,245-91,269,544 TTC7B
    nsv6975239copy number variation1nstd229human GRCh38 chr14: 90,680,483-90,685,824 , GRCh37.p13 chr14: 91,146,827-91,152,168 TTC7B
    nsv6974881copy number variation1nstd229human GRCh38 chr14: 90,622,794-90,627,101 , GRCh37.p13 chr14: 91,089,138-91,093,445 TTC7B
    nsv6974616copy number variation1nstd229human GRCh38 chr14: 90,788,001-90,800,700 , GRCh37.p13 chr14: 91,254,345-91,267,044 TTC7B
    nsv6973331copy number variation1nstd229human GRCh38 chr14: 90,789,887-90,801,216 , GRCh37.p13 chr14: 91,256,231-91,267,560 TTC7B
    nsv6972831copy number variation1nstd229human GRCh38 chr14: 90,622,382-90,625,113 , GRCh37.p13 chr14: 91,088,726-91,091,457 TTC7B
    nsv6972020copy number variation1nstd229human GRCh38 chr14: 90,596,728-90,600,369 , GRCh37.p13 chr14: 91,063,072-91,066,713 TTC7B
    nsv6971764copy number variation1nstd229human GRCh38 chr14: 90,727,985-90,728,090 , GRCh37.p13 chr14: 91,194,329-91,194,434 TTC7B
    nsv6970757copy number variation1nstd229human GRCh38 chr14: 90,701,251-90,710,676 , GRCh37.p13 chr14: 91,167,595-91,177,020 TTC7B
    nsv6970358copy number variation1nstd229human GRCh38 chr14: 90,664,816-90,667,485 , GRCh37.p13 chr14: 91,131,160-91,133,829 TTC7B
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