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Items: 1 to 20 of 559

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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
    nsv7075568inversion1nstd229human GRCh38 chr14: 92,512,257-92,512,348 , GRCh37.p13 chr14: 92,978,601-92,978,692 RIN3
    nsv7069800inversion1nstd229human GRCh38 chr14: 92,544,892-92,650,462 , GRCh37.p13 chr14: 93,011,237-93,116,807 RIN3
    nsv7059553inversion1nstd229human GRCh38 chr14: 92,340,771-92,517,428 , GRCh37.p13 chr14: 92,807,115-92,983,772 RIN3, SLC24A4
    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
    nsv7058760inversion1nstd229human GRCh38 chr14: 92,604,806-92,607,635 , GRCh37.p13 chr14: 93,071,151-93,073,980 RIN3
    nsv6977152copy number variation1nstd229human GRCh38 chr14: 92,636,101-92,638,800 , GRCh37.p13 chr14: 93,102,446-93,105,145 RIN3
    nsv6975696copy number variation1nstd229human GRCh38 chr14: 92,666,035-92,666,072 , GRCh37.p13 chr14: 93,132,380-93,132,417 RIN3
    nsv6974443copy number variation1nstd229human GRCh38 chr14: 92,689,488-92,700,104 , GRCh37.p13 chr14: 93,155,833-93,166,449 RIN3
    nsv6971540copy number variation1nstd229human GRCh38 chr14: 92,556,233-92,559,582 , GRCh37.p13 chr14: 93,022,578-93,025,927 RIN3
    nsv6970113copy number variation1nstd229human GRCh38 chr14: 92,542,919-92,551,356 , GRCh37.p13 chr14: 93,009,264-93,017,701 RIN3
    nsv6969717copy number variation1nstd229human GRCh38 chr14: 92,563,113-92,576,769 , GRCh37.p13 chr14: 93,029,458-93,043,114 RIN3
    nsv6966536copy number variation1nstd229human GRCh38 chr14: 92,523,801-92,537,800 , GRCh37.p13 chr14: 92,990,145-93,004,144 RIN3
    nsv6965395copy number variation1nstd229human GRCh38 chr14: 92,605,340-92,607,868 , GRCh37.p13 chr14: 93,071,685-93,074,213 RIN3
    nsv6962700copy number variation1nstd229human GRCh38 chr14: 92,572,127-92,572,275 , GRCh37.p13 chr14: 93,038,472-93,038,620 RIN3
    nsv6962339copy number variation1nstd229human GRCh38 chr14: 92,514,893-92,519,320 , GRCh37.p13 chr14: 92,981,237-92,985,664 RIN3
    nsv6962332copy number variation1nstd229human GRCh38 chr14: 92,555,320-92,559,264 , GRCh37.p13 chr14: 93,021,665-93,025,609 RIN3
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