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Items: 1 to 20 of 449

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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
    nsv7094349copy number variation1nstd102humanUncertain significance GRCh37 chr14: 88,391,407-89,343,754 , GRCh38.p12 chr14: 87,925,063-88,877,410 LOC105370612, SPATA7, 15 more genes
    nsv7069334inversion1nstd229human GRCh38 chr14: 84,501,002-89,358,377 , GRCh37.p13 chr14: 84,967,346-89,824,721 EML5, LOC105370612, 35 more genes
    nsv7066414inversion1nstd229human GRCh38 chr14: 79,890,342-89,436,638 , GRCh37.p13 chr14: 80,356,685-89,902,982 SPATA7, RNU6ATAC28P, 82 more genes
    nsv7064896inversion1nstd229human GRCh38 chr14: 88,268,926-88,269,611 , GRCh37.p13 chr14: 88,735,270-88,735,955 KCNK10
    nsv7063560inversion1nstd229human GRCh38 chr14: 88,268,990-88,269,574 , GRCh37.p13 chr14: 88,735,334-88,735,918 KCNK10
    nsv7059378inversion1nstd229human GRCh38 chr14: 87,626,566-93,230,083 , GRCh37.p13 chr14: 88,092,910-93,674,575 PSMC1, HISLA, 87 more genes
    nsv6977479copy number variation1nstd229human GRCh38 chr14: 88,177,687-88,181,962 , GRCh37.p13 chr14: 88,644,031-88,648,306 LOC105370612, KCNK10
    nsv6976190copy number variation1nstd229human GRCh38 chr14: 88,290,271-88,310,247 , GRCh37.p13 chr14: 88,756,615-88,776,591 KCNK10
    nsv6974435copy number variation1nstd229human GRCh38 chr14: 88,167,425-88,181,849 , GRCh37.p13 chr14: 88,633,769-88,648,193 LOC105370612, KCNK10
    nsv6974122copy number variation1nstd229human GRCh38 chr14: 88,202,363-88,208,223 , GRCh37.p13 chr14: 88,668,707-88,674,567 KCNK10
    nsv6973525copy number variation1nstd229human GRCh38 chr14: 87,943,655-88,224,918 , GRCh37.p13 chr14: 88,409,999-88,691,262 GALC, KCNK10, 7 more genes
    nsv6971419copy number variation1nstd229human GRCh38 chr14: 88,310,167-88,327,576 , GRCh37.p13 chr14: 88,776,511-88,793,920 KCNK10
    nsv6970891copy number variation1nstd229human GRCh38 chr14: 88,285,505-88,289,677 , GRCh37.p13 chr14: 88,751,849-88,756,021 KCNK10
    nsv6970174copy number variation1nstd229human GRCh38 chr14: 88,273,201-88,276,600 , GRCh37.p13 chr14: 88,739,545-88,742,944 KCNK10
    nsv6968461copy number variation1nstd229human GRCh38 chr14: 88,189,609-88,191,143 , GRCh37.p13 chr14: 88,655,953-88,657,487 KCNK10
    nsv6968290copy number variation1nstd229human GRCh38 chr14: 88,274,085-88,288,416 , GRCh37.p13 chr14: 88,740,429-88,754,760 KCNK10
    nsv6964562copy number variation1nstd229human GRCh38 chr14: 88,297,070-88,297,375 , GRCh37.p13 chr14: 88,763,414-88,763,719 KCNK10
    nsv6964396copy number variation1nstd229human GRCh38 chr14: 88,216,222-88,218,420 , GRCh37.p13 chr14: 88,682,566-88,684,764 KCNK10
    nsv6963809copy number variation1nstd229human GRCh38 chr14: 88,312,566-88,425,441 , GRCh37.p13 chr14: 88,778,910-88,891,785 SPATA7, KCNK10
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