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Items: 1 to 20 of 353

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7140046insertion1nstd232human GRCh37.p13 chr14: 91,952,078-91,952,078 , GRCh38.p12 chr14: 91,485,734-91,485,734 PPP4R3A
    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
    nsv7077197inversion1nstd229human GRCh38 chr14: 91,508,634-91,508,715 , GRCh37.p13 chr14: 91,974,978-91,975,059 PPP4R3A
    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
    nsv6977805copy number variation1nstd229human GRCh38 chr14: 91,486,001-91,541,400 , GRCh37.p13 chr14: 91,952,345-92,002,208 PPP4R3A, LOC101928957
    nsv6974185copy number variation1nstd229human GRCh38 chr14: 91,500,585-91,504,947 , GRCh37.p13 chr14: 91,966,929-91,971,291 PPP4R3A
    nsv6964548copy number variation1nstd229human GRCh38 chr14: 91,486,101-91,580,600 , GRCh37.p13 chr14: 91,952,445-92,002,208 CATSPERB, PPP4R3A, 1 more genes
    nsv6962754copy number variation1nstd229human GRCh38 chr14: 91,506,028-91,543,168 , GRCh37.p13 chr14: 91,972,372-92,002,208 PPP4R3A, LOC101928957
    nsv6958459copy number variation1nstd229human GRCh38 chr14: 91,493,201-91,494,000 , GRCh37.p13 chr14: 91,959,545-91,960,344 PPP4R3A
    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
    nsv6592963inversion1nstd223human GRCh38 chr14: 86,486,184-95,139,000 , GRCh37.p13 chr14: 86,952,528-95,605,337 CCDC88C-DT, RPSAP4, 134 more genes
    nsv6591551inversion1nstd223human GRCh38 chr14: 91,074,052-93,300,799 , GRCh37.p13 chr14: 91,540,396-93,674,575 LINC02287, LGMN, 39 more genes
    nsv6590318inversion1nstd223human GRCh38 chr14: 91,472,137-91,472,389 , GRCh37.p13 chr14: 91,938,481-91,938,733 PPP4R3A
    nsv6589024inversion1nstd223human GRCh38 chr14: 91,471,952-91,472,771 , GRCh37.p13 chr14: 91,938,296-91,939,115 PPP4R3A
    nsv6586723inversion1nstd223human GRCh38 chr14: 91,499,766-91,500,470 , GRCh37.p13 chr14: 91,966,110-91,966,814 PPP4R3A
    nsv6586085inversion1nstd223human GRCh38 chr14: 91,459,161-91,459,837 , GRCh37.p13 chr14: 91,925,505-91,926,181 PPP4R3A
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