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Items: 1 to 20 of 355

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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
    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
    nsv6977861copy number variation1nstd229human GRCh38 chr14: 91,784,901-91,802,300 , GRCh37.p13 chr14: 92,251,245-92,268,644 TC2N
    nsv6976262copy number variation1nstd229human GRCh38 chr14: 91,733,097-91,800,134 , GRCh37.p13 chr14: 92,199,441-92,266,478 TC2N
    nsv6971150copy number variation1nstd229human GRCh38 chr14: 91,778,918-91,779,727 , GRCh37.p13 chr14: 92,245,262-92,246,071 TC2N
    nsv6963728copy number variation1nstd229human GRCh38 chr14: 91,839,274-91,842,670 , GRCh37.p13 chr14: 92,305,618-92,309,014 TC2N
    nsv6959535copy number variation1nstd229human GRCh38 chr14: 91,815,005-91,820,941 , GRCh37.p13 chr14: 92,281,349-92,287,285 TC2N
    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
    nsv6593656inversion1nstd223human GRCh38 chr14: 91,822,743-91,823,244 , GRCh37.p13 chr14: 92,289,087-92,289,588 TC2N
    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
    nsv6576886inversion1nstd223human GRCh38 chr14: 87,626,564-93,230,084 , GRCh37.p13 chr14: 88,092,908-93,674,575 ATXN3, RIN3, 87 more genes
    nsv6576568inversion1nstd223human GRCh38 chr14: 91,779,124-91,779,691 , GRCh37.p13 chr14: 92,245,468-92,246,035 TC2N
    nsv6513320copy number variation1nstd223human GRCh38 chr14: 91,831,801-91,840,300 , GRCh37.p13 chr14: 92,298,145-92,306,644 TC2N
    nsv6511361copy number variation1nstd223human GRCh38 chr14: 91,826,401-91,827,200 , GRCh37.p13 chr14: 92,292,745-92,293,544 TC2N
    nsv6510012copy number variation1nstd223human GRCh38 chr14: 91,811,221-91,811,735 , GRCh37.p13 chr14: 92,277,565-92,278,079 TC2N
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