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Items: 1 to 20 of 212

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073451inversion1nstd229human GRCh38 chr13: 39,843,646-49,674,098 , GRCh37.p13 chr13: 40,417,783-50,248,234 CYCSP34, FNDC3A, 195 more genes
    nsv7070621inversion1nstd229human GRCh38 chr13: 49,320,428-51,629,920 , GRCh37.p13 chr13: 49,894,564-52,204,056 MIR3613, RNASEH2B-AS1, 50 more genes
    nsv7068506inversion1nstd229human GRCh38 chr13: 49,621,129-49,626,530 , GRCh37.p13 chr13: 50,195,265-50,200,666 ARL11, LOC105370204
    nsv7062591inversion1nstd229human GRCh38 chr13: 49,445,029-50,859,553 , GRCh37.p13 chr13: 50,019,165-51,433,689 PHF11, RPL34P26, 28 more genes
    nsv6957561copy number variation1nstd229human GRCh38 chr13: 49,145,001-51,117,700 , GRCh37.p13 chr13: 49,719,137-51,691,836 TRIM13, EBPL, 40 more genes
    nsv6956158copy number variation1nstd229human GRCh38 chr13: 49,629,088-49,629,246 , GRCh37.p13 chr13: 50,203,224-50,203,382 ARL11
    nsv6953234copy number variation1nstd229human GRCh38 chr13: 49,610,822-50,909,481 , GRCh37.p13 chr13: 50,184,958-51,483,617 KCNRG, RNA5SP28, 24 more genes
    nsv6952872copy number variation1nstd229human GRCh38 chr13: 49,496,001-49,792,600 , GRCh37.p13 chr13: 50,070,137-50,366,736 PHF11, RCBTB1, 6 more genes
    nsv6952435copy number variation1nstd229human GRCh38 chr13: 48,165,561-51,834,243 , GRCh37.p13 chr13: 48,739,697-52,408,379 LPAR6, RNY4P30, 77 more genes
    nsv6952289copy number variation1nstd229human GRCh38 chr13: 46,982,261-52,142,641 , GRCh37.p13 chr13: 47,556,396-52,716,777 KCNRG, RNA5SP28, 99 more genes
    nsv6952184copy number variation1nstd229human GRCh38 chr13: 49,403,601-50,069,700 , GRCh37.p13 chr13: 49,977,737-50,643,836 CTAGE10P, RNY4P9, 19 more genes
    nsv6951969copy number variation1nstd229human GRCh38 chr13: 45,143,357-52,624,108 , GRCh37.p13 chr13: 45,717,492-53,198,243 SNRPGP14, EBPL, 158 more genes
    nsv6950751copy number variation1nstd229human GRCh38 chr13: 49,597,008-49,631,199 , GRCh37.p13 chr13: 50,171,144-50,205,335 ARL11, LOC105370204
    nsv6948938copy number variation1nstd229human GRCh38 chr13: 49,617,570-49,634,561 , GRCh37.p13 chr13: 50,191,706-50,208,697 LOC105370205, LOC105370204, 1 more genes
    nsv6947937copy number variation1nstd229human GRCh38 chr13: 48,313,660-50,916,452 , GRCh37.p13 chr13: 48,887,796-51,490,588 MIR16-1, PCNPP5, 51 more genes
    nsv6947585copy number variation1nstd229human GRCh38 chr13: 48,556,959-51,460,180 , GRCh37.p13 chr13: 49,131,095-52,034,316 RNY4P9, GUCY1B2, 57 more genes
    nsv6947205copy number variation1nstd229human GRCh38 chr13: 49,567,576-49,844,002 , GRCh37.p13 chr13: 50,141,712-50,418,138 EBPL, LOC105370204, 4 more genes
    nsv6944138copy number variation1nstd229human GRCh38 chr13: 49,633,124-51,990,526 , GRCh37.p13 chr13: 50,207,260-52,564,662 LOC107984561, RPL5P31, 50 more genes
    nsv6942711copy number variation1nstd229human GRCh38 chr13: 47,954,978-51,016,028 , GRCh37.p13 chr13: 48,529,113-51,590,164 COX7CP1, CTAGE10P, 60 more genes
    nsv6637547copy number variation1nstd102humanUncertain significance GRCh37 chr13: 49,888,733-50,238,594 , GRCh38.p12 chr13: 49,314,597-49,664,458 SETDB2-PHF11, LOC105370204, 8 more genes
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