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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141431insertion1nstd232human GRCh37.p13 chr13: 49,002,557-49,002,557 , GRCh38.p12 chr13: 48,428,421-48,428,421 RB1, LPAR6
    nsv7074086inversion1nstd229human GRCh38 chr13: 47,957,386-48,970,527 , GRCh37.p13 chr13: 48,531,521-49,544,663 SUCLA2, PPP1R26P1, 17 more genes
    nsv7073451inversion1nstd229human GRCh38 chr13: 39,843,646-49,674,098 , GRCh37.p13 chr13: 40,417,783-50,248,234 CYCSP34, FNDC3A, 195 more genes
    nsv6957956copy number variation1nstd229human GRCh38 chr13: 48,430,084-48,431,560 , GRCh37.p13 chr13: 49,004,220-49,005,696 RB1, LPAR6
    nsv6957513copy number variation1nstd229human GRCh38 chr13: 48,403,992-48,406,794 , GRCh37.p13 chr13: 48,978,128-48,980,930 LPAR6, RB1
    nsv6952471copy number variation1nstd229human GRCh38 chr13: 48,218,502-48,686,659 , GRCh37.p13 chr13: 48,792,638-49,260,795 RCBTB2, RB1, 10 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
    nsv6952021copy number variation1nstd229human GRCh38 chr13: 48,443,699-48,450,367 , GRCh37.p13 chr13: 49,017,835-49,024,503 RB1, LPAR6
    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
    nsv6951122copy number variation1nstd229human GRCh38 chr13: 48,403,835-48,408,895 , GRCh37.p13 chr13: 48,977,971-48,983,031 LPAR6, RB1
    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
    nsv6945941copy number variation1nstd229human GRCh38 chr13: 48,429,607-48,438,076 , GRCh37.p13 chr13: 49,003,743-49,012,212 LPAR6, RB1
    nsv6944419copy number variation1nstd229human GRCh38 chr13: 48,402,975-48,405,415 , GRCh37.p13 chr13: 48,977,111-48,979,551 RB1, LPAR6
    nsv6943858copy number variation1nstd229human GRCh38 chr13: 48,441,753-48,441,782 , GRCh37.p13 chr13: 49,015,889-49,015,918 RB1, LPAR6
    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
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6582005inversion1nstd223human GRCh38 chr13: 48,434,020-48,434,223 , GRCh37.p13 chr13: 49,008,156-49,008,359 LPAR6, RB1
    nsv6581956inversion1nstd223human GRCh38 chr13: 48,433,937-48,434,296 , GRCh37.p13 chr13: 49,008,073-49,008,432 LPAR6, RB1
    nsv6578747inversion1nstd223human GRCh38 chr13: 48,414,069-48,415,579 , GRCh37.p13 chr13: 48,988,205-48,989,715 LPAR6, RB1
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