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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5941465copy number variation1nstd209human GRCh38 chr13: 79,424,298-79,424,495 , GRCh37.p13 chr13: 79,998,433-79,998,630 LOC105370274, RBM26-AS1
    nsv5932186copy number variation1nstd209human GRCh38 chr13: 77,934,881-83,910,012 , GRCh37.p13 chr13: 78,509,016-84,484,147 NDFIP2, LINC01068, 54 more genes
    nsv5929133copy number variation1nstd209human GRCh38 chr13: 79,419,091-79,419,228 , GRCh37.p13 chr13: 79,993,226-79,993,363 RBM26-AS1
    nsv5590716copy number variation1nstd207human GRCh38 chr13: 79,419,091-79,419,159 , GRCh37.p13 chr13: 79,993,226-79,993,294 RBM26-AS1
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5508579copy number variation1nstd206human GRCh38 chr13: 79,423,636-79,426,141 , GRCh37.p13 chr13: 79,997,771-80,000,276 RBM26-AS1, LOC105370274
    nsv5497911copy number variation1nstd206human GRCh38 chr13: 79,424,301-79,424,496 , GRCh37.p13 chr13: 79,998,436-79,998,631 RBM26-AS1, LOC105370274
    nsv5496444copy number variation1nstd206human GRCh38 chr13: 79,199,129-79,520,920 , GRCh37.p13 chr13: 79,773,264-80,095,055 NDFIP2, RBM26, 4 more genes
    nsv5341367translocation1nstd200human GRCh37 chr13: 79,998,631-79,998,631 , GRCh37 chr13: 79,998,436-79,998,436 , GRCh38.p12 chr13: 79,424,301-79,424,301 , GRCh38.p12 chr13: 79,424,496-79,424,496 RBM26-AS1, LOC105370274
    nsv5033445inversion1nstd200human GRCh38 chr13: 63,639,797-112,722,344 , GRCh37.p13 chr13: 64,213,930-113,376,658 , RPL15P18, 564 more genes
    nsv4997599copy number variation1nstd200human GRCh38 chr13: 79,412,789-79,421,479 , GRCh37.p13 chr13: 79,986,924-79,995,614 RBM26-AS1, LOC105370274
    nsv4871044inversion1nstd200human GRCh37 chr13: 64,213,930-113,376,658 , GRCh38.p12 chr13: 63,639,797-112,722,344 , TUBGCP3, 564 more genes
    nsv4832138copy number variation1nstd200human GRCh37 chr13: 79,982,406-79,983,892 , GRCh38.p12 chr13: 79,408,271-79,409,757 RBM26-AS1
    nsv4745932copy number variation1nstd199human GRCh37 chr13: 79,993,218-79,993,289 , GRCh38.p12 chr13: 79,419,083-79,419,154 RBM26-AS1
    nsv4675995copy number variation1nstd102humanPathogenic GRCh37 chr13: 51,512,603-91,631,111 , GRCh38.p12 chr13: 50,938,467-90,978,857 RNU7-88P, LINC00564, 396 more genes
    nsv4675850copy number variation1nstd102humanPathogenic GRCh37 chr13: 53,262,013-115,107,733 , GRCh38.p12 chr13: 52,687,878-114,342,258 TEX30, LOC101927712, 680 more genes
    nsv4675244copy number variation1nstd102humanPathogenic GRCh37 chr13: 71,502,357-86,571,730 , GRCh38.p12 chr13: 70,928,225-85,997,595 RNU6-79P, LINC01069, 151 more genes
    nsv4456768copy number variation1nstd102humanUncertain significance GRCh37 chr13: 79,164,755-80,568,672 , GRCh38.p12 chr13: 78,590,620-79,994,537 RNA5SP33, LOC105370272, 20 more genes
    nsv4456561copy number variation1nstd102humanPathogenic GRCh37 chr13: 61,775,567-115,107,733 , GRCh38.p12 chr13: 61,201,433-114,342,258 LOC105370262, LINC01080, 609 more genes
    nsv4455966copy number variation1nstd102humanUncertain significance GRCh37 chr13: 79,744,183-80,830,079 , GRCh38.p12 chr13: 79,170,048-80,255,944 LINC01038, LINC00382, 10 more genes
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