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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5672796copy number variation1nstd102humanPathogenic GRCh37 chr13: 94,679,977-111,536,145 , GRCh38.p12 chr13: 94,027,723-110,883,798 LINC00359, LOC107984609, 220 more genes
    nsv5653859insertion1nstd207human GRCh38 chr13: 110,530,184-110,530,184 , GRCh37.p13 chr13: 111,182,531-111,182,531 RAB20
    nsv5644594insertion1nstd207human GRCh38 chr13: 110,530,340-110,530,340 , GRCh37.p13 chr13: 111,182,687-111,182,687 RAB20
    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
    nsv5560567sequence alteration1nstd206human GRCh38 chr13: 109,802,242-110,580,747 , GRCh37.p13 chr13: 110,454,589-111,233,094 , COL4A2, 12 more genes
    nsv5509957copy number variation1nstd206human GRCh38 chr13: 110,538,793-110,539,843 , GRCh37.p13 chr13: 111,191,140-111,192,190 RAB20
    nsv5158722mobile element insertion1nstd203human GRCh38 chr13: 110,551,082-110,551,097 , GRCh37.p13 chr13: 111,203,429-111,203,444 RAB20
    nsv5033445inversion1nstd200human GRCh38 chr13: 63,639,797-112,722,344 , GRCh37.p13 chr13: 64,213,930-113,376,658 , RPL15P18, 564 more genes
    nsv5006985copy number variation1nstd200human GRCh38 chr13: 110,516,876-110,522,420 , GRCh37.p13 chr13: 111,169,223-111,174,767 RAB20
    nsv4993989copy number variation1nstd200human GRCh38 chr13: 110,514,328-110,681,153 , GRCh37.p13 chr13: 111,166,675-111,333,500 NAXD, RAB20, 1 more genes
    nsv4871044inversion1nstd200human GRCh37 chr13: 64,213,930-113,376,658 , GRCh38.p12 chr13: 63,639,797-112,722,344 , TUBGCP3, 564 more genes
    nsv4832993copy number variation1nstd200human GRCh37 chr13: 111,166,675-111,333,500 , GRCh38.p12 chr13: 110,514,328-110,681,153 RAB20, NAXD, 1 more genes
    nsv4769247copy number variation1nstd201human GRCh37 chr13: 109,490,236-115,107,733 , GRCh38.p12 chr13: 108,837,888-114,342,258 , PARP1P1, 117 more genes
    nsv4757984insertion1nstd199human GRCh37 chr13: 111,182,547-111,182,547 , GRCh38.p12 chr13: 110,530,200-110,530,200 RAB20
    nsv4729275copy number variation1nstd102humanUncertain significance GRCh37 chr13: 109,752,674-112,352,804 , GRCh38.p12 chr13: 109,100,326-111,700,457 ANKRD10, CARS2, 46 more genes
    nsv4728884copy number variation1nstd102humanPathogenic GRCh37 chr13: 106,256,198-115,107,733 , GRCh38.p12 chr13: 105,603,849-114,342,258 LINC01044, CARS2, 139 more genes
    nsv4728419copy number variation1nstd102humanPathogenic GRCh37 chr13: 102,175,801-115,169,858 , GRCh38.p12 chr13: 101,523,450-114,344,403 RPL7P45, LOC107984615, 182 more genes
    nsv4683605copy number variation1nstd102humanUncertain significance GRCh37 chr13: 110,960,251-111,358,440 , GRCh38.p12 chr13: 110,307,904-110,706,093 RAB20, COL4A2-AS2, 5 more genes
    nsv4681417copy number variation2nstd102humanUncertain significance GRCh37 chr13: 111,102,026-111,176,544 , GRCh38.p12 chr13: 110,449,679-110,524,197 COL4A2-AS2, COL4A2, 2 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
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