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Items: 1 to 20 of 210

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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
    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
    nsv5033445inversion1nstd200human GRCh38 chr13: 63,639,797-112,722,344 , GRCh37.p13 chr13: 64,213,930-113,376,658 , RPL15P18, 564 more genes
    nsv5006995copy number variation1nstd200human GRCh38 chr13: 110,716,122-110,717,885 , GRCh37.p13 chr13: 111,368,469-111,370,232 ING1
    nsv4871044inversion1nstd200human GRCh37 chr13: 64,213,930-113,376,658 , GRCh38.p12 chr13: 63,639,797-112,722,344 , TUBGCP3, 564 more genes
    nsv4842568copy number variation1nstd200human GRCh37 chr13: 111,368,469-111,370,232 , GRCh38.p12 chr13: 110,716,122-110,717,885 ING1
    nsv4769247copy number variation1nstd201human GRCh37 chr13: 109,490,236-115,107,733 , GRCh38.p12 chr13: 108,837,888-114,342,258 , PARP1P1, 117 more genes
    nsv4729392copy number variation1nstd102humanUncertain significance GRCh37 chr13: 111,374,280-112,537,874 , GRCh38.p12 chr13: 110,721,933-111,883,560 PRECSIT, LOC107983958, 23 more genes
    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
    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
    nsv4675644copy number variation1nstd102humanPathogenic GRCh37 chr13: 96,895,656-115,107,733 , GRCh38.p12 chr13: 96,243,402-114,342,258 ZIC2, LINC03032, 266 more genes
    nsv4642510copy number variation1nstd186human GRCh37 chr13: 111,364,000-111,369,250 , GRCh38.p12 chr13: 110,711,653-110,716,903 CARS2, ING1
    nsv4621768copy number variation1nstd183human GRCh37 chr13: 111,357,835-111,372,190 , GRCh38.p12 chr13: 110,705,488-110,719,843 CARS2, ING1
    nsv4456766copy number variation1nstd102humanUncertain significance GRCh37 chr13: 111,344,288-111,384,093 , GRCh38.p12 chr13: 110,691,941-110,731,746 ING1, CARS2
    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
    nsv4456505copy number variation1nstd102humanUncertain significance GRCh37 chr13: 109,203,109-115,107,733 , GRCh38.p12 chr13: 108,550,761-114,342,258 LINC01054, GAS6-DT, 111 more genes
    nsv4456260copy number variation1nstd102humanUncertain significance GRCh37 chr13: 94,849,303-115,107,733 , GRCh38.p12 chr13: 94,197,049-114,342,258 F10, FKSG29, 300 more genes
    nsv4452838copy number variation1nstd102humannot provided GRCh37 chr13: 107,452,288-115,092,569 , GRCh38.p12 chr13: 106,799,940-114,327,094 LOC105370360, COL4A1, 122 more genes
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