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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5672807copy number variation1nstd102humanPathogenic GRCh37 chr13: 92,002,837-103,343,314 , GRCh38.p12 chr13: 91,350,583-102,690,964 RPL7L1P12, MIR548AS, 153 more genes
    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
    nsv5511750copy number variation1nstd206human GRCh38 chr13: 98,640,744-98,642,653 , GRCh37.p13 chr13: 99,292,998-99,294,907 CALM2P4
    nsv5154545mobile element insertion1nstd203human GRCh38 chr13: 98,641,704-98,641,724 , GRCh37.p13 chr13: 99,293,958-99,293,978 CALM2P4
    nsv5033445inversion1nstd200human GRCh38 chr13: 63,639,797-112,722,344 , GRCh37.p13 chr13: 64,213,930-113,376,658 , RPL15P18, 564 more genes
    nsv4993906copy number variation1nstd200human GRCh38 chr13: 98,640,877-98,642,991 , GRCh37.p13 chr13: 99,293,131-99,295,245 CALM2P4
    nsv4871044inversion1nstd200human GRCh37 chr13: 64,213,930-113,376,658 , GRCh38.p12 chr13: 63,639,797-112,722,344 , TUBGCP3, 564 more genes
    nsv4830097copy number variation1nstd200human GRCh37 chr13: 99,293,131-99,295,246 , GRCh38.p12 chr13: 98,640,877-98,642,992 CALM2P4
    nsv4704415copy number variation1nstd195human GRCh37 chr13: 99,258,551-99,386,951 , GRCh38.p12 chr13: 98,606,297-98,734,697 SLC15A1, CYCSP35, 3 more genes
    nsv4675892copy number variation1nstd102humanPathogenic GRCh37 chr13: 96,240,346-106,103,782 , GRCh38.p12 chr13: 95,588,092-105,451,433 LOC105370328, LINC00554, 132 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
    nsv4672380copy number variation1nstd186human GRCh37 chr13: 99,293,018-99,294,863 , GRCh38.p12 chr13: 98,640,764-98,642,609 CALM2P4
    nsv4599216copy number variation1nstd183human GRCh37 chr13: 99,293,018-99,294,863 , GRCh38.p12 chr13: 98,640,764-98,642,609 CALM2P4
    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
    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
    nsv3970252insertion1nstd168human GRCh38 chr13: 98,592,837-98,682,271 , GRCh37.p13 chr13: 99,245,091-99,334,525 SLC15A1, CYCSP35, 3 more genes
    nsv3924676copy number variation1nstd102humanPathogenic GRCh38 chr13: 18,456,040-114,340,285 , GRCh37 chr13: 19,030,180-115,105,760 , NCBI36 chr13: 17,928,180-114,123,862 GRTP1, FABP5P1, 1334 more genes
    nsv3924528copy number variation1nstd102humanPathogenic GRCh37 chr13: 41,516,434-115,085,141 , GRCh38 chr13: 40,942,298-114,340,331 , NCBI36 chr13: 40,414,434-114,123,908 LOC105370271, OR7E33P, 925 more genes
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