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Items: 1 to 20 of 186

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6120715copy number variation1nstd186human GRCh37 chr13: 95,248,964-95,249,503 , GRCh38.p12 chr13: 94,596,710-94,597,249 TGDS
    nsv5696263mobile element insertion1nstd211human GRCh38 chr13: 94,586,247-94,586,247 , GRCh37.p13 chr13: 95,238,501-95,238,501 TGDS
    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
    nsv5503160copy number variation1nstd206human GRCh38 chr13: 94,596,710-94,597,249 , GRCh37.p13 chr13: 95,248,964-95,249,503 TGDS
    nsv5414089mobile element insertion1nstd206human GRCh38 chr13: 94,586,247-94,586,298 , GRCh37.p13 chr13: 95,238,501-95,238,552 TGDS
    nsv5033445inversion1nstd200human GRCh38 chr13: 63,639,797-112,722,344 , GRCh37.p13 chr13: 64,213,930-113,376,658 , RPL15P18, 564 more genes
    nsv5009026copy number variation1nstd200human GRCh38 chr13: 94,502,483-94,760,662 , GRCh37.p13 chr13: 95,154,737-95,412,916 GPR180, LOC112268114, 12 more genes
    nsv4871044inversion1nstd200human GRCh37 chr13: 64,213,930-113,376,658 , GRCh38.p12 chr13: 63,639,797-112,722,344 , TUBGCP3, 564 more genes
    nsv4840256copy number variation1nstd200human GRCh37 chr13: 95,154,737-95,412,916 , GRCh38.p12 chr13: 94,502,483-94,760,662 RNA5SP36, BRD7P5, 12 more genes
    nsv4769288copy number variation1nstd102humanPathogenic GRCh37 chr13: 95,209,609-95,292,265 , GRCh38.p12 chr13: 94,557,355-94,640,011 GPR180, NDUFA3P5, 1 more genes
    nsv4708615copy number variation1nstd195human GRCh37 chr13: 95,185,001-95,290,051 , GRCh38.p12 chr13: 94,532,747-94,637,797 DCT, TGDS, 3 more genes
    nsv4676071copy number variation1nstd102humanUncertain significance GRCh37 chr13: 94,896,219-96,993,668 , GRCh38.p12 chr13: 94,243,965-96,341,414 SNORD13G, LINC00557, 33 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
    nsv4516068mobile element insertion1nstd166human GRCh37.p13 chr13: 95,224,687-95,224,687 , GRCh38.p12 chr13: 94,572,433-94,572,433 TGDS
    nsv4504276mobile element insertion1nstd166human GRCh37.p13 chr13: 95,243,092-95,243,092 , GRCh38.p12 chr13: 94,590,838-94,590,838 TGDS
    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
    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
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