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Items: 1 to 20 of 118

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5526554copy number variation1nstd206human GRCh38 chr19: 43,719,050-43,731,363 , GRCh37.p13 chr19: 44,223,202-44,235,515 SMG9, IRGC
    nsv5519518copy number variation1nstd206human GRCh38 chr19: 43,743,709-43,743,775 , GRCh37.p13 chr19: 44,247,861-44,247,927 SMG9
    nsv5162411mobile element insertion1nstd203human GRCh38 chr19: 43,741,942-43,741,985 , GRCh37.p13 chr19: 44,246,094-44,246,137 SMG9
    nsv4678976copy number variation1nstd189human GRCh37.p13 chr19: 44,188,628-44,507,055 , GRCh38.p12 chr19: 43,684,476-44,002,903 KCNN4, ZNF45, 11 more genes
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4371631copy number variation1nstd173human GRCh37 chr19: 44,133,648-44,247,651 , GRCh38.p12 chr19: 43,629,496-43,743,499 , IRGC, 6 more genes
    nsv4365671copy number variation1nstd173human GRCh37 chr19: 44,133,648-44,247,663 , GRCh38.p12 chr19: 43,629,496-43,743,511 , PLAUR, 6 more genes
    nsv4267882copy number variation1nstd166human GRCh37.p13 chr19: 44,246,181-44,246,261 , GRCh38.p12 chr19: 43,742,029-43,742,109 SMG9
    nsv4256968copy number variation1nstd166human GRCh37.p13 chr19: 44,230,239-44,230,466 , GRCh38.p12 chr19: 43,726,087-43,726,314 SMG9
    nsv3920763copy number variation1nstd102humanUncertain significance NCBI36 chr19: 48,534,223-49,049,155 , GRCh38 chr19: 43,338,231-43,853,163 , GRCh37 chr19: 43,842,383-44,357,315 SRRM5, RN7SL368P, 23 more genes
    nsv3913730copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354 BCKDHA, ADGRE5, 1102 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 BABAM1, BEST2, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 LENG8, SYDE1, 2408 more genes
    nsv3891669copy number variation1nstd102humanPathogenic GRCh37 chr19: 43,013,365-47,241,534 , GRCh38.p12 chr19: 42,509,213-46,738,277 MIR320E, BCL3, 189 more genes
    nsv3880735copy number variation1nstd102humanLikely pathogenic GRCh38 chr19: 41,608,672-44,315,856 , GRCh37.p13 chr19: 42,514,712-44,820,009 ATP1A3, CEACAM1, 114 more genes
    nsv3198545complex substitution1nstd152human GRCh38 chr19: 43,746,813-43,747,071 , GRCh37.p13 chr19: 44,250,965-44,251,223 SMG9
    nsv3168446copy number variation1nstd158human GRCh37 chr19: 35,445,908-45,506,757 , GRCh38.p12 chr19: 34,955,004-45,003,499 , ACTN4, 449 more genes
    nsv3161644copy number variation1nstd151human GRCh37 chr19: 44,251,591-44,254,898 , GRCh38.p12 chr19: 43,747,439-43,750,746 SMG9
    nsv2757532copy number variation1nstd130human GRCh37 chr19: 266,034-54,723,310 , GRCh38.p12 chr19: 266,034-54,071,460 , BABAM1, 2197 more genes
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