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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146016copy number variation1nstd232human GRCh37.p13 chr2: 44,200,853-44,200,932 , GRCh38.p12 chr2: 43,973,714-43,973,793 LRPPRC
    nsv7143281insertion1nstd232human GRCh37.p13 chr2: 44,145,537-44,145,537 , GRCh38.p12 chr2: 43,918,398-43,918,398 LRPPRC
    nsv7142003copy number variation1nstd232human GRCh37.p13 chr2: 44,204,189-44,204,290 , GRCh38.p12 chr2: 43,977,050-43,977,151 LRPPRC
    nsv7139157insertion1nstd232human GRCh37.p13 chr2: 44,174,509-44,174,509 , GRCh38.p12 chr2: 43,947,370-43,947,370 LRPPRC
    nsv7098993copy number variation1nstd102humanPathogenic GRCh38 chr2: 43,986,415-44,009,956 , GRCh37.p13 chr2: 44,213,554-44,237,095 LRPPRC
    nsv7096656copy number variation1nstd102humanUncertain significance GRCh37 chr2: 44,200,726-44,204,435 , GRCh38.p12 chr2: 43,973,587-43,977,296 LRPPRC
    nsv7096653copy number variation1nstd102humanUncertain significance GRCh37 chr2: 38,121,051-47,710,088 , GRCh38.p12 chr2: 37,893,908-47,482,949 PLEKHH2, RNU6-566P, 151 more genes
    nsv7096640copy number variation1nstd102humanPathogenic GRCh37 chr2: 44,184,514-44,187,783 , GRCh38.p12 chr2: 43,957,375-43,960,644 LRPPRC
    nsv7096639copy number variation2nstd102humanUncertain significance GRCh37 chr2: 44,001,278-44,209,593 , GRCh38.p12 chr2: 43,774,139-43,982,454 LOC105374571, RNU6-1048P, 6 more genes
    nsv7096505copy number variation1nstd102humanPathogenic GRCh37 chr2: 44,209,367-44,223,096 , GRCh38.p12 chr2: 43,982,228-43,995,957 LRPPRC
    nsv7096162copy number variation1nstd102humanPathogenic GRCh37 chr2: 44,184,514-44,190,855 , GRCh38.p12 chr2: 43,957,375-43,963,716 LRPPRC
    nsv7096161copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 44,143,180-44,145,434 , GRCh38.p12 chr2: 43,916,041-43,918,295 LRPPRC
    nsv7093548insertion1nstd102humanPathogenic GRCh37 chr2: 44,174,428-44,174,428 , GRCh38 chr2: 43,947,289-43,947,289 LRPPRC
    nsv7093455delins1nstd102humanLikely pathogenic GRCh38 chr2: 43,982,203-43,982,285 , GRCh37 chr2: 44,209,342-44,209,424 LRPPRC
    nsv7049173inversion1nstd229human GRCh38 chr2: 43,898,072-43,898,183 , GRCh37.p13 chr2: 44,125,211-44,125,322 LRPPRC
    nsv7039759inversion1nstd229human GRCh38 chr2: 39,986,388-47,339,194 , GRCh37.p13 chr2: 40,213,528-47,566,333 RPL36AP14, CRIPT, 105 more genes
    nsv6677615copy number variation1nstd229human GRCh38 chr2: 43,817,923-43,901,048 , GRCh37.p13 chr2: 44,045,062-44,128,187 LRPPRC, ABCG5, 4 more genes
    nsv6676797copy number variation1nstd229human GRCh38 chr2: 43,763,317-44,075,069 , GRCh37.p13 chr2: 43,990,456-44,302,208 ABCG8, LOC102725159, 8 more genes
    nsv6673389copy number variation1nstd229human GRCh38 chr2: 43,945,467-43,945,519 , GRCh37.p13 chr2: 44,172,606-44,172,658 LRPPRC
    nsv6673088copy number variation1nstd229human GRCh38 chr2: 43,948,040-43,948,411 , GRCh37.p13 chr2: 44,175,179-44,175,550 LRPPRC
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