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Items: 1 to 20 of 128

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097826copy number variation1nstd102humanPathogenic GRCh37 chr6: 41,126,341-43,752,536 , GRCh38.p12 chr6: 41,158,603-43,784,799 USP49, PRICKLE4, 96 more genes
    nsv7097825copy number variation1nstd102humanUncertain significance GRCh37 chr6: 41,126,341-43,737,486 , GRCh38.p12 chr6: 41,158,603-43,769,749 DNPH1, LOC107986596, 96 more genes
    nsv7043293inversion1nstd229human GRCh38 chr6: 39,854,165-43,261,822 , GRCh37.p13 chr6: 39,821,941-43,229,560 RPL23P6, RPL32P15, 95 more genes
    nsv6789272copy number variation1nstd229human GRCh38 chr6: 41,897,601-42,523,500 , GRCh37.p13 chr6: 41,865,339-42,491,238 LOC105375061, RPL36AP5, 13 more genes
    nsv6185557copy number variation1nstd214human GRCh38 chr6: 41,918,540-41,918,673 , GRCh37.p13 chr6: 41,886,278-41,886,411 MED20
    nsv6135921copy number variation1nstd213human GRCh37 chr6: 34,700,000-52,650,001 , GRCh38.p12 chr6: 34,732,223-52,785,203 ACTG1P9, CRISP1, 361 more genes
    nsv6065545insertion1nstd212human GRCh38 chr6: 41,911,491-41,911,491 , GRCh37.p13 chr6: 41,879,229-41,879,229 MED20
    nsv5903214copy number variation1nstd209human GRCh38 chr6: 41,904,100-41,904,289 , GRCh37.p13 chr6: 41,871,838-41,872,027 MED20
    nsv5845607copy number variation1nstd209human GRCh38 chr6: 41,910,256-41,912,009 , GRCh37.p13 chr6: 41,877,994-41,879,747 MED20
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5115957mobile element insertion1nstd203human GRCh38 chr6: 41,918,541-41,918,578 , GRCh37.p13 chr6: 41,886,279-41,886,316 MED20
    nsv5111430mobile element insertion1nstd203human GRCh38 chr6: 41,918,969-41,918,991 , GRCh37.p13 chr6: 41,886,707-41,886,729 MED20
    nsv5104865mobile element insertion1nstd203human GRCh38 chr6: 41,918,663-41,918,681 , GRCh37.p13 chr6: 41,886,401-41,886,419 MED20
    nsv4816162copy number variation1nstd200human GRCh37 chr6: 41,882,915-41,883,085 , GRCh38.p12 chr6: 41,915,177-41,915,347 MED20
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4735754copy number variation1nstd199human GRCh37 chr6: 26,776,020-58,144,810 , GRCh38.p12 chr6: 26,823,536-61,119,912 , RNU6-250P, 1075 more genes
    nsv4592651copy number variation1nstd183human GRCh37 chr6: 41,758,583-41,983,007 , GRCh38.p12 chr6: 41,790,845-42,015,269 , BYSL, 4 more genes
    nsv4350067copy number variation1nstd102humanPathogenic GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650 HLA-DPB2, CIMIP3, 1001 more genes
    nsv4135005copy number variation1nstd166human GRCh37.p13 chr6: 41,877,798-41,877,850 , GRCh38.p12 chr6: 41,910,060-41,910,112 MED20
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