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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5845532copy number variation1nstd209human GRCh38 chr6: 49,962,366-49,967,909 , GRCh37.p13 chr6: 49,930,079-49,935,622 DEFB113, DEFB114
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5473510copy number variation1nstd206human GRCh38 chr6: 49,961,984-49,962,111 , GRCh37.p13 chr6: 49,929,697-49,929,824 DEFB114
    nsv5362957translocation1nstd200human GRCh38 chr6: 49,962,111-49,962,111 , GRCh38 chr6: 49,961,984-49,961,984 , GRCh37.p13 chr6: 49,929,824-49,929,824 , GRCh37.p13 chr6: 49,929,697-49,929,697 DEFB114
    nsv5221557copy number variation1nstd204human GRCh38.p13 chr6: 49,961,101-49,967,900 , GRCh37.p13 chr6: 49,928,814-49,935,613 DEFB114, DEFB113
    nsv5104772mobile element insertion1nstd203human GRCh38 chr6: 49,962,286-49,962,305 , GRCh37.p13 chr6: 49,929,999-49,930,018 DEFB114
    nsv4941362copy number variation1nstd200human GRCh38 chr6: 49,962,981-49,971,925 , GRCh37.p13 chr6: 49,930,694-49,939,638 DEFB113, DEFB114
    nsv4816356copy number variation1nstd200human GRCh37 chr6: 49,929,697-49,929,824 , GRCh38.p12 chr6: 49,961,984-49,962,111 DEFB114
    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
    nsv4729270copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 48,626,041-55,575,545 , GRCh38.p12 chr6: 48,658,305-55,710,747 CRISP1, SLC25A20P1, 105 more genes
    nsv4729154copy number variation1nstd102humanUncertain significance GRCh37 chr6: 48,566,675-50,063,411 , GRCh38.p12 chr6: 48,598,939-50,095,698 MMUT, RHAG, 21 more genes
    nsv4675491copy number variation1nstd102humanUncertain significance GRCh37 chr6: 49,459,881-50,024,153 , GRCh38.p12 chr6: 49,492,168-50,056,440 LOC101927048, GLYATL3, 14 more genes
    nsv4493810mobile element insertion1nstd166human GRCh37.p13 chr6: 49,928,696-49,928,696 , GRCh38.p12 chr6: 49,960,983-49,960,983 DEFB114
    nsv4488630mobile element insertion1nstd166human GRCh37.p13 chr6: 49,929,999-49,929,999 , GRCh38.p12 chr6: 49,962,286-49,962,286 DEFB114
    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
    nsv4143708copy number variation1nstd166human GRCh37.p13 chr6: 49,929,697-49,929,824 , GRCh38.p12 chr6: 49,961,984-49,962,111 DEFB114
    nsv3923721copy number variation1nstd102humanPathogenic GRCh38 chr6: 45,681,671-54,212,044 , GRCh37 chr6: 45,649,408-54,076,842 , NCBI36 chr6: 45,757,386-54,184,801 PAQR8, GSTA6P, 131 more genes
    nsv3913758copy number variation1nstd102humanLikely pathogenic NCBI36 chr6: 47,267,474-51,400,063 , GRCh37 chr6: 47,159,515-51,292,104 , GRCh38 chr6: 47,191,779-51,427,306 CRISP1, FTH1P5, 46 more genes
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