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Items: 1 to 20 of 167

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5684195mobile element insertion1nstd211human GRCh38 chr6: 49,525,109-49,525,109 , GRCh37.p13 chr6: 49,492,822-49,492,822 GLYATL3
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5040265inversion1nstd200human GRCh38 chr6: 49,481,877-49,812,356 , GRCh37.p13 chr6: 49,449,590-49,780,069 PGK2, RHAG, 7 more genes
    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
    nsv4598622copy number variation1nstd183human GRCh37 chr6: 49,431,569-49,466,791 , GRCh38.p12 chr6: 49,463,856-49,499,078 CENPQ, GLYATL3
    nsv4498010mobile element insertion1nstd166human GRCh37.p13 chr6: 49,469,240-49,469,240 , GRCh38.p12 chr6: 49,501,527-49,501,527 GLYATL3
    nsv4496009mobile element insertion1nstd166human GRCh37.p13 chr6: 49,467,514-49,467,514 , GRCh38.p12 chr6: 49,499,801-49,499,801 GLYATL3
    nsv4456000copy number variation1nstd102humanUncertain significance GRCh37 chr6: 48,617,762-49,836,065 , GRCh38.p12 chr6: 48,650,026-49,868,352 LOC100421158, EEF1A1P42, 14 more genes
    nsv4395505copy number variation1nstd174human GRCh37 chr6: 49,431,569-49,470,663 , GRCh38.p12 chr6: 49,463,856-49,502,950 CENPQ, GLYATL3
    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
    nsv4148940copy number variation1nstd166human GRCh37.p13 chr6: 49,485,229-49,485,442 , GRCh38.p12 chr6: 49,517,516-49,517,729 GLYATL3
    nsv4146594copy number variation1nstd166human GRCh37.p13 chr6: 49,470,000-49,476,000 , GRCh38.p12 chr6: 49,502,287-49,508,287 GLYATL3
    nsv4135712copy number variation1nstd166human GRCh37.p13 chr6: 49,481,647-49,507,207 , GRCh38.p12 chr6: 49,513,934-49,539,494 GLYATL3
    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
    nsv3918622copy number variation1nstd102humanUncertain significance NCBI36 chr6: 49,497,464-49,653,124 , GRCh37.p13 chr6: 49,389,505-49,545,165 , GRCh38.p12 chr6: 49,421,792-49,577,452 C6orf141, CENPQ, 3 more genes
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