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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
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5119188mobile element insertion1nstd203human GRCh38 chr6: 53,099,076-53,099,090 , GRCh37.p13 chr6: 52,963,874-52,963,888 FBXO9
    nsv4816419copy number variation1nstd200human GRCh37 chr6: 52,921,949-52,922,270 , GRCh38.p12 chr6: 53,057,151-53,057,472 FBXO9, CILK1
    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
    nsv4743473copy number variation1nstd199human GRCh37 chr6: 52,928,598-52,928,747 , GRCh38.p12 chr6: 53,063,800-53,063,949 FBXO9
    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
    nsv4729393copy number variation1nstd102humanUncertain significance GRCh37 chr6: 52,657,712-53,622,715 , GRCh38.p12 chr6: 52,792,914-53,757,917 KILH, GSTA6P, 29 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
    nsv4675080copy number variation1nstd102humanUncertain significance GRCh37 chr6: 52,810,337-53,016,306 , GRCh38.p12 chr6: 52,945,539-53,151,508 GSTA4, CILK1, 5 more genes
    nsv4544721insertion1nstd166human GRCh37.p13 chr6: 52,943,256-52,943,256 , GRCh38.p12 chr6: 53,078,458-53,078,458 FBXO9
    nsv4494086mobile element insertion1nstd166human GRCh37.p13 chr6: 52,952,539-52,952,539 , GRCh38.p12 chr6: 53,087,741-53,087,741 FBXO9
    nsv4490014mobile element insertion1nstd166human GRCh37.p13 chr6: 52,962,257-52,962,257 , GRCh38.p12 chr6: 53,097,459-53,097,459 FBXO9
    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
    nsv4144863copy number variation1nstd166human GRCh37.p13 chr6: 52,955,179-52,955,304 , GRCh38.p12 chr6: 53,090,381-53,090,506 FBXO9, RN7SL244P
    nsv4139171copy number variation1nstd166human GRCh37.p13 chr6: 52,952,830-52,954,663 , GRCh38.p12 chr6: 53,088,032-53,089,865 FBXO9, RN7SL244P
    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
    nsv3922315copy number variation1nstd102humanPathogenic GRCh37 chr6: 50,938,895-57,297,586 , NCBI36 chr6: 51,046,854-57,405,545 , GRCh38 chr6: 50,971,182-57,432,788 MLIP-AS1, GSTA9P, 100 more genes
    nsv3910455copy number variation1nstd102humanPathogenic GRCh37 chr6: 51,061,467-53,724,432 , GRCh38 chr6: 51,093,754-53,859,634 , NCBI36 chr6: 51,169,426-53,832,391 LOC101927082, FBXO9, 58 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 ITPR3, HSD17B8, 2905 more genes
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