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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
    nsv5473625copy number variation1nstd206human GRCh38 chr6: 49,690,434-49,880,145 , GRCh37.p13 chr6: 49,658,147-49,847,858 CRISP1, PGK2, 4 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
    nsv4480349mobile element insertion1nstd166human GRCh37.p13 chr6: 49,752,262-49,752,262 , GRCh38.p12 chr6: 49,784,549-49,784,549 PGK2
    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
    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
    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
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 ITPR3, HSD17B8, 2905 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 SOD1P1, HLA-DPB1, 2905 more genes
    nsv3884243copy number variation1nstd102humanPathogenic GRCh37 chr6: 43,636,308-50,947,320 , GRCh38.p12 chr6: 43,668,571-50,979,607 GLYATL3, RNU6-754P, 105 more genes
    nsv3880081copy number variation1nstd102humanUncertain significance GRCh37 chr6: 48,682,849-49,834,213 , GRCh38.p12 chr6: 48,715,217-49,866,500 CRISP1, CRISP2, 14 more genes
    nsv3879811copy number variation1nstd102humanPathogenic GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083 RNU6-411P, LOC107986611, 2910 more genes
    nsv3877040copy number variation1nstd102humanPathogenic GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698 LOC105378061, MIR4640, 2914 more genes
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