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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5960152insertion1nstd209human GRCh38 chr6: 54,772,397-54,772,397 , GRCh37.p13 chr6: 54,637,195-54,637,195 LOC107986606, KRASP1
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 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
    nsv4487331mobile element insertion1nstd166human GRCh37.p13 chr6: 54,640,368-54,640,368 , GRCh38.p12 chr6: 54,775,570-54,775,570 LOC107986606, KRASP1
    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
    nsv4140481copy number variation1nstd166human GRCh37.p13 chr6: 54,582,892-54,666,070 , GRCh38.p12 chr6: 54,718,094-54,801,272 KRASP1, RNU6-1023P, 1 more genes
    nsv3958544copy number variation1nstd168human GRCh38 chr6: 54,750,802-54,858,124 , GRCh37.p13 chr6: 54,615,600-54,722,922 KRASP1, LOC107986606, 2 more genes
    nsv3923753copy number variation1nstd102humanPathogenic GRCh38 chr6: 54,263,893-56,826,637 , GRCh37 chr6: 54,128,691-56,691,435 , NCBI36 chr6: 54,236,650-56,799,394 RNU6-1023P, MLIP, 20 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
    nsv3915840copy number variation1nstd102humanPathogenic GRCh38 chr6: 53,931,543-68,149,750 , GRCh37 chr6: 53,796,341-68,859,642 , NCBI36 chr6: 53,904,300-68,916,363 LOC442225, RAB23, 104 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
    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
    nsv3874732copy number variation1nstd102humanUncertain significance GRCh37 chr6: 53,661,282-55,147,137 , GRCh38.p12 chr6: 53,796,484-55,282,339 RNU6-1023P, LOC107986606, 16 more genes
    esv4011098complex chromosomal rearrangement4estd236human GRCh37 chr6: 48,385,249-154,434,404 , GRCh38.p12 chr6: 48,417,513-154,113,269 , ACTBP8, 1274 more genes
    nsv3169066inversion1nstd158human GRCh37 chr6: 5,923,377-99,717,885 , GRCh38.p12 chr6: 5,923,144-99,270,009 , ABCF1, 1877 more genes
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