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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5963625insertion1nstd209human GRCh38 chr6: 37,090,251-37,090,251 , GRCh37.p13 chr6: 37,058,027-37,058,027 RPL12P2
    nsv5676048mobile element insertion1nstd211human GRCh38 chr6: 37,090,272-37,090,272 , GRCh37.p13 chr6: 37,058,048-37,058,048 RPL12P2
    nsv5200371copy number variation1nstd102humanPathogenic GRCh37 chr6: 34,401,304-38,435,497 , GRCh38.p12 chr6: 34,433,527-38,467,721 RPS15AP19, FKBP5, 95 more genes
    nsv5114857mobile element insertion1nstd203human GRCh38 chr6: 37,089,827-37,089,842 , GRCh37.p13 chr6: 37,057,603-37,057,618 RPL12P2
    nsv5107584mobile element insertion1nstd203human GRCh38 chr6: 37,090,251-37,090,272 , GRCh37.p13 chr6: 37,058,027-37,058,048 RPL12P2
    nsv5031134inversion1nstd200human GRCh38 chr6: 35,178,266-40,407,996 , GRCh37.p13 chr6: 35,146,043-40,375,735 , LOC105375040, 114 more genes
    nsv4940935copy number variation1nstd200human GRCh38 chr6: 37,084,347-37,090,569 , GRCh37.p13 chr6: 37,052,123-37,058,345 RPL12P2
    nsv4934637copy number variation1nstd200human GRCh38 chr6: 36,809,158-37,140,216 , GRCh37.p13 chr6: 36,776,934-37,107,992 C6orf89, MTCH1, 6 more genes
    nsv4872414inversion1nstd200human GRCh37 chr6: 35,146,053-40,375,735 , GRCh38.p12 chr6: 35,178,276-40,407,996 , RPL36P9, 114 more genes
    nsv4816050copy number variation1nstd200human GRCh37 chr6: 37,052,123-37,058,345 , GRCh38.p12 chr6: 37,084,347-37,090,569 RPL12P2
    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
    nsv4494333mobile element insertion1nstd166human GRCh37.p13 chr6: 37,059,723-37,059,723 , GRCh38.p12 chr6: 37,091,947-37,091,947 RPL12P2
    nsv4455569copy number variation1nstd102humanUncertain significance GRCh37 chr6: 36,776,798-37,106,051 , GRCh38.p12 chr6: 36,809,022-37,138,275 PI16, MTCH1, 6 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
    nsv4122663copy number variation1nstd166human GRCh37.p13 chr6: 37,034,897-37,059,893 , GRCh38.p12 chr6: 37,067,121-37,092,117 RPL12P2
    nsv3914250copy number variation1nstd102humanLikely pathogenic GRCh38 chr6: 36,822,889-37,159,699 , NCBI36 chr6: 36,898,643-37,235,453 , GRCh37 chr6: 36,790,665-37,127,475 MTCH1, PPIL1, 6 more genes
    nsv3913920copy number variation1nstd102humanPathogenic GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028 TRR-ACG1-2, TMEM217, 1385 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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