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Items: 1 to 20 of 153

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5234405copy number variation1nstd204human GRCh38.p13 chr6: 30,240,001-32,313,700 , GRCh37.p13 chr6: 30,207,778-32,281,477 DDAH2, LOC105375018, 175 more genes
    nsv5229879copy number variation1nstd204human GRCh38.p13 chr6: 31,502,001-32,151,900 , GRCh37.p13 chr6: 31,469,778-32,119,677 LTB, PPT2, 80 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
    nsv4675941copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 31,036,397-34,088,832 , GRCh38.p12 chr6: 31,068,620-34,121,055 AGER, AIF1, 217 more genes
    nsv4675453copy number variation1nstd102humanUncertain significance GRCh37 chr6: 31,916,915-32,278,000 , GRCh38.p12 chr6: 31,949,138-32,310,223 NOTCH4, CYP21A2, 29 more genes
    nsv4455450copy number variation1nstd102humanUncertain significance GRCh37 chr6: 32,027,371-32,448,599 , GRCh38.p12 chr6: 32,059,594-32,480,822 AGPAT1, HCG23, 23 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
    nsv3955465copy number variation1nstd168human GRCh38 chr6: 32,116,333-32,129,069 , GRCh37.p13 chr6: 32,084,110-32,096,846 ATF6B, FKBPL
    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
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 SOD1P1, HLA-DPB1, 2905 more genes
    nsv3886007copy number variation1nstd102humanUncertain significance GRCh37 chr6: 31,952,482-32,243,155 , GRCh38.p12 chr6: 31,984,705-32,275,378 STK19B, NOTCH4, 22 more genes
    nsv3884305copy number variation1nstd102humanUncertain significance GRCh37 chr6: 32,052,479-32,184,403 , GRCh38.p12 chr6: 32,084,702-32,216,626 PRRT1, PPT2-EGFL8, 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
    nsv3877326copy number variation1nstd102humanLikely benign GRCh37 chr6: 32,088,893-32,098,036 , GRCh38.p12 chr6: 32,121,116-32,130,259 ATF6B, FKBPL
    nsv3877040copy number variation1nstd102humanPathogenic GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698 LOC105378061, MIR4640, 2914 more genes
    nsv3870570copy number variation1nstd102humanUncertain significance GRCh37 chr6: 28,130,359-32,108,367 , GRCh38.p12 chr6: 28,162,581-32,140,590 LOC105375002, SKIC2, 345 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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