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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
    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
    nsv4498024mobile element insertion1nstd166human GRCh37.p13 chr6: 56,809,354-56,809,354 , GRCh38.p12 chr6: 56,944,556-56,944,556 RNU6-626P, DST
    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
    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
    nsv3920671copy number variation1nstd102humanUncertain significance GRCh38 chr6: 56,639,682-57,432,788 , NCBI36 chr6: 56,612,439-57,405,545 , GRCh37 chr6: 56,504,480-57,297,586 OSTCP6, MIR548U, 14 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
    nsv3912575copy number variation1nstd102humanUncertain significance GRCh37 chr6: 56,177,722-57,171,010 , NCBI36 chr6: 56,285,681-57,278,969 , GRCh38 chr6: 56,312,924-57,306,212 KIAA1586, LINC03001, 14 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
    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
    nsv3168939inversion1nstd158human GRCh37 chr6: 12,268,690-80,058,596 , GRCh38.p12 chr6: 12,268,457-79,348,879 , ABCF1, 1548 more genes
    nsv3168805inversion1nstd158human GRCh37 chr6: 12,296,990-80,059,394 , GRCh38.p12 chr6: 12,296,757-79,349,677 , ABCF1, 1548 more genes
    nsv3168551inversion1nstd158human GRCh37 chr6: 7,798,260-81,124,626 , GRCh38.p12 chr6: 7,798,027-80,414,909 , ABCF1, 1644 more genes
    nsv3168209copy number variation1nstd158human GRCh38.p12 chr6: 56,099,235-128,190,528 , GRCh37 chr6: 55,964,033-128,511,673 , ACTBP8, 798 more genes
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