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Items: 1 to 20 of 104

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6795846copy number variation1nstd229human GRCh38 chr6: 50,041,120-50,119,225 , GRCh37.p13 chr6: 50,008,833-50,086,938 LOC100505985, DEFB112
    nsv6788988copy number variation1nstd229human GRCh38 chr6: 49,959,907-50,381,479 , GRCh37.p13 chr6: 49,927,620-50,349,192 LOC100505985, DEFB112, 3 more genes
    nsv6314749copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 43,636,308-64,947,206 , GRCh38.p12 chr6: 43,668,571-64,237,313 ACTG1P9, CRISP1, 245 more genes
    nsv6312581copy number variation1nstd102humanPathogenic GRCh37 chr6: 50,011,288-50,812,180 , GRCh38.p12 chr6: 50,043,575-50,844,467 TFAP2D, LOC100505985, 3 more genes
    nsv6136509copy number variation1nstd213human GRCh37 chr6: 50,020,000-50,080,001 , GRCh38.p12 chr6: 50,052,287-50,112,288 LOC100505985
    nsv6135921copy number variation1nstd213human GRCh37 chr6: 34,700,000-52,650,001 , GRCh38.p12 chr6: 34,732,223-52,785,203 ACTG1P9, CRISP1, 361 more genes
    nsv5684161mobile element insertion1nstd211human GRCh38 chr6: 50,093,636-50,093,636 , GRCh37.p13 chr6: 50,061,349-50,061,349 LOC100505985
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5397574mobile element insertion1nstd206human GRCh38 chr6: 50,093,636-50,093,687 , GRCh37.p13 chr6: 50,061,349-50,061,400 LOC100505985
    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
    nsv4483893mobile element insertion1nstd166human GRCh37.p13 chr6: 50,062,934-50,062,934 , GRCh38.p12 chr6: 50,095,221-50,095,221 LOC100505985
    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
    nsv4146541copy number variation1nstd166human GRCh37.p13 chr6: 50,043,261-50,059,261 , GRCh38.p12 chr6: 50,075,548-50,091,548 LOC100505985
    nsv4143489copy number variation1nstd166human GRCh37.p13 chr6: 50,025,869-50,070,701 , GRCh38.p12 chr6: 50,058,156-50,102,988 LOC100505985
    nsv4136589copy number variation1nstd166human GRCh37.p13 chr6: 50,066,806-50,066,856 , GRCh38.p12 chr6: 50,099,093-50,099,143 LOC100505985
    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
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