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Items: 1 to 20 of 95

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7045032inversion1nstd229human GRCh38 chr6: 49,872,474-49,959,976 , GRCh37.p13 chr6: 49,840,187-49,927,689 DEFB133, CRISP1, 1 more genes
    nsv6795271copy number variation1nstd229human GRCh38 chr6: 49,332,174-50,024,818 , GRCh37.p13 chr6: 49,299,844-49,992,531 DEFB114, LOC101927020, 16 more genes
    nsv6791174copy number variation1nstd229human GRCh38 chr6: 49,494,055-50,046,260 , GRCh37.p13 chr6: 49,461,768-50,013,973 DEFB110, CRISP1, 13 more genes
    nsv6790030copy number variation1nstd229human GRCh38 chr6: 49,948,761-49,956,592 , GRCh37.p13 chr6: 49,916,474-49,924,305 DEFB133
    nsv6570761inversion1nstd223human GRCh38 chr6: 49,949,748-49,950,383 , GRCh37.p13 chr6: 49,917,461-49,918,096 DEFB133
    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
    nsv6290935copy number variation1nstd102humanUncertain significance GRCh37 chr6: 49,459,881-50,012,992 , GRCh38.p12 chr6: 49,492,168-50,045,279 DEFB133, PGK2, 14 more genes
    nsv6136508copy number variation1nstd213human GRCh37 chr6: 49,700,000-50,020,001 , GRCh38.p12 chr6: 49,732,287-50,052,288 DEFB113, LOC101927020, 8 more genes
    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
    nsv6008838copy number variation1nstd212human GRCh38 chr6: 49,935,854-49,944,730 , GRCh37.p13 chr6: 49,903,567-49,912,443 DEFB133
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5103609mobile element insertion1nstd203human GRCh38 chr6: 49,949,799-49,949,825 , GRCh37.p13 chr6: 49,917,512-49,917,538 DEFB133
    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
    nsv4675491copy number variation1nstd102humanUncertain significance GRCh37 chr6: 49,459,881-50,024,153 , GRCh38.p12 chr6: 49,492,168-50,056,440 LOC101927048, GLYATL3, 14 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
    nsv4132623copy number variation1nstd166human GRCh37.p13 chr6: 49,903,566-49,912,443 , GRCh38.p12 chr6: 49,935,853-49,944,730 DEFB133
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