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Items: 1 to 20 of 108

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6789968copy number variation1nstd229human GRCh38 chr6: 49,738,400-49,857,157 , GRCh37.p13 chr6: 49,706,113-49,824,870 LOC101927020, CRISP1, 3 more genes
    nsv6789367copy number variation1nstd229human GRCh38 chr6: 48,645,525-49,878,656 , GRCh37.p13 chr6: 48,613,261-49,846,369 LOC100421158, CYP2AC1P, 14 more genes
    nsv6404761copy number variation1nstd223human GRCh38 chr6: 49,785,845-49,786,558 , GRCh37.p13 chr6: 49,753,558-49,754,271 PGK2
    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
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5473625copy number variation1nstd206human GRCh38 chr6: 49,690,434-49,880,145 , GRCh37.p13 chr6: 49,658,147-49,847,858 CRISP1, PGK2, 4 more genes
    nsv5040265inversion1nstd200human GRCh38 chr6: 49,481,877-49,812,356 , GRCh37.p13 chr6: 49,449,590-49,780,069 PGK2, RHAG, 7 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
    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
    nsv4480349mobile element insertion1nstd166human GRCh37.p13 chr6: 49,752,262-49,752,262 , GRCh38.p12 chr6: 49,784,549-49,784,549 PGK2
    nsv4456000copy number variation1nstd102humanUncertain significance GRCh37 chr6: 48,617,762-49,836,065 , GRCh38.p12 chr6: 48,650,026-49,868,352 LOC100421158, EEF1A1P42, 14 more genes
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