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Items: 1 to 20 of 199

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5892330copy number variation1nstd209human GRCh38 chr6: 35,948,470-36,584,214 , GRCh37.p13 chr6: 35,916,247-36,551,991 SLC26A8, STK38, 17 more genes
    nsv5729158mobile element insertion1nstd211human GRCh38 chr6: 36,474,831-36,474,831 , GRCh37.p13 chr6: 36,442,608-36,442,608 KCTD20
    nsv5679594mobile element insertion1nstd211human GRCh38 chr6: 36,480,433-36,480,433 , GRCh37.p13 chr6: 36,448,210-36,448,210 KCTD20
    nsv5462334copy number variation1nstd206human GRCh38 chr6: 36,473,286-36,473,339 , GRCh37.p13 chr6: 36,441,063-36,441,116 KCTD20
    nsv5459386copy number variation1nstd206human GRCh38 chr6: 36,480,585-36,485,612 , GRCh37.p13 chr6: 36,448,362-36,453,389 KCTD20
    nsv5458580copy number variation1nstd206human GRCh38 chr6: 36,462,828-36,467,454 , GRCh37.p13 chr6: 36,430,605-36,435,231 KCTD20
    nsv5200371copy number variation1nstd102humanPathogenic GRCh37 chr6: 34,401,304-38,435,497 , GRCh38.p12 chr6: 34,433,527-38,467,721 RPS15AP19, FKBP5, 95 more genes
    nsv5104521mobile element insertion1nstd203human GRCh38 chr6: 36,453,524-36,453,553 , GRCh37.p13 chr6: 36,421,301-36,421,330 KCTD20
    nsv5031134inversion1nstd200human GRCh38 chr6: 35,178,266-40,407,996 , GRCh37.p13 chr6: 35,146,043-40,375,735 , LOC105375040, 114 more genes
    nsv4940898copy number variation1nstd200human GRCh38 chr6: 36,484,371-36,487,038 , GRCh37.p13 chr6: 36,452,148-36,454,815 KCTD20
    nsv4940897copy number variation1nstd200human GRCh38 chr6: 36,473,357-36,485,702 , GRCh37.p13 chr6: 36,441,134-36,453,479 KCTD20
    nsv4940896copy number variation1nstd200human GRCh38 chr6: 36,471,570-36,473,732 , GRCh37.p13 chr6: 36,439,347-36,441,509 KCTD20
    nsv4940895copy number variation1nstd200human GRCh38 chr6: 36,471,120-36,482,470 , GRCh37.p13 chr6: 36,438,897-36,450,247 KCTD20
    nsv4940894copy number variation1nstd200human GRCh38 chr6: 36,445,772-36,446,616 , GRCh37.p13 chr6: 36,413,549-36,414,393 KCTD20
    nsv4940893copy number variation1nstd200human GRCh38 chr6: 36,443,191-36,443,362 , GRCh37.p13 chr6: 36,410,968-36,411,139 PXT1, KCTD20
    nsv4934635copy number variation1nstd200human GRCh38 chr6: 36,482,282-36,482,714 , GRCh37.p13 chr6: 36,450,059-36,450,491 KCTD20
    nsv4934634copy number variation1nstd200human GRCh38 chr6: 36,479,699-36,480,687 , GRCh37.p13 chr6: 36,447,476-36,448,464 KCTD20
    nsv4934632copy number variation1nstd200human GRCh38 chr6: 36,405,862-36,962,727 , GRCh37.p13 chr6: 36,373,639-36,930,503 RN7SL502P, PPIL1, 17 more genes
    nsv4872414inversion1nstd200human GRCh37 chr6: 35,146,053-40,375,735 , GRCh38.p12 chr6: 35,178,276-40,407,996 , RPL36P9, 114 more genes
    nsv4828643copy number variation1nstd200human GRCh37 chr6: 36,448,310-36,453,414 , GRCh38.p12 chr6: 36,480,533-36,485,637 KCTD20
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