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Items: 1 to 20 of 240

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093363copy number variation1nstd102humanPathogenic GRCh37 chr6: 820,000-21,700,000 , GRCh38.p12 chr6: 820,000-21,699,769 LOC101928354, CNN3P1, 321 more genes
    nsv7054247inversion1nstd229human GRCh38 chr6: 18,141,080-21,441,150 , GRCh37.p13 chr6: 18,141,311-21,441,381 TPMT, LOC105374965, 37 more genes
    nsv7051368inversion1nstd229human GRCh38 chr6: 20,052,222-24,804,874 , GRCh37.p13 chr6: 20,052,453-24,805,102 LOC102724736, LOC105374966, 51 more genes
    nsv7039826inversion1nstd229human GRCh38 chr6: 19,226,276-22,428,371 , GRCh37.p13 chr6: 19,226,507-22,428,600 RN7SKP240, LOC107986578, 32 more genes
    nsv6796691copy number variation1nstd229human GRCh38 chr6: 20,278,801-20,365,500 , GRCh37.p13 chr6: 20,279,032-20,365,731 LOC101928573
    nsv6793310copy number variation1nstd229human GRCh38 chr6: 20,247,398-20,322,640 , GRCh37.p13 chr6: 20,247,629-20,322,871 LOC101928573
    nsv6788169copy number variation1nstd229human GRCh38 chr6: 20,277,501-20,282,100 , GRCh37.p13 chr6: 20,277,732-20,282,331 LOC101928573
    nsv6782307copy number variation1nstd229human GRCh38 chr6: 20,302,539-20,308,233 , GRCh37.p13 chr6: 20,302,770-20,308,464 LOC101928573
    nsv6778953copy number variation1nstd229human GRCh38 chr6: 20,312,158-20,315,061 , GRCh37.p13 chr6: 20,312,389-20,315,292 LOC101928573
    nsv6636333copy number variation1nstd102humanPathogenic GRCh37 chr6: 12,005,630-22,849,647 , GRCh38.p12 chr6: 12,005,397-22,849,418 SOX4, MDH1P2, 136 more genes
    nsv6563122inversion1nstd223human GRCh38 chr6: 20,273,103-20,273,759 , GRCh37.p13 chr6: 20,273,334-20,273,990 LOC101928573
    nsv6563104inversion1nstd223human GRCh38 chr6: 20,052,171-24,804,275 , GRCh37.p13 chr6: 20,052,402-24,804,503 HDGFL1, LOC105374976, 51 more genes
    nsv6409637copy number variation1nstd223human GRCh38 chr6: 20,270,401-20,271,200 , GRCh37.p13 chr6: 20,270,632-20,271,431 LOC101928573
    nsv6408725copy number variation1nstd223human GRCh38 chr6: 20,277,237-20,297,350 , GRCh37.p13 chr6: 20,277,468-20,297,581 LOC101928573
    nsv6408298copy number variation1nstd223human GRCh38 chr6: 20,302,539-20,308,230 , GRCh37.p13 chr6: 20,302,770-20,308,461 LOC101928573
    nsv6397689copy number variation1nstd223human GRCh38 chr6: 20,277,470-20,282,056 , GRCh37.p13 chr6: 20,277,701-20,282,287 LOC101928573
    nsv6308816insertion1nstd186human GRCh37 chr6: 20,281,621-20,281,665 , GRCh38.p12 chr6: 20,281,390-20,281,434 LOC101928573
    nsv6260586mobile element insertion1nstd215human GRCh38 chr6: 20,283,265-20,283,265 , GRCh37.p13 chr6: 20,283,496-20,283,496 LOC101928573
    nsv6260585mobile element insertion1nstd215human GRCh38 chr6: 20,267,021-20,267,021 , GRCh37.p13 chr6: 20,267,252-20,267,252 LOC101928573
    nsv6136494copy number variation1nstd213human GRCh37 chr6: 20,180,000-20,370,001 , GRCh38.p12 chr6: 20,179,769-20,369,770 MBOAT1, LOC101928573
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