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Items: 1 to 20 of 257

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5466688copy number variation1nstd206human GRCh38 chr6: 11,775,127-11,775,199 , GRCh37.p13 chr6: 11,775,360-11,775,432 ADTRP
    nsv5162566mobile element insertion1nstd203human GRCh38 chr6: 11,752,224-11,752,236 , GRCh37.p13 chr6: 11,752,457-11,752,469 ADTRP
    nsv5090618mobile element insertion1nstd203human GRCh38 chr6: 11,734,294-11,734,307 , GRCh37.p13 chr6: 11,734,527-11,734,540 ADTRP
    nsv4934387copy number variation1nstd200human GRCh38 chr6: 7,366,072-12,459,747 , GRCh37.p13 chr6: 7,366,305-12,459,979 , DSP, 90 more genes
    nsv4932729copy number variation1nstd200human GRCh38 chr6: 11,760,226-11,761,290 , GRCh37.p13 chr6: 11,760,459-11,761,523 ADTRP
    nsv4932728copy number variation1nstd200human GRCh38 chr6: 11,720,913-11,724,904 , GRCh37.p13 chr6: 11,721,146-11,725,137 , 1 more genes
    nsv4932727copy number variation1nstd200human GRCh38 chr6: 11,712,054-11,723,859 , GRCh37.p13 chr6: 11,712,287-11,724,092 , ADTRP
    nsv4932725copy number variation1nstd200human GRCh38 chr6: 11,675,030-11,729,568 , GRCh37.p13 chr6: 11,675,263-11,729,801 , 2 more genes
    nsv4809729copy number variation1nstd200human GRCh37 chr6: 11,712,287-11,724,092 , GRCh38.p12 chr6: 11,712,054-11,723,859 , ADTRP
    nsv4809727copy number variation1nstd200human GRCh37 chr6: 11,675,262-11,729,801 , GRCh38.p12 chr6: 11,675,029-11,729,568 , 2 more genes
    nsv4497146mobile element insertion1nstd166human GRCh37.p13 chr6: 11,741,630-11,741,630 , GRCh38.p12 chr6: 11,741,397-11,741,397 ADTRP
    nsv4492527mobile element insertion1nstd166human GRCh37.p13 chr6: 11,740,105-11,740,105 , GRCh38.p12 chr6: 11,739,872-11,739,872 ADTRP
    nsv4456780copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-23,221,621 , GRCh38.p12 chr6: 156,974-23,221,393 LOC105374960, LOC101928573, 342 more genes
    nsv4324882inversion1nstd166human GRCh37.p13 chr6: 11,087,007-14,472,606 , GRCh38.p12 chr6: 11,086,774-14,472,375 , HIVEP1, 56 more genes
    nsv4114928copy number variation1nstd166human GRCh37.p13 chr6: 11,675,263-11,729,807 , GRCh38.p12 chr6: 11,675,030-11,729,574 , 2 more genes
    nsv3922052copy number variation1nstd102humanPathogenic GRCh37 chr6: 155,807-17,058,645 , NCBI36 chr6: 100,807-17,166,624 , GRCh38 chr6: 155,807-17,058,414 ECI2-DT, RNU1-11P, 268 more genes
    nsv3921817copy number variation1nstd102humanPathogenic GRCh37 chr6: 2,862,874-16,698,019 , GRCh38 chr6: 2,862,640-16,697,788 , NCBI36 chr6: 2,807,873-16,805,998 RN7SKP293, LOC105374906, 230 more genes
    nsv3921027copy number variation1nstd102humanPathogenic GRCh38 chr6: 389,423-13,474,956 , GRCh37 chr6: 389,423-13,475,188 , NCBI36 chr6: 334,423-13,583,167 LOC105374898, HIVEP1, 215 more genes
    nsv3920564copy number variation1nstd102humanPathogenic GRCh38 chr6: 3,224,310-30,657,190 , GRCh37 chr6: 3,224,544-30,624,967 , NCBI36 chr6: 3,169,543-30,732,946 PRELID1P2, RPL7AP7, 785 more genes
    nsv3918220copy number variation1nstd102humanPathogenic GRCh38 chr6: 10,601,499-13,987,316 , NCBI36 chr6: 10,709,718-14,095,526 , GRCh37 chr6: 10,601,732-13,987,547 GCNT2, LOC105374935, 58 more genes
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