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Items: 1 to 20 of 143

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5087217mobile element insertion1nstd203human GRCh38 chr6: 11,700,585-11,700,601 , GRCh37.p13 chr6: 11,700,818-11,700,834 LOC340184
    nsv4934387copy number variation1nstd200human GRCh38 chr6: 7,366,072-12,459,747 , GRCh37.p13 chr6: 7,366,305-12,459,979 , DSP, 90 more genes
    nsv4932725copy number variation1nstd200human GRCh38 chr6: 11,675,030-11,729,568 , GRCh37.p13 chr6: 11,675,263-11,729,801 , 2 more genes
    nsv4809727copy number variation1nstd200human GRCh37 chr6: 11,675,262-11,729,801 , GRCh38.p12 chr6: 11,675,029-11,729,568 , 2 more genes
    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
    nsv4129997copy number variation1nstd166human GRCh37.p13 chr6: 11,700,660-11,700,736 , GRCh38.p12 chr6: 11,700,427-11,700,503 LOC340184
    nsv4116732copy number variation1nstd166human GRCh37.p13 chr6: 11,701,144-11,705,302 , GRCh38.p12 chr6: 11,700,911-11,705,069 LOC340184
    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
    nsv3914672copy number variation1nstd102humanLikely pathogenic NCBI36 chr6: 101,974-13,189,419 , GRCh37 chr6: 156,974-13,081,433 , GRCh38 chr6: 156,974-13,081,201 BMP6, BPHL, 212 more genes
    nsv3914068copy number variation1nstd102humanPathogenic NCBI36 chr6: 4,014,025-13,376,010 , GRCh38 chr6: 4,068,792-13,267,799 , GRCh37 chr6: 4,069,026-13,268,031 SSR1, LOC107986560, 145 more genes
    nsv3913920copy number variation1nstd102humanPathogenic GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028 TRR-ACG1-2, TMEM217, 1385 more genes
    nsv3913657copy number variation1nstd102humanPathogenic NCBI36 chr6: 51,431-18,468,805 , GRCh38 chr6: 106,431-18,360,595 , GRCh37 chr6: 106,431-18,360,826 LOC105374904, CAP2, 294 more genes
    nsv3913587copy number variation1nstd102humanPathogenic GRCh38 chr6: 152,634-14,417,003 , NCBI36 chr6: 97,634-14,525,213 , GRCh37 chr6: 152,634-14,417,234 LINC01600, LOC105374943, 236 more genes
    nsv3913192copy number variation1nstd102humanPathogenic NCBI36 chr6: 97,634-15,840,373 , GRCh37.p13 chr6: 152,634-15,732,394 , GRCh38.p12 chr6: 152,634-15,732,163 FARS2, PSMC1P11, 252 more genes
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