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Items: 1 to 20 of 102

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5458560copy number variation1nstd206human GRCh38 chr6: 27,033,652-27,034,163 , GRCh37.p13 chr6: 27,001,431-27,001,942 VN1R12P
    nsv5362793translocation1nstd200human GRCh38 chr6: 27,034,163-27,034,163 , GRCh38 chr6: 27,033,652-27,033,652 , GRCh37.p13 chr6: 27,001,431-27,001,431 , GRCh37.p13 chr6: 27,001,942-27,001,942 VN1R12P
    nsv5036471inversion1nstd200human GRCh38 chr6: 25,888,426-29,704,316 , GRCh37.p13 chr6: 25,888,654-29,672,093 , OR11A1, 368 more genes
    nsv4879678inversion1nstd200human GRCh37 chr6: 25,888,654-29,672,093 , GRCh38.p12 chr6: 25,888,426-29,704,316 , H1-4, 368 more genes
    nsv4815703copy number variation1nstd200human GRCh37 chr6: 27,001,431-27,001,942 , GRCh38.p12 chr6: 27,033,652-27,034,163 VN1R12P
    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
    nsv4381128copy number variation1nstd173human GRCh37 chr6: 26,941,502-27,391,254 , GRCh38.p12 chr6: 26,973,723-27,423,475 , RPL10P2, 45 more genes
    nsv4113481copy number variation1nstd166human GRCh37.p13 chr6: 27,001,230-27,001,942 , GRCh38.p12 chr6: 27,033,451-27,034,163 VN1R12P
    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
    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
    nsv3911053copy number variation1nstd102humanUncertain significance GRCh38 chr6: 26,280,579-28,727,313 , GRCh37 chr6: 26,280,807-28,695,090 , NCBI36 chr6: 26,388,786-28,803,069 GPX5, TRI-AAT9-1, 232 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 ITPR3, HSD17B8, 2905 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 SOD1P1, HLA-DPB1, 2905 more genes
    nsv3879811copy number variation1nstd102humanPathogenic GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083 RNU6-411P, LOC107986611, 2910 more genes
    nsv3877040copy number variation1nstd102humanPathogenic GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698 LOC105378061, MIR4640, 2914 more genes
    nsv3873727copy number variation1nstd102humanUncertain significance GRCh37 chr6: 26,928,203-27,344,831 , GRCh38.p12 chr6: 26,960,424-27,377,052 TRV-CAC6-1, CDCA7P1, 42 more genes
    nsv3169066inversion1nstd158human GRCh37 chr6: 5,923,377-99,717,885 , GRCh38.p12 chr6: 5,923,144-99,270,009 , ABCF1, 1877 more genes
    nsv3168939inversion1nstd158human GRCh37 chr6: 12,268,690-80,058,596 , GRCh38.p12 chr6: 12,268,457-79,348,879 , ABCF1, 1548 more genes
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