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Items: 1 to 20 of 179

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980377copy number variation1nstd102humanUncertain significance GRCh37 chr6: 31,827,495-31,830,553 , GRCh38.p12 chr6: 31,859,718-31,862,776 NEU1, SLC44A4
    nsv5541311insertion1nstd206human GRCh38 chr6: 31,874,129-31,874,163 , GRCh37.p13 chr6: 31,841,906-31,841,940 SLC44A4
    nsv5234405copy number variation1nstd204human GRCh38.p13 chr6: 30,240,001-32,313,700 , GRCh37.p13 chr6: 30,207,778-32,281,477 DDAH2, LOC105375018, 175 more genes
    nsv5229879copy number variation1nstd204human GRCh38.p13 chr6: 31,502,001-32,151,900 , GRCh37.p13 chr6: 31,469,778-32,119,677 LTB, PPT2, 80 more genes
    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
    nsv4707238copy number variation1nstd195human GRCh38.p12 chr6: 31,855,324-31,931,374 , GRCh37 chr6: 31,823,101-31,899,151 C2, NEU1, 4 more genes
    nsv4683984copy number variation1nstd102humanPathogenic GRCh37 chr6: 31,824,828-31,834,398 , GRCh38.p12 chr6: 31,857,051-31,866,621 SLC44A4, NEU1
    nsv4675941copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 31,036,397-34,088,832 , GRCh38.p12 chr6: 31,068,620-34,121,055 AGER, AIF1, 217 more genes
    nsv4663676copy number variation1nstd186human GRCh37 chr6: 31,832,601-31,832,646 , GRCh38.p12 chr6: 31,864,824-31,864,869 SLC44A4
    nsv4593507copy number variation1nstd183human GRCh37 chr6: 31,838,369-31,838,477 , GRCh38.p12 chr6: 31,870,592-31,870,700 SLC44A4
    nsv4592288copy number variation1nstd183human GRCh37 chr6: 31,832,601-31,832,700 , GRCh38.p12 chr6: 31,864,824-31,864,923 SLC44A4
    nsv4592287copy number variation1nstd183human GRCh37 chr6: 31,832,601-31,832,646 , GRCh38.p12 chr6: 31,864,824-31,864,869 SLC44A4
    nsv4350067copy number variation1nstd102humanPathogenic GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650 HLA-DPB2, CIMIP3, 1001 more genes
    nsv3965549copy number variation1nstd168human GRCh38 chr6: 31,873,665-31,915,876 , GRCh37.p13 chr6: 31,841,442-31,883,653 ZBTB12, EHMT2, 3 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
    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
    nsv3887325copy number variation1nstd102humanLikely benign GRCh37 chr6: 31,777,500-31,831,302 , GRCh38.p12 chr6: 31,809,723-31,863,525 HSPA1A, HSPA1B, 6 more genes
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