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Items: 1 to 20 of 169

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5378353translocation1nstd200human GRCh38 chr7: 80,713,087-80,713,087 , GRCh38 chr6: 31,809,780-31,809,780 , GRCh37.p13 chr6: 31,777,557-31,777,557 , GRCh37.p13 chr7: 80,342,403-80,342,403 HSPA1L
    nsv5301808copy number variation1nstd204human GRCh37.p13 chr6: 31,776,329-31,804,587 , GRCh38.p13 chr6: 31,808,552-31,836,810 HSPA1A, HSPA1B, 4 more genes
    nsv5235511copy number variation1nstd204human GRCh38.p13 chr6: 31,808,301-31,834,300 , GRCh37.p13 chr6: 31,776,078-31,802,077 HSPA1B, SNORD48, 3 more genes
    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
    nsv5229526copy number variation1nstd204human GRCh38.p13 chr6: 31,620,501-31,855,300 , GRCh37.p13 chr6: 31,588,278-31,823,077 LOC105375018, DDAH2, 35 more genes
    nsv5221581copy number variation1nstd204human GRCh38.p13 chr6: 31,814,734-31,827,310 , GRCh37.p13 chr6: 31,782,511-31,795,087 HSPA1B, HSPA1L, 1 more genes
    nsv5100384mobile element insertion1nstd203human GRCh38 chr6: 31,809,722-31,809,740 , GRCh37.p13 chr6: 31,777,499-31,777,517 HSPA1L
    nsv4934581copy number variation1nstd200human GRCh38 chr6: 31,812,205-31,813,447 , GRCh37.p13 chr6: 31,779,982-31,781,224 HSPA1L
    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
    nsv4706993copy number variation1nstd195human GRCh37 chr6: 31,587,351-31,783,751 , GRCh38.p12 chr6: 31,619,574-31,815,974 BAG6, ABHD16A, 31 more genes
    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
    nsv4593505copy number variation2nstd183human GRCh37 chr6: 31,783,557-31,801,820 , GRCh38.p12 chr6: 31,815,780-31,834,043 HSPA1A, SNORD48, 3 more genes
    nsv4394176copy number variation1nstd174human GRCh37 chr6: 31,782,617-31,797,587 , GRCh38.p12 chr6: 31,814,840-31,829,810 HSPA1B, HSPA1A, 1 more genes
    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
    nsv3961161copy number variation1nstd168human GRCh38 chr6: 31,815,681-31,829,597 , GRCh37.p13 chr6: 31,783,458-31,797,374 HSPA1B, HSPA1A, 1 more genes
    nsv3958606insertion1nstd168human GRCh38 chr6: 31,776,597-31,822,496 , GRCh37.p13 chr6: 31,744,374-31,790,273 HSPA1A, HSPA1L, 3 more genes
    nsv3921657copy number variation1nstd102humanUncertain significance NCBI36 chr6: 31,773,217-31,934,913 , GRCh37.p13 chr6|NT_167245.1: 2,950,808-3,112,520 , GRCh37.p13 chr6|NT_167247.1: 3,044,917-3,154,498 , GRCh37.p13 chr6|NT_167249.1: 3,054,967-3,159,682 , GRCh37.p13 chr6|NT_167244.1: 3,037,483-3,141,689 , GRCh37.p13 chr6: 31,665,238-31,826,934 , GRCh38.p12 chr6: 31,697,461-31,859,157 , GRCh38.p12 chr6|NT_167247.2: 3,039,332-3,148,913 , GRCh38.p12 chr6|NT_167249.2: 3,055,670-3,160,384 , GRCh38.p12 chr6|NT_167245.2: 2,945,223-3,106,935 , GRCh38.p12 chr6|NT_167244.2: 3,087,568-3,191,773 CLIC1, SAPCD1, 24 more genes
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