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Items: 1 to 20 of 121

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097826copy number variation1nstd102humanPathogenic GRCh37 chr6: 41,126,341-43,752,536 , GRCh38.p12 chr6: 41,158,603-43,784,799 USP49, PRICKLE4, 96 more genes
    nsv7097825copy number variation1nstd102humanUncertain significance GRCh37 chr6: 41,126,341-43,737,486 , GRCh38.p12 chr6: 41,158,603-43,769,749 DNPH1, LOC107986596, 96 more genes
    nsv7043293inversion1nstd229human GRCh38 chr6: 39,854,165-43,261,822 , GRCh37.p13 chr6: 39,821,941-43,229,560 RPL23P6, RPL32P15, 95 more genes
    nsv6781081copy number variation1nstd229human GRCh38 chr6: 41,233,249-41,234,096 , GRCh37.p13 chr6: 41,200,987-41,201,834 TREML4
    nsv6779187copy number variation1nstd229human GRCh38 chr6: 41,238,775-41,243,519 , GRCh37.p13 chr6: 41,206,513-41,211,257 TREML4, RNA5SP207
    nsv6564334inversion1nstd223human GRCh38 chr6: 41,198,166-41,249,567 , GRCh37.p13 chr6: 41,165,904-41,217,305 TREML2, TREML5P, 4 more genes
    nsv6559522inversion1nstd223human GRCh38 chr6: 41,231,050-41,232,586 , GRCh37.p13 chr6: 41,198,788-41,200,324 TREML4
    nsv6398378copy number variation1nstd223human GRCh38 chr6: 41,233,001-41,234,500 , GRCh37.p13 chr6: 41,200,739-41,202,238 TREML4
    nsv6147085inversion1nstd206human GRCh38 chr6: 41,197,504-41,250,183 , GRCh37.p13 chr6: 41,165,242-41,217,921 TREML2, TREML5P, 4 more genes
    nsv6135921copy number variation1nstd213human GRCh37 chr6: 34,700,000-52,650,001 , GRCh38.p12 chr6: 34,732,223-52,785,203 ACTG1P9, CRISP1, 361 more genes
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 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
    nsv4675176copy number variation1nstd102humanUncertain significance GRCh37 chr6: 41,200,840-41,331,797 , GRCh38.p12 chr6: 41,233,102-41,364,059 NCR2, RPL32P15, 5 more genes
    nsv4598583copy number variation1nstd183human GRCh37 chr6: 41,204,150-41,204,341 , GRCh38.p12 chr6: 41,236,412-41,236,603 TREML4
    nsv4564191mobile element insertion1nstd166human GRCh37.p13 chr6: 41,205,402-41,205,402 , GRCh38.p12 chr6: 41,237,664-41,237,664 TREML4, RNA5SP207
    nsv4555799insertion1nstd166human GRCh37.p13 chr6: 41,203,618-41,203,618 , GRCh38.p12 chr6: 41,235,880-41,235,880 TREML4
    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
    nsv3919521copy number variation1nstd102humanPathogenic NCBI36 chr6: 37,853,123-45,729,558 , GRCh37 chr6: 37,745,145-45,621,580 , GRCh38 chr6: 37,777,369-45,653,843 RPL23P6, LOC102723789, 184 more genes
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