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Items: 1 to 20 of 104

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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
    nsv6398355copy number variation1nstd223human GRCh38 chr6: 41,782,061-41,782,299 , GRCh37.p13 chr6: 41,749,799-41,750,037 PRICKLE4
    nsv6245067mobile element insertion1nstd215human GRCh38 chr6: 41,787,925-41,787,925 , GRCh37.p13 chr6: 41,755,663-41,755,663 USP49, PRICKLE4, 1 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
    nsv5678353mobile element insertion1nstd211human GRCh38 chr6: 41,787,925-41,787,925 , GRCh37.p13 chr6: 41,755,663-41,755,663 USP49, PRICKLE4, 1 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
    nsv5454944copy number variation1nstd206human GRCh38 chr6: 41,782,047-41,782,408 , GRCh37.p13 chr6: 41,749,785-41,750,146 PRICKLE4
    nsv5196383mobile element insertion1nstd203human GRCh38 chr6: 41,783,429-41,783,443 , GRCh37.p13 chr6: 41,751,167-41,751,181 PRICKLE4
    nsv5116783mobile element insertion1nstd203human GRCh38 chr6: 41,787,917-41,787,925 , GRCh37.p13 chr6: 41,755,655-41,755,663 USP49, PRICKLE4, 1 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
    nsv4572200mobile element insertion1nstd166human GRCh37.p13 chr6: 41,751,167-41,751,167 , GRCh38.p12 chr6: 41,783,429-41,783,429 PRICKLE4
    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
    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
    nsv3912856copy number variation1nstd102humanPathogenic NCBI36 chr6: 41,713,777-46,588,645 , GRCh38 chr6: 41,638,061-46,512,949 , GRCh37 chr6: 41,605,799-46,480,686 PTCRA, LOC101929770, 121 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
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