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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
    nsv5903214copy number variation1nstd209human GRCh38 chr6: 41,904,100-41,904,289 , GRCh37.p13 chr6: 41,871,838-41,872,027 MED20
    nsv5845607copy number variation1nstd209human GRCh38 chr6: 41,910,256-41,912,009 , GRCh37.p13 chr6: 41,877,994-41,879,747 MED20
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5115957mobile element insertion1nstd203human GRCh38 chr6: 41,918,541-41,918,578 , GRCh37.p13 chr6: 41,886,279-41,886,316 MED20
    nsv5111430mobile element insertion1nstd203human GRCh38 chr6: 41,918,969-41,918,991 , GRCh37.p13 chr6: 41,886,707-41,886,729 MED20
    nsv5104865mobile element insertion1nstd203human GRCh38 chr6: 41,918,663-41,918,681 , GRCh37.p13 chr6: 41,886,401-41,886,419 MED20
    nsv4816162copy number variation1nstd200human GRCh37 chr6: 41,882,915-41,883,085 , GRCh38.p12 chr6: 41,915,177-41,915,347 MED20
    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
    nsv4592651copy number variation1nstd183human GRCh37 chr6: 41,758,583-41,983,007 , GRCh38.p12 chr6: 41,790,845-42,015,269 , BYSL, 4 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
    nsv4135005copy number variation1nstd166human GRCh37.p13 chr6: 41,877,798-41,877,850 , GRCh38.p12 chr6: 41,910,060-41,910,112 MED20
    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
    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
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