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Items: 1 to 20 of 215

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5959243insertion1nstd209human GRCh38 chr6: 41,738,200-41,738,200 , GRCh37.p13 chr6: 41,705,938-41,705,938 PGC
    nsv5631236insertion1nstd207human GRCh38 chr6: 41,738,241-41,738,241 , GRCh37.p13 chr6: 41,705,979-41,705,979 PGC
    nsv5626450insertion1nstd207human GRCh38 chr6: 41,738,205-41,738,205 , GRCh37.p13 chr6: 41,705,943-41,705,943 PGC
    nsv5569641copy number variation1nstd207human GRCh38 chr6: 41,738,149-41,738,250 , GRCh37.p13 chr6: 41,705,887-41,705,988 PGC
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5362893translocation1nstd200human GRCh38 chr6: 41,743,091-41,743,091 , GRCh38 chr6: 41,743,574-41,743,574 , GRCh37.p13 chr6: 41,710,829-41,710,829 , GRCh37.p13 chr6: 41,711,312-41,711,312 PGC
    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
    nsv4725656insertion1nstd186human GRCh37 chr6: 41,705,893-41,705,893 , GRCh38.p12 chr6: 41,738,155-41,738,155 PGC
    nsv4598585copy number variation1nstd183human GRCh37 chr6: 41,701,716-41,703,573 , GRCh38.p12 chr6: 41,733,978-41,735,835 TFEB, MIR10398, 1 more genes
    nsv4549286insertion1nstd166human GRCh37.p13 chr6: 41,705,893-41,705,893 , GRCh38.p12 chr6: 41,738,155-41,738,155 PGC
    nsv4411378copy number variation1nstd174human GRCh37 chr6: 41,701,674-41,703,587 , GRCh38.p12 chr6: 41,733,936-41,735,849 TFEB, PGC, 1 more genes
    nsv4393025copy number variation1nstd174human GRCh37 chr6: 41,705,633-41,706,203 , GRCh38.p12 chr6: 41,737,895-41,738,465 PGC
    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
    nsv4146434copy number variation1nstd166human GRCh37.p13 chr6: 41,705,894-41,706,671 , GRCh38.p12 chr6: 41,738,156-41,738,933 PGC
    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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