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Items: 1 to 20 of 138

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6119728copy number variation1nstd186human GRCh37 chr6: 44,264,681-44,264,732 , GRCh38.p12 chr6: 44,296,944-44,296,995 TCTE1, AARS2
    nsv5948897insertion1nstd209human GRCh38 chr6: 44,296,935-44,296,935 , GRCh37.p13 chr6: 44,264,672-44,264,672 AARS2, TCTE1
    nsv5642251insertion1nstd207human GRCh38 chr6: 44,296,939-44,296,939 , GRCh37.p13 chr6: 44,264,676-44,264,676 AARS2, TCTE1
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5456570copy number variation1nstd206human GRCh38 chr6: 44,296,944-44,296,995 , GRCh37.p13 chr6: 44,264,681-44,264,732 TCTE1, AARS2
    nsv4934690copy number variation1nstd200human GRCh38 chr6: 44,278,416-44,278,615 , GRCh37.p13 chr6: 44,246,153-44,246,352 TCTE1, TMEM151B
    nsv4816219copy number variation1nstd200human GRCh37 chr6: 44,253,068-44,253,772 , GRCh38.p12 chr6: 44,285,331-44,286,035 TCTE1
    nsv4763773insertion1nstd199human GRCh37 chr6: 44,264,671-44,264,671 , GRCh38.p12 chr6: 44,296,934-44,296,934 AARS2, TCTE1
    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
    nsv4439789insertion1nstd175human GRCh37 chr6: 44,264,678-44,264,678 , GRCh38.p12 chr6: 44,296,941-44,296,941 AARS2, TCTE1
    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
    nsv4132930copy number variation1nstd166human GRCh37.p13 chr6: 44,250,600-44,268,000 , GRCh38.p12 chr6: 44,282,863-44,300,263 AARS2, TCTE1
    nsv3955959copy number variation1nstd168human GRCh38 chr6: 44,256,360-44,310,256 , GRCh37.p13 chr6: 44,224,097-44,277,993 SLC35B2, TMEM151B, 3 more genes
    nsv3954504copy number variation1nstd167human GRCh37 chr6: 44,264,373-44,264,403 , GRCh38.p12 chr6: 44,296,636-44,296,666 AARS2, TCTE1
    nsv3944594insertion1nstd167human GRCh37 chr6: 44,264,671-44,264,671 , GRCh38.p12 chr6: 44,296,934-44,296,934 AARS2, TCTE1
    nsv3924318copy number variation1nstd102humanPathogenic GRCh37 chr6: 42,336,296-44,558,281 , NCBI36 chr6: 42,444,274-44,666,259 , GRCh38 chr6: 42,368,558-44,590,544 MIR4642, SRF, 82 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
    nsv3919402copy number variation1nstd102humanPathogenic NCBI36 chr6: 42,769,519-46,417,784 , GRCh37.p13 chr6: 42,661,541-46,309,825 , GRCh38.p12 chr6: 42,693,803-46,342,088 LOC101929770, MRPS18A, 94 more genes
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