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Items: 1 to 20 of 177

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137049copy number variation1nstd102humanPathogenic GRCh37 chr6: 393,153-3,751,765 , GRCh38.p12 chr6: 393,153-3,751,531 LOC105374883, LINC02525, 57 more genes
    nsv7093363copy number variation1nstd102humanPathogenic GRCh37 chr6: 820,000-21,700,000 , GRCh38.p12 chr6: 820,000-21,699,769 LOC101928354, CNN3P1, 321 more genes
    nsv7054186inversion1nstd229human GRCh38 chr6: 3,021,884-3,024,567 , GRCh37.p13 chr6: 3,022,118-3,024,801 HTATSF1P2, LOC101927759
    nsv7053151inversion1nstd229human GRCh38 chr6: 2,903,156-3,064,183 , GRCh37.p13 chr6: 2,903,390-3,064,417 SERPINB8P1, NQO2, 8 more genes
    nsv7053065inversion1nstd229human GRCh38 chr6: 3,003,253-3,052,541 , GRCh37.p13 chr6: 3,003,487-3,052,775 NQO2, FAM136BP, 3 more genes
    nsv7050130inversion1nstd229human GRCh38 chr6: 3,020,084-3,032,377 , GRCh37.p13 chr6: 3,020,318-3,032,611 NQO2, LOC101927759, 1 more genes
    nsv7047929inversion1nstd229human GRCh38 chr6: 2,249,577-5,332,355 , GRCh37.p13 chr6: 2,249,811-5,332,588 LOC107986561, NQO2-AS1, 67 more genes
    nsv7044205inversion1nstd229human GRCh38 chr6: 2,472,898-4,774,625 , GRCh37.p13 chr6: 2,473,132-4,774,859 TOMM5P1, PXDC1, 56 more genes
    nsv6785298copy number variation1nstd229human GRCh38 chr6: 2,759,301-4,105,800 , GRCh37.p13 chr6: 2,759,535-4,106,034 LOC107986557, SERPINB9-AS1, 39 more genes
    nsv6780901copy number variation1nstd229human GRCh38 chr6: 3,024,543-3,048,077 , GRCh37.p13 chr6: 3,024,777-3,048,311 LOC101927759, FAM136BP, 1 more genes
    nsv6636564copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,975-3,718,881 , GRCh38.p12 chr6: 156,975-3,718,647 LOC101927691, LOC107986555, 60 more genes
    nsv6568887inversion1nstd223human GRCh38 chr6: 2,903,210-3,064,173 , GRCh37.p13 chr6: 2,903,444-3,064,407 FAM136BP, LINC01011, 8 more genes
    nsv6563981inversion1nstd223human GRCh38 chr6: 3,004,611-3,051,208 , GRCh37.p13 chr6: 3,004,845-3,051,442 NQO2, SERPINB8P1, 3 more genes
    nsv6558574inversion1nstd223human GRCh38 chr6: 2,998,034-3,056,986 , GRCh37.p13 chr6: 2,998,268-3,057,220 NQO2, SERPINB8P1, 4 more genes
    nsv6557901inversion1nstd223human GRCh38 chr6: 3,003,274-3,052,507 , GRCh37.p13 chr6: 3,003,508-3,052,741 NQO2, SERPINB8P1, 3 more genes
    nsv6400658copy number variation1nstd223human GRCh38 chr6: 2,956,035-3,081,695 , GRCh37.p13 chr6: 2,956,269-3,081,929 SERPINB6, FAM136BP, 7 more genes
    nsv6314746copy number variation1nstd102humanPathogenic GRCh37 chr6: 375,263-3,655,142 , GRCh38.p12 chr6: 375,263-3,654,908 RN7SL352P, SERPINB8P1, 55 more genes
    nsv6313679copy number variation1nstd102humanPathogenic GRCh37 chr6: 383,951-3,898,619 , GRCh38.p12 chr6: 383,951-3,898,385 SERPINB9P1, LOC101927691, 59 more genes
    nsv6300835copy number variation1nstd186human GRCh37 chr6: 3,026,697-3,026,811 , GRCh38.p12 chr6: 3,026,463-3,026,577 LOC101927759
    nsv6147176inversion1nstd206human GRCh38 chr6: 3,002,568-3,053,212 , GRCh37.p13 chr6: 3,002,802-3,053,446 NQO2, SERPINB8P1, 3 more genes
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