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Items: 1 to 20 of 184

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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
    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
    nsv7042784inversion1nstd229human GRCh38 chr6: 2,599,103-2,898,736 , GRCh37.p13 chr6: 2,599,337-2,898,970 SERPINB1, SERPINB9P1, 7 more genes
    nsv6796411copy number variation1nstd229human GRCh38 chr6: 2,161,102-2,622,508 , GRCh37.p13 chr6: 2,161,336-2,622,742 GMDS-DT, LOC107986512, 3 more genes
    nsv6787032copy number variation1nstd229human GRCh38 chr6: 2,627,864-2,633,189 , GRCh37.p13 chr6: 2,628,098-2,633,423 LINC02521, LINC01600
    nsv6785318copy number variation1nstd229human GRCh38 chr6: 2,575,801-2,655,600 , GRCh37.p13 chr6: 2,576,035-2,655,834 LINC01600, LINC02521
    nsv6782763copy number variation1nstd229human GRCh38 chr6: 2,092,701-2,636,100 , GRCh37.p13 chr6: 2,092,935-2,636,334 GMDS-DT, LOC107986512, 4 more genes
    nsv6779522copy number variation1nstd229human GRCh38 chr6: 2,620,112-2,620,142 , GRCh37.p13 chr6: 2,620,346-2,620,376 LINC01600
    nsv6636569copy number variation1nstd102humanUncertain significance GRCh37 chr6: 2,162,500-2,864,248 , GRCh38.p12 chr6: 2,162,266-2,864,014 GMDS-DT, SERPINB9P1, 9 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
    nsv6631210copy number variation1nstd224human GRCh37 chr6: 1,633,682-2,893,647 , GRCh38.p12 chr6: 1,633,447-2,893,413 SERPINB1, SERPINB9P1, 12 more genes
    nsv6412123copy number variation1nstd223human GRCh38 chr6: 2,623,169-2,625,285 , GRCh37.p13 chr6: 2,623,403-2,625,519 LINC01600
    nsv6401891copy number variation1nstd223human GRCh38 chr6: 2,627,864-2,633,188 , GRCh37.p13 chr6: 2,628,098-2,633,422 LINC01600, LINC02521
    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
    nsv6290973copy number variation1nstd102humanLikely benign GRCh37 chr6: 2,370,075-2,688,038 , GRCh38.p12 chr6: 2,369,841-2,687,804 LINC02521, LINC01600, 2 more genes
    nsv6136505copy number variation1nstd213human GRCh37 chr6: 380,000-11,010,001 , GRCh38.p12 chr6: 380,000-11,009,768 BMP6, BPHL, 178 more genes
    nsv6135513copy number variation1nstd213human GRCh37 chr6: 380,000-10,980,001 , GRCh38.p12 chr6: 380,000-10,979,768 BMP6, BPHL, 178 more genes
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