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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5904221copy number variation1nstd209human GRCh38 chr6: 47,596,993-47,599,173 , GRCh37.p13 chr6: 47,564,729-47,566,909 CD2AP, LOC100421517
    nsv5888957copy number variation1nstd209human GRCh38 chr6: 47,575,691-47,575,827 , GRCh37.p13 chr6: 47,543,427-47,543,563 CD2AP
    nsv5845624copy number variation1nstd209human GRCh38 chr6: 47,597,018-47,599,217 , GRCh37.p13 chr6: 47,564,754-47,566,953 CD2AP, LOC100421517
    nsv5691070mobile element insertion1nstd211human GRCh38 chr6: 47,549,397-47,549,397 , GRCh37.p13 chr6: 47,517,133-47,517,133 CD2AP
    nsv5683080mobile element insertion1nstd211human GRCh38 chr6: 47,488,044-47,488,044 , GRCh37.p13 chr6: 47,455,780-47,455,780 CD2AP
    nsv5638789insertion1nstd207human GRCh38 chr6: 47,505,616-47,505,616 , GRCh37.p13 chr6: 47,473,352-47,473,352 CD2AP
    nsv5629646insertion1nstd207human GRCh38 chr6: 47,485,653-47,485,653 , GRCh37.p13 chr6: 47,453,389-47,453,389 CD2AP
    nsv5581332copy number variation1nstd207human GRCh38 chr6: 47,596,993-47,599,173 , GRCh37.p13 chr6: 47,564,729-47,566,909 LOC100421517, CD2AP
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5553891insertion1nstd206human GRCh38 chr6: 47,602,589-47,602,625 , GRCh37.p13 chr6: 47,570,325-47,570,361 CD2AP
    nsv5471657copy number variation1nstd206human GRCh38 chr6: 47,596,994-47,599,174 , GRCh37.p13 chr6: 47,564,730-47,566,910 LOC100421517, CD2AP
    nsv5470968copy number variation1nstd206human GRCh38 chr6: 47,585,557-47,585,613 , GRCh37.p13 chr6: 47,553,293-47,553,349 CD2AP
    nsv5470489copy number variation1nstd206human GRCh38 chr6: 47,575,693-47,575,828 , GRCh37.p13 chr6: 47,543,429-47,543,564 CD2AP
    nsv5410085mobile element insertion1nstd206human GRCh38 chr6: 47,569,434-47,569,434 , GRCh37.p13 chr6: 47,537,170-47,537,170 CD2AP
    nsv5399798mobile element insertion1nstd206human GRCh38 chr6: 47,549,397-47,549,415 , GRCh37.p13 chr6: 47,517,133-47,517,151 CD2AP
    nsv5319500copy number variation1nstd204human GRCh37.p13 chr6: 47,564,730-47,566,910 , GRCh38.p13 chr6: 47,596,994-47,599,174 LOC100421517, CD2AP
    nsv5233560copy number variation1nstd204human GRCh38.p13 chr6: 47,597,001-47,600,400 , GRCh37.p13 chr6: 47,564,737-47,568,136 CD2AP, LOC100421517
    nsv5232739copy number variation1nstd204human GRCh38.p13 chr6: 47,490,401-47,493,800 , GRCh37.p13 chr6: 47,458,137-47,461,536 CD2AP
    nsv5230113copy number variation1nstd204human GRCh38.p13 chr6: 47,597,001-47,597,600 , GRCh37.p13 chr6: 47,564,737-47,565,336 LOC100421517, CD2AP
    nsv5222238copy number variation1nstd204human GRCh38.p13 chr6: 47,596,968-47,599,217 , GRCh37.p13 chr6: 47,564,704-47,566,953 CD2AP, LOC100421517
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