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Items: 1 to 20 of 175

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5903298copy number variation1nstd209human GRCh38 chr6: 158,949,237-158,950,567 , GRCh37.p13 chr6: 159,370,269-159,371,599 RSPH3
    nsv5894282copy number variation1nstd209human GRCh38 chr6: 158,998,114-158,999,298 , GRCh37.p13 chr6: 159,419,146-159,420,330 RSPH3, TAGAP-AS1
    nsv5891760copy number variation1nstd209human GRCh38 chr6: 158,997,850-158,998,677 , GRCh37.p13 chr6: 159,418,882-159,419,709 RSPH3, TAGAP-AS1
    nsv5844150copy number variation1nstd209human GRCh38 chr6: 158,949,157-158,950,656 , GRCh37.p13 chr6: 159,370,189-159,371,688 RSPH3
    nsv5675825mobile element insertion1nstd211human GRCh38 chr6: 158,997,851-158,997,851 , GRCh37.p13 chr6: 159,418,883-159,418,883 RSPH3
    nsv5473760copy number variation1nstd206human GRCh38 chr6: 158,984,450-158,984,673 , GRCh37.p13 chr6: 159,405,482-159,405,705 RSPH3
    nsv5473147copy number variation1nstd206human GRCh38 chr6: 159,000,389-159,000,439 , GRCh37.p13 chr6: 159,421,421-159,421,471 TAGAP-AS1, RSPH3
    nsv5472373copy number variation1nstd206human GRCh38 chr6: 158,964,190-158,964,441 , GRCh37.p13 chr6: 159,385,222-159,385,473 RSPH3
    nsv5469551copy number variation1nstd206human GRCh38 chr6: 158,949,239-158,950,568 , GRCh37.p13 chr6: 159,370,271-159,371,600 RSPH3
    nsv5464449copy number variation1nstd206human GRCh38 chr6: 158,971,707-158,973,722 , GRCh37.p13 chr6: 159,392,739-159,394,754 RSPH3
    nsv5463920copy number variation1nstd206human GRCh38 chr6: 158,998,327-158,998,584 , GRCh37.p13 chr6: 159,419,359-159,419,616 RSPH3, TAGAP-AS1
    nsv5388611copy number variation1nstd186human GRCh37 chr6: 159,418,883-159,419,710 , GRCh38.p12 chr6: 158,997,851-158,998,678 RSPH3, TAGAP-AS1
    nsv5369986translocation1nstd200human GRCh38 chr6: 158,998,122-158,998,122 , GRCh38 chr6: 158,999,299-158,999,299 , GRCh37.p13 chr6: 159,419,154-159,419,154 , GRCh37.p13 chr6: 159,420,331-159,420,331 RSPH3, TAGAP-AS1
    nsv5369985translocation1nstd200human GRCh38 chr6: 158,959,409-158,959,409 , GRCh38 chr6: 158,959,940-158,959,940 , GRCh37.p13 chr6: 159,380,972-159,380,972 , GRCh37.p13 chr6: 159,380,441-159,380,441 RSPH3
    nsv5333914translocation1nstd200human GRCh37 chr6: 159,419,154-159,419,154 , GRCh37 chr6: 159,420,331-159,420,331 , GRCh38.p12 chr6: 158,998,122-158,998,122 , GRCh38.p12 chr6: 158,999,299-158,999,299 RSPH3, TAGAP-AS1
    nsv5327743translocation1nstd204human GRCh37.p13 chr6: 159,419,154-159,419,154 , GRCh37.p13 chr6: 159,420,331-159,420,331 , GRCh38.p13 chr6: 158,999,299-158,999,299 , GRCh38.p13 chr6: 158,998,122-158,998,122 RSPH3, TAGAP-AS1
    nsv5309500copy number variation1nstd204human GRCh37.p13 chr6: 159,419,093-159,419,849 , GRCh38.p13 chr6: 158,998,061-158,998,817 RSPH3, TAGAP-AS1
    nsv5106228mobile element insertion1nstd203human GRCh38 chr6: 158,949,345-158,949,347 , GRCh37.p13 chr6: 159,370,377-159,370,379 RSPH3
    nsv4943682copy number variation1nstd200human GRCh38 chr6: 158,997,851-158,998,678 , GRCh37.p13 chr6: 159,418,883-159,419,710 RSPH3, TAGAP-AS1
    nsv4943681copy number variation1nstd200human GRCh38 chr6: 158,984,450-158,984,673 , GRCh37.p13 chr6: 159,405,482-159,405,705 RSPH3
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