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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130769insertion1nstd186human GRCh37 chr18: 33,588,535-33,588,550 , GRCh38.p12 chr18: 36,008,572-36,008,587 RPRD1A
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv5975845insertion1nstd209human GRCh38 chr18: 36,008,577-36,008,577 , GRCh37.p13 chr18: 33,588,540-33,588,540 RPRD1A
    nsv5975724insertion1nstd209human GRCh38 chr18: 36,044,742-36,044,742 , GRCh37.p13 chr18: 33,624,705-33,624,705 RPRD1A
    nsv5932833copy number variation1nstd209human GRCh38 chr18: 36,055,900-36,055,966 , GRCh37.p13 chr18: 33,635,863-33,635,929 RPRD1A
    nsv5929426copy number variation1nstd209human GRCh38 chr18: 35,987,427-35,987,578 , GRCh37.p13 chr18: 33,567,390-33,567,541 RPRD1A
    nsv5656876insertion1nstd207human GRCh38 chr18: 36,008,577-36,008,577 , GRCh37.p13 chr18: 33,588,540-33,588,540 RPRD1A
    nsv5587429copy number variation1nstd207human GRCh38 chr18: 35,987,427-35,987,578 , GRCh37.p13 chr18: 33,567,390-33,567,541 RPRD1A
    nsv5550225insertion1nstd206human GRCh38 chr18: 36,008,572-36,008,587 , GRCh37.p13 chr18: 33,588,535-33,588,550 RPRD1A
    nsv5544283insertion1nstd206human GRCh38 chr18: 36,044,743-36,044,793 , GRCh37.p13 chr18: 33,624,706-33,624,756 RPRD1A
    nsv5532384copy number variation1nstd206human GRCh38 chr18: 35,987,428-35,987,579 , GRCh37.p13 chr18: 33,567,391-33,567,542 RPRD1A
    nsv5527577copy number variation1nstd206human GRCh38 chr18: 36,005,267-36,009,278 , GRCh37.p13 chr18: 33,585,230-33,589,241 RPRD1A
    nsv5525614copy number variation1nstd206human GRCh38 chr18: 36,016,582-36,019,095 , GRCh37.p13 chr18: 33,596,545-33,599,058 RPRD1A
    nsv5515120copy number variation1nstd206human GRCh38 chr18: 36,014,643-36,017,051 , GRCh37.p13 chr18: 33,594,606-33,597,014 RPRD1A
    nsv5350026translocation1nstd200human GRCh38 chr18: 36,055,900-36,055,900 , GRCh38 chr18: 36,055,968-36,055,968 , GRCh37.p13 chr18: 33,635,931-33,635,931 , GRCh37.p13 chr18: 33,635,863-33,635,863 RPRD1A
    nsv5350025translocation1nstd200human GRCh38 chr18: 36,005,268-36,005,268 , GRCh38 chr18: 36,009,278-36,009,278 , GRCh37.p13 chr18: 33,585,231-33,585,231 , GRCh37.p13 chr18: 33,589,241-33,589,241 RPRD1A
    nsv5350024translocation1nstd200human GRCh38 chr18: 35,987,428-35,987,428 , GRCh38 chr18: 35,987,579-35,987,579 , GRCh37.p13 chr18: 33,567,391-33,567,391 , GRCh37.p13 chr18: 33,567,542-33,567,542 RPRD1A
    nsv5339638translocation1nstd200human GRCh37 chr18: 33,635,931-33,635,931 , GRCh37 chr18: 33,635,863-33,635,863 , GRCh38.p12 chr18: 36,055,968-36,055,968 , GRCh38.p12 chr18: 36,055,900-36,055,900 RPRD1A
    nsv5320666translocation1nstd204human GRCh38.p13 chr18: 35,987,428-35,987,428 , GRCh38.p13 chr18: 35,987,579-35,987,579 , GRCh37.p13 chr18: 33,567,391-33,567,391 , GRCh37.p13 chr18: 33,567,542-33,567,542 RPRD1A
    nsv5299933copy number variation1nstd204human GRCh38.p13 chr18: 35,988,732-35,989,731 , GRCh37.p13 chr18: 33,568,695-33,569,694 RPRD1A
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