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Items: 1 to 20 of 303

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112778copy number variation1nstd102humanPathogenic GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273 LINC01742, MTCO2P1, 253 more genes
    nsv5974482insertion1nstd209human GRCh38 chr20: 62,397,927-62,397,927 , GRCh37.p13 chr20: 60,972,983-60,972,983 CABLES2
    nsv5964820copy number variation1nstd209human GRCh38 chr20: 62,406,703-62,406,754 , GRCh37.p13 chr20: 60,981,759-60,981,810 CABLES2, LOC105372709
    nsv5953343copy number variation1nstd209human GRCh38 chr20: 62,400,547-62,401,088 , GRCh37.p13 chr20: 60,975,603-60,976,144 LOC105372709, CABLES2
    nsv5669420insertion1nstd207human GRCh38 chr20: 62,397,921-62,397,921 , GRCh37.p13 chr20: 60,972,977-60,972,977 CABLES2
    nsv5669250insertion1nstd207human GRCh38 chr20: 62,397,927-62,397,927 , GRCh37.p13 chr20: 60,972,983-60,972,983 CABLES2
    nsv5664854insertion1nstd207human GRCh38 chr20: 62,398,320-62,398,320 , GRCh37.p13 chr20: 60,973,376-60,973,376 CABLES2
    nsv5664706insertion1nstd207human GRCh38 chr20: 62,398,076-62,398,076 , GRCh37.p13 chr20: 60,973,132-60,973,132 CABLES2
    nsv5381223copy number variation2nstd102humanUncertain significance GRCh37 chr20: 60,831,241-62,664,346 , GRCh38.p12 chr20: 62,256,185-64,032,993 KCNQ2-AS1, HAR1B, 100 more genes
    nsv5289201copy number variation1nstd204human GRCh38.p13 chr20: 62,058,601-62,909,300 , GRCh37.p13 chr20: 60,633,657-61,540,652 , LOC105372716, 47 more genes
    nsv5284819copy number variation1nstd204human GRCh38.p13 chr20: 62,134,401-62,423,600 , GRCh37.p13 chr20: 60,709,457-60,998,656 , RPS21, 15 more genes
    nsv5281121copy number variation1nstd204human GRCh38.p13 chr20: 62,392,130-62,393,265 , GRCh37.p13 chr20: 60,967,186-60,968,321 CABLES2
    nsv5025802copy number variation1nstd200human GRCh38 chr20: 62,404,966-62,405,131 , GRCh37.p13 chr20: 60,980,022-60,980,187 LOC105372709, CABLES2
    nsv5025801copy number variation1nstd200human GRCh38 chr20: 62,359,844-62,584,783 , GRCh37.p13 chr20|NW_003571063.2: 1-128,301 , GRCh37.p13 chr20: 61,031,539-61,181,990 LOC105372709, MIR1-1HG, 13 more genes
    nsv5025800copy number variation1nstd200human GRCh38 chr20: 62,357,913-62,396,840 , GRCh37.p13 chr20: 60,932,969-60,971,896 LOC105372708, RPS21, 2 more genes
    nsv5025798copy number variation1nstd200human GRCh38 chr20: 62,254,262-62,407,169 , GRCh37.p13 chr20: 60,829,318-60,982,225 , MIR4758, 8 more genes
    nsv5022542copy number variation1nstd200human GRCh38 chr20: 62,400,549-62,401,089 , GRCh37.p13 chr20: 60,975,605-60,976,145 LOC105372709, CABLES2
    nsv4865697copy number variation1nstd200human GRCh37 chr20: 60,980,022-60,980,187 , GRCh38.p12 chr20: 62,404,966-62,405,131 LOC105372709, CABLES2
    nsv4854156copy number variation1nstd200human GRCh37 chr20: 60,975,605-60,976,145 , GRCh38.p12 chr20: 62,400,549-62,401,089 CABLES2, LOC105372709
    nsv4768153insertion1nstd199human GRCh37 chr20: 60,972,988-60,972,988 , GRCh38.p12 chr20: 62,397,932-62,397,932 CABLES2
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