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Items: 1 to 20 of 252

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6116745mobile element insertion1nstd186human GRCh37 chr20: 25,427,039-25,427,090 , GRCh38.p12 chr20: 25,446,403-25,446,454 GINS1
    nsv5960629copy number variation1nstd209human GRCh38 chr20: 24,517,514-25,490,454 , GRCh37.p13 chr20: 24,498,150-25,471,090 LOC105372581, LOC107985402, 18 more genes
    nsv5950835copy number variation1nstd209human GRCh38 chr20: 25,433,516-25,434,174 , GRCh37.p13 chr20: 25,414,152-25,414,810 GINS1
    nsv5698681mobile element insertion2nstd211human GRCh38 chr20: 25,414,259-25,414,259 , GRCh37.p13 chr20: 25,394,895-25,394,895 GINS1
    nsv5697571mobile element insertion2nstd211human GRCh38 chr20: 25,446,403-25,446,403 , GRCh37.p13 chr20: 25,427,039-25,427,039 GINS1
    nsv5667171insertion1nstd207human GRCh38 chr20: 25,446,388-25,446,388 , GRCh37.p13 chr20: 25,427,024-25,427,024 GINS1
    nsv5533136copy number variation1nstd206human GRCh38 chr20: 25,433,518-25,434,175 , GRCh37.p13 chr20: 25,414,154-25,414,811 GINS1
    nsv5417454mobile element insertion1nstd206human GRCh38 chr20: 25,446,403-25,446,454 , GRCh37.p13 chr20: 25,427,039-25,427,090 GINS1
    nsv5365988translocation1nstd200human GRCh38 chr20: 25,416,446-25,416,446 , GRCh38 chr20: 25,420,421-25,420,421 , GRCh37.p13 chr20: 25,397,082-25,397,082 , GRCh37.p13 chr20: 25,401,057-25,401,057 GINS1
    nsv5350241translocation1nstd200human GRCh38 chr20: 25,434,175-25,434,175 , GRCh38 chr20: 25,433,518-25,433,518 , GRCh37.p13 chr20: 25,414,154-25,414,154 , GRCh37.p13 chr20: 25,414,811-25,414,811 GINS1
    nsv5196791mobile element insertion1nstd203human GRCh38 chr20: 25,446,533-25,446,549 , GRCh37.p13 chr20: 25,427,169-25,427,185 GINS1
    nsv5178864mobile element insertion1nstd203human GRCh38 chr20: 25,420,434-25,420,448 , GRCh37.p13 chr20: 25,401,070-25,401,084 GINS1
    nsv5177574mobile element insertion1nstd203human GRCh38 chr20: 25,428,969-25,428,979 , GRCh37.p13 chr20: 25,409,605-25,409,615 GINS1
    nsv5176436mobile element insertion1nstd203human GRCh38 chr20: 25,427,888-25,427,910 , GRCh37.p13 chr20: 25,408,524-25,408,546 GINS1
    nsv5171315mobile element insertion1nstd203human GRCh38 chr20: 25,445,513-25,445,528 , GRCh37.p13 chr20: 25,426,149-25,426,164 GINS1
    nsv5167923mobile element insertion1nstd203human GRCh38 chr20: 25,423,593-25,423,610 , GRCh37.p13 chr20: 25,404,229-25,404,246 GINS1
    nsv5164329mobile element insertion1nstd203human GRCh38 chr20: 25,446,388-25,446,403 , GRCh37.p13 chr20: 25,427,024-25,427,039 GINS1
    nsv5160710mobile element insertion1nstd203human GRCh38 chr20: 25,414,243-25,414,259 , GRCh37.p13 chr20: 25,394,879-25,394,895 GINS1
    nsv5025239copy number variation1nstd200human GRCh38 chr20: 25,440,069-25,447,294 , GRCh37.p13 chr20: 25,420,705-25,427,930 GINS1
    nsv5021836copy number variation1nstd200human GRCh38 chr20: 25,443,385-25,455,278 , GRCh37.p13 chr20: 25,424,021-25,435,914 NINL, GINS1
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