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Items: 1 to 20 of 388

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5963791copy number variation1nstd209human GRCh38 chr22: 21,924,820-21,925,145 , GRCh37.p13 chr22: 22,279,193-22,279,518 PPM1F
    nsv5959856copy number variation1nstd209human GRCh38 chr22: 21,951,192-21,951,423 , GRCh37.p13 chr22: 22,305,564-22,305,795 PPM1F
    nsv5670478insertion1nstd207human GRCh38 chr22: 21,921,194-21,921,194 , GRCh37.p13 chr22: 22,275,567-22,275,567 PPM1F
    nsv5549689copy number variation1nstd206human GRCh38 chr22: 21,942,750-21,942,819 , GRCh37.p13 chr22: 22,297,122-22,297,191 PPM1F, PPM1F-AS1
    nsv5536323copy number variation1nstd206human GRCh38 chr22: 21,907,467-21,919,734 , GRCh37.p13 chr22: 22,261,807-22,274,107 PPM1F
    nsv5299735copy number variation1nstd204human GRCh38.p13 chr22: 21,948,572-21,953,403 , GRCh37.p13 chr22: 22,302,944-22,307,775 PPM1F
    nsv5296855copy number variation1nstd204human GRCh38.p13 chr22: 21,892,285-21,924,252 , GRCh37.p13 chr22: 22,246,618-22,278,625 PPM1F
    nsv5193537mobile element insertion1nstd203human GRCh38 chr22: 21,950,391-21,950,401 , GRCh37.p13 chr22: 22,304,763-22,304,773 PPM1F
    nsv4869356copy number variation1nstd200human GRCh37 chr22: 22,174,827-22,404,189 , GRCh38.p12 chr22: 21,820,538-22,049,791 IGLVI-70, MAPK1, 8 more genes
    nsv4768383copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-26,483,608 , GRCh38.p12 chr22: 16,408,173-26,087,642 KRT18P62, LOC101060852, 437 more genes
    nsv4730001copy number variation1nstd102humanPathogenic GRCh37 chr22: 19,035,089-22,672,555 , GRCh38.p12 chr22: 18,339,130-22,318,200 C22orf39, IGLL4P, 191 more genes
    nsv4729926copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824 FBXO7, GTSE1, 1084 more genes
    nsv4729903copy number variation1nstd102humanUncertain significance GRCh37 chr22: 22,079,945-22,587,762 , GRCh38.p12 chr22: 21,725,656-22,233,351 IGLVV-58, IGLV6-57, 33 more genes
    nsv4729862copy number variation1nstd102humanPathogenic GRCh37 chr22: 21,798,906-23,805,099 , GRCh38.p12 chr22: 21,444,617-23,462,912 LL22NC03-63E9.3, IGLC4, 158 more genes
    nsv4685622copy number variation1nstd102humanPathogenic GRCh37 chr22: 21,822,774-23,025,613 , GRCh38.p12 chr22: 21,468,485-22,683,141 BMS1P20, IGLV3-29, 90 more genes
    nsv4684353copy number variation1nstd102humanPathogenic GRCh37 chr22: 21,979,096-22,941,426 , GRCh38.p12 chr22: 21,624,807-22,598,956 IGLV2-33, IGLVIV-64, 74 more genes
    nsv4680965copy number variation1nstd189human GRCh37.p13 chr22: 22,265,332-22,571,586 , GRCh38.p12 chr22: 21,910,992-22,217,194 IGL, TOP3B, 27 more genes
    nsv4680517copy number variation1nstd189human GRCh37.p13 chr22: 22,284,175-22,571,586 , GRCh38.p12 chr22: 21,929,803-22,217,194 IGL, TOP3B, 27 more genes
    nsv4680439copy number variation1nstd189human GRCh37.p13 chr22: 22,202,778-22,537,603 , GRCh38.p12 chr22: 21,848,489-22,183,213 IGL, MAPK1, 22 more genes
    nsv4680421copy number variation1nstd189human GRCh37.p13 chr22: 21,458,444-22,984,438 , GRCh38.p12 chr22: 21,104,155-22,641,967 , BCRP4, 102 more genes
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