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Items: 1 to 20 of 502

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5967784inversion1nstd209human GRCh38 chr22: 20,337,735-21,327,040 , GRCh37.p13 chr22: 20,325,258-21,681,329 , CRKL, 49 more genes
    nsv5673274copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,893,882-21,563,420 , GRCh38.p12 chr22: 18,339,130-21,209,131 UFD1-AS1, LOC100129254, 129 more genes
    nsv5673185copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,893,882-21,571,027 , GRCh38.p12 chr22: 18,339,130-21,216,738 CCDC188, LOC107987325, 129 more genes
    nsv5672103inversion1nstd207human GRCh38 chr22: 21,151,085-21,458,186 , GRCh37.p13 chr22: 21,505,374-21,812,475 , HIC2, 13 more genes
    nsv5599070copy number variation1nstd207human GRCh38 chr22: 21,207,137-21,207,204 , GRCh37.p13 chr22: 21,561,426-21,561,493 GGT2P
    nsv5590985copy number variation1nstd207human GRCh38 chr22: 21,236,136-21,236,270 , GRCh37.p13 chr22: 21,590,425-21,590,559 GGT2P
    nsv5546016copy number variation1nstd206human GRCh38 chr22: 20,689,282-21,312,400 , GRCh37.p13 chr22: 21,043,570-21,666,689 , BCRP2, 30 more genes
    nsv5535972copy number variation1nstd206human GRCh38 chr22: 20,679,564-21,209,564 , GRCh37.p13 chr22: 21,033,852-21,563,853 , PI4KA, 26 more genes
    nsv5299317copy number variation1nstd204human GRCh38.p13 chr22: 21,251,901-21,254,900 , GRCh37.p13 chr22: 21,606,190-21,609,189 GGT2P
    nsv5298772copy number variation1nstd204human GRCh38.p13 chr22: 21,240,401-21,241,300 , GRCh37.p13 chr22: 21,594,690-21,595,589 GGT2P
    nsv5298047copy number variation1nstd204human GRCh38.p13 chr22: 21,259,401-21,263,300 , GRCh37.p13 chr22: 21,613,690-21,617,589 GGT2P
    nsv5297757copy number variation1nstd204human GRCh38.p13 chr22: 21,274,001-21,278,100 , GRCh37.p13 chr22: 21,628,290-21,632,389 GGT2P
    nsv5297402copy number variation1nstd204human GRCh38.p13 chr22: 21,216,533-21,218,036 , GRCh37.p13 chr22: 21,570,822-21,572,325 GGT2P
    nsv5297383copy number variation1nstd204human GRCh38.p13 chr22: 21,216,901-21,221,200 , GRCh37.p13 chr22: 21,571,190-21,575,489 GGT2P
    nsv5296628copy number variation1nstd204human GRCh38.p13 chr22: 21,257,101-21,257,500 , GRCh37.p13 chr22: 21,611,390-21,611,789 GGT2P
    nsv5295838copy number variation1nstd204human GRCh38.p13 chr22: 21,230,001-21,233,700 , GRCh37.p13 chr22: 21,584,290-21,587,989 GGT2P
    nsv5295609copy number variation1nstd204human GRCh38.p13 chr22: 21,233,701-21,234,700 , GRCh37.p13 chr22: 21,587,990-21,588,989 GGT2P
    nsv5294984copy number variation1nstd204human GRCh38.p13 chr22: 21,248,701-21,250,400 , GRCh37.p13 chr22: 21,602,990-21,604,689 GGT2P
    nsv5293835copy number variation1nstd204human GRCh38.p13 chr22: 21,251,901-21,252,700 , GRCh37.p13 chr22: 21,606,190-21,606,989 GGT2P
    nsv5293508copy number variation1nstd204human GRCh38.p13 chr22: 21,267,801-21,269,600 , GRCh37.p13 chr22: 21,622,090-21,623,889 E2F6P3, GGT2P
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