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Items: 1 to 20 of 204

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095898copy number variation1nstd102humanPathogenic GRCh37 chr20: 42,223,339-44,638,757 , GRCh38.p12 chr20: 43,594,699-46,010,118 ADA, CCN5, 99 more genes
    nsv7062736inversion1nstd229human GRCh38 chr20: 36,955,253-45,585,462 , GRCh37.p13 chr20: 35,583,656-44,214,101 GDAP1L1, PI3, 177 more genes
    nsv7035244copy number variation1nstd229human GRCh38 chr20: 44,894,416-44,942,850 , GRCh37.p13 chr20: 43,523,057-43,571,491 YWHAB, PABPC1L, 1 more genes
    nsv7029654copy number variation1nstd229human GRCh38 chr20: 44,935,137-44,935,187 , GRCh37.p13 chr20: 43,563,778-43,563,828 PABPC1L
    nsv7028635copy number variation1nstd229human GRCh38 chr20: 44,924,922-44,925,099 , GRCh37.p13 chr20: 43,553,563-43,553,740 PABPC1L
    nsv7022461copy number variation1nstd229human GRCh38 chr20: 44,922,560-44,922,905 , GRCh37.p13 chr20: 43,551,201-43,551,546 PABPC1L
    nsv6626702copy number variation1nstd224human GRCh37 chr20: 43,530,403-43,580,118 , GRCh38.p12 chr20: 44,901,762-44,951,477 TOMM34, PABPC1L, 1 more genes
    nsv6626701copy number variation2nstd224human GRCh37 chr20: 43,530,403-43,567,320 , GRCh38.p12 chr20: 44,901,762-44,938,679 YWHAB, PABPC1L
    nsv6596116inversion1nstd223human GRCh38 chr20: 36,955,253-45,585,469 , GRCh37.p13 chr20: 35,583,656-44,214,108 LOC101929863, LOC105372620, 177 more genes
    nsv6550090copy number variation1nstd223human GRCh38 chr20: 44,894,362-44,942,872 , GRCh37.p13 chr20: 43,523,003-43,571,513 YWHAB, TOMM34, 1 more genes
    nsv6543726copy number variation1nstd223human GRCh38 chr20: 44,924,922-44,925,099 , GRCh37.p13 chr20: 43,553,563-43,553,740 PABPC1L
    nsv6290315copy number variation1nstd102humanPathogenic GRCh37 chr20: 42,985,044-48,599,046 , GRCh38.p12 chr20: 44,356,404-49,982,509 PABPC1L, LOC107985401, 170 more genes
    nsv6224541copy number variation1nstd214human GRCh38 chr20: 44,931,106-44,931,156 , GRCh37.p13 chr20: 43,559,747-43,559,797 PABPC1L
    nsv6134164copy number variation1nstd213human GRCh37 chr20: 43,170,000-44,070,001 , GRCh38.p12 chr20: 44,541,359-45,441,361 PI3, SEMG2, 35 more genes
    nsv5976704inversion1nstd209human GRCh38 chr20: 36,955,252-45,585,469 , GRCh37.p13 chr20: 35,583,655-44,214,108 , ADA, 180 more genes
    nsv5975827insertion1nstd209human GRCh38 chr20: 44,931,042-44,931,042 , GRCh37.p13 chr20: 43,559,683-43,559,683 PABPC1L
    nsv5956231copy number variation1nstd209human GRCh38 chr20: 44,924,922-44,925,098 , GRCh37.p13 chr20: 43,553,563-43,553,739 PABPC1L
    nsv5952055copy number variation1nstd209human GRCh38 chr20: 44,920,869-44,921,205 , GRCh37.p13 chr20: 43,549,510-43,549,846 PABPC1L
    nsv5604383copy number variation1nstd207human GRCh38 chr20: 44,931,102-44,931,156 , GRCh37.p13 chr20: 43,559,743-43,559,797 PABPC1L
    nsv5593371copy number variation1nstd207human GRCh38 chr20: 44,924,922-44,925,098 , GRCh37.p13 chr20: 43,553,563-43,553,739 PABPC1L
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