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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
    nsv7073834inversion1nstd229human GRCh38 chr20: 39,260,815-44,460,004 , GRCh37.p13 chr20: 37,889,458-43,088,644 LOC100128988, LOC100419859, 72 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
    nsv7037661copy number variation1nstd229human GRCh38 chr20: 44,283,465-44,467,234 , GRCh37.p13 chr20: 42,912,105-43,095,874 MIR3646, FITM2, 7 more genes
    nsv7034803copy number variation1nstd229human GRCh38 chr20: 44,373,292-44,382,382 , GRCh37.p13 chr20: 43,001,932-43,011,022 HNF4A, HNF4A-AS1
    nsv7032351copy number variation1nstd229human GRCh38 chr20: 44,184,970-44,592,264 , GRCh37.p13 chr20: 42,813,610-43,220,905 SERINC3, JPH2, 14 more genes
    nsv7029975copy number variation1nstd229human GRCh38 chr20: 44,391,734-44,391,960 , GRCh37.p13 chr20: 43,020,374-43,020,600 HNF4A-AS1, HNF4A
    nsv7021430copy number variation1nstd229human GRCh38 chr20: 44,373,862-44,379,951 , GRCh37.p13 chr20: 43,002,502-43,008,591 HNF4A-AS1, HNF4A
    nsv7020876copy number variation1nstd229human GRCh38 chr20: 44,390,365-44,393,354 , GRCh37.p13 chr20: 43,019,005-43,021,994 HNF4A-AS1, HNF4A
    nsv7019608copy number variation1nstd229human GRCh38 chr20: 44,377,109-44,380,830 , GRCh37.p13 chr20: 43,005,749-43,009,470 HNF4A-AS1, HNF4A
    nsv6596116inversion1nstd223human GRCh38 chr20: 36,955,253-45,585,469 , GRCh37.p13 chr20: 35,583,656-44,214,108 LOC101929863, LOC105372620, 177 more genes
    nsv6550262copy number variation1nstd223human GRCh38 chr20: 44,377,109-44,380,826 , GRCh37.p13 chr20: 43,005,749-43,009,466 HNF4A-AS1, HNF4A
    nsv6545693copy number variation1nstd223human GRCh38 chr20: 44,393,639-44,393,931 , GRCh37.p13 chr20: 43,022,279-43,022,571 HNF4A, HNF4A-AS1
    nsv6538801copy number variation1nstd223human GRCh38 chr20: 44,373,862-44,379,951 , GRCh37.p13 chr20: 43,002,502-43,008,591 HNF4A, HNF4A-AS1
    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
    nsv6134298copy number variation1nstd213human GRCh37 chr20: 42,740,000-43,170,001 , GRCh38.p12 chr20: 44,111,360-44,541,360 OSER1, JPH2, 14 more genes
    nsv6134297copy number variation1nstd213human GRCh37 chr20: 42,590,000-43,450,001 , GRCh38.p12 chr20: 43,961,360-44,821,360 ADA, OSER1, 22 more genes
    nsv5976704inversion1nstd209human GRCh38 chr20: 36,955,252-45,585,469 , GRCh37.p13 chr20: 35,583,655-44,214,108 , ADA, 180 more genes
    nsv5974273insertion1nstd209human GRCh38 chr20: 44,388,380-44,388,380 , GRCh37.p13 chr20: 43,017,020-43,017,020 HNF4A, HNF4A-AS1
    nsv5964345copy number variation1nstd209human GRCh38 chr20: 44,388,838-44,388,899 , GRCh37.p13 chr20: 43,017,478-43,017,539 HNF4A, HNF4A-AS1
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