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Items: 1 to 20 of 179

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076611inversion1nstd229human GRCh38 chr20: 49,933,112-49,934,640 , GRCh37.p13 chr20: 48,549,649-48,551,177 RNF114
    nsv7075103inversion1nstd229human GRCh38 chr20: 48,844,229-55,780,453 , GRCh37.p13 chr20: 47,460,766-54,355,509 RPL12P4, LOC105372664, 113 more genes
    nsv7071042inversion1nstd229human GRCh38 chr20: 49,933,145-49,934,602 , GRCh37.p13 chr20: 48,549,682-48,551,139 RNF114
    nsv7065344inversion1nstd229human GRCh38 chr20: 49,128,244-52,291,086 , GRCh37.p13 chr20: 47,744,781-50,907,625 PARD6B, LOC105372657, 77 more genes
    nsv7064075inversion1nstd229human GRCh38 chr20: 49,009,324-55,851,498 , GRCh37.p13 chr20: 47,625,861-54,426,554 DPM1, KCNG1, 115 more genes
    nsv7036403copy number variation1nstd229human GRCh38 chr20: 49,945,666-49,946,200 , GRCh37.p13 chr20: 48,562,203-48,562,737 RNF114
    nsv7036271copy number variation1nstd229human GRCh38 chr20: 49,941,619-49,947,120 , GRCh37.p13 chr20: 48,558,156-48,563,657 RNF114
    nsv7032036copy number variation1nstd229human GRCh38 chr20: 49,925,474-49,943,383 , GRCh37.p13 chr20: 48,542,011-48,559,920 LOC105372653, RNF114
    nsv7028111copy number variation1nstd229human GRCh38 chr20: 49,878,701-50,092,300 , GRCh37.p13 chr20: 48,495,238-48,708,837 SPATA2, UBE2V1, 10 more genes
    nsv7026143copy number variation1nstd229human GRCh38 chr20: 49,936,364-49,938,899 , GRCh37.p13 chr20: 48,552,901-48,555,436 RNF114
    nsv7025089copy number variation1nstd229human GRCh38 chr20: 49,903,525-49,972,468 , GRCh37.p13 chr20: 48,520,062-48,589,005 KRT18P4, RNU6-147P, 3 more genes
    nsv7024518copy number variation1nstd229human GRCh38 chr20: 49,946,894-49,947,346 , GRCh37.p13 chr20: 48,563,431-48,563,883 RNF114
    nsv7020409copy number variation1nstd229human GRCh38 chr20: 49,428,501-51,120,300 , GRCh37.p13 chr20: 48,045,038-49,736,837 LOC100421569, RNU6-147P, 54 more genes
    nsv7018563copy number variation1nstd229human GRCh38 chr20: 49,934,153-49,935,065 , GRCh37.p13 chr20: 48,550,690-48,551,602 RNF114
    nsv6638039copy number variation1nstd102humanUncertain significance GRCh37 chr20: 48,352,572-48,766,664 , GRCh38.p12 chr20: 49,736,035-50,150,127 KRT18P4, LOC105372655, 16 more genes
    nsv6599991inversion1nstd223human GRCh38 chr20: 49,933,118-49,934,654 , GRCh37.p13 chr20: 48,549,655-48,551,191 RNF114
    nsv6540686copy number variation1nstd223human GRCh38 chr20: 49,945,566-49,946,001 , GRCh37.p13 chr20: 48,562,103-48,562,538 RNF114
    nsv6536699copy number variation1nstd223human GRCh38 chr20: 49,934,153-49,935,065 , GRCh37.p13 chr20: 48,550,690-48,551,602 RNF114
    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
    nsv6251499mobile element insertion1nstd215human GRCh38 chr20: 49,947,226-49,947,226 , GRCh37.p13 chr20: 48,563,763-48,563,763 RNF114
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