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Items: 1 to 20 of 589

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147134insertion1nstd232human GRCh37.p13 chr20: 42,690,176-42,690,176 , GRCh38.p12 chr20: 44,061,536-44,061,536 TOX2
    nsv7140020insertion1nstd232human GRCh37.p13 chr20: 42,676,132-42,676,132 , GRCh38.p12 chr20: 44,047,492-44,047,492 TOX2
    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
    nsv7077664inversion1nstd229human GRCh38 chr20: 43,980,129-43,988,233 , GRCh37.p13 chr20: 42,608,769-42,616,873 TOX2
    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
    nsv7038021copy number variation1nstd229human GRCh38 chr20: 44,044,505-44,054,944 , GRCh37.p13 chr20: 42,673,145-42,683,584 TOX2
    nsv7033382copy number variation1nstd229human GRCh38 chr20: 44,036,100-44,043,733 , GRCh37.p13 chr20: 42,664,740-42,672,373 TOX2
    nsv7031411copy number variation1nstd229human GRCh38 chr20: 43,969,074-43,969,210 , GRCh37.p13 chr20: 42,597,714-42,597,850 TOX2
    nsv7029938copy number variation1nstd229human GRCh38 chr20: 44,063,772-44,063,805 , GRCh37.p13 chr20: 42,692,412-42,692,445 TOX2
    nsv7028962copy number variation1nstd229human GRCh38 chr20: 44,009,628-44,010,012 , GRCh37.p13 chr20: 42,638,268-42,638,652 TOX2
    nsv7028619copy number variation1nstd229human GRCh38 chr20: 43,922,512-43,925,551 , GRCh37.p13 chr20: 42,551,152-42,554,191 TOX2
    nsv7025348copy number variation1nstd229human GRCh38 chr20: 43,934,612-43,938,066 , GRCh37.p13 chr20: 42,563,252-42,566,706 TOX2
    nsv7024378copy number variation1nstd229human GRCh38 chr20: 44,042,701-44,052,500 , GRCh37.p13 chr20: 42,671,341-42,681,140 TOX2
    nsv7023887copy number variation1nstd229human GRCh38 chr20: 44,047,488-44,047,888 , GRCh37.p13 chr20: 42,676,128-42,676,528 TOX2
    nsv7022254copy number variation1nstd229human GRCh38 chr20: 44,057,560-44,057,620 , GRCh37.p13 chr20: 42,686,200-42,686,260 TOX2
    nsv7020690copy number variation1nstd229human GRCh38 chr20: 43,954,911-43,954,972 , GRCh37.p13 chr20: 42,583,551-42,583,612 TOX2
    nsv7018529copy number variation1nstd229human GRCh38 chr20: 44,027,775-44,045,126 , GRCh37.p13 chr20: 42,656,415-42,673,766 TOX2
    nsv6596116inversion1nstd223human GRCh38 chr20: 36,955,253-45,585,469 , GRCh37.p13 chr20: 35,583,656-44,214,108 LOC101929863, LOC105372620, 177 more genes
    nsv6553890copy number variation1nstd223human GRCh38 chr20: 44,024,100-44,026,382 , GRCh37.p13 chr20: 42,652,740-42,655,022 TOX2
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