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Items: 1 to 20 of 513

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147809insertion1nstd232human GRCh37.p13 chr20: 36,361,470-36,361,470 , GRCh38.p12 chr20: 37,733,068-37,733,068 CTNNBL1
    nsv7096025copy number variation1nstd102humanUncertain significance GRCh37 chr20: 35,569,422-36,500,415 , GRCh38.p12 chr20: 36,941,019-37,872,013 RPN2, SAMHD1, 19 more genes
    nsv7067087inversion1nstd229human GRCh38 chr20: 37,795,379-37,801,200 , GRCh37.p13 chr20: 36,423,781-36,429,602 CTNNBL1
    nsv7062736inversion1nstd229human GRCh38 chr20: 36,955,253-45,585,462 , GRCh37.p13 chr20: 35,583,656-44,214,101 GDAP1L1, PI3, 177 more genes
    nsv7059101inversion1nstd229human GRCh38 chr20: 37,692,160-38,740,390 , GRCh37.p13 chr20: 36,320,562-37,369,033 LBP, SNORA71C, 24 more genes
    nsv7038037copy number variation1nstd229human GRCh38 chr20: 37,757,301-37,840,200 , GRCh37.p13 chr20: 36,385,703-36,468,602 CTNNBL1
    nsv7037755copy number variation1nstd229human GRCh38 chr20: 37,712,653-37,712,882 , GRCh37.p13 chr20: 36,341,055-36,341,284 CTNNBL1
    nsv7035864copy number variation1nstd229human GRCh38 chr20: 37,837,194-37,837,566 , GRCh37.p13 chr20: 36,465,596-36,465,968 CTNNBL1
    nsv7035769copy number variation1nstd229human GRCh38 chr20: 37,716,860-37,725,315 , GRCh37.p13 chr20: 36,345,262-36,353,717 CTNNBL1
    nsv7034498copy number variation1nstd229human GRCh38 chr20: 37,143,392-40,581,574 , GRCh37.p13 chr20: 35,771,795-39,210,214 ADIG, TGM2, 61 more genes
    nsv7034450copy number variation1nstd229human GRCh38 chr20: 37,803,940-37,804,216 , GRCh37.p13 chr20: 36,432,342-36,432,618 CTNNBL1
    nsv7030520copy number variation1nstd229human GRCh38 chr20: 37,846,111-37,848,919 , GRCh37.p13 chr20: 36,474,513-36,477,321 CTNNBL1
    nsv7026905copy number variation1nstd229human GRCh38 chr20: 37,806,523-37,816,614 , GRCh37.p13 chr20: 36,434,925-36,445,016 CTNNBL1
    nsv7024720copy number variation1nstd229human GRCh38 chr20: 37,796,301-37,799,100 , GRCh37.p13 chr20: 36,424,703-36,427,502 CTNNBL1
    nsv7024237copy number variation1nstd229human GRCh38 chr20: 37,784,494-37,794,542 , GRCh37.p13 chr20: 36,412,896-36,422,944 CTNNBL1
    nsv7022179copy number variation1nstd229human GRCh38 chr20: 37,841,104-37,847,986 , GRCh37.p13 chr20: 36,469,506-36,476,388 CTNNBL1
    nsv7021879copy number variation1nstd229human GRCh38 chr20: 37,815,142-37,819,568 , GRCh37.p13 chr20: 36,443,544-36,447,970 CTNNBL1
    nsv7021345copy number variation1nstd229human GRCh38 chr20: 37,838,937-37,878,358 , GRCh37.p13 chr20: 36,467,339-36,506,760 CTNNBL1
    nsv7021198copy number variation1nstd229human GRCh38 chr20: 33,145,032-41,995,765 , GRCh37.p13 chr20: 31,732,838-40,624,405 PXMP4, RPL12P11, 199 more genes
    nsv7020768copy number variation1nstd229human GRCh38 chr20: 37,741,367-37,743,215 , GRCh37.p13 chr20: 36,369,769-36,371,617 CTNNBL1
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