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Items: 1 to 20 of 1858

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6124430insertion1nstd186human GRCh37 chr2: 77,068,238-77,068,273 , GRCh38.p12 chr2: 76,841,112-76,841,147 LRRTM4
    nsv5973694inversion1nstd209human GRCh38 chr2: 76,823,957-76,824,603 , GRCh37.p13 chr2: 77,051,083-77,051,729 LRRTM4
    nsv5972728inversion1nstd209human GRCh38 chr2: 76,824,604-76,825,551 , GRCh37.p13 chr2: 77,051,730-77,052,677 LRRTM4
    nsv5969526inversion1nstd209human GRCh38 chr2: 77,300,182-77,300,427 , GRCh37.p13 chr2: 77,527,308-77,527,553 LRRTM4
    nsv5964727insertion1nstd209human GRCh38 chr2: 77,362,170-77,362,170 , GRCh37.p13 chr2: 77,589,296-77,589,296 LRRTM4
    nsv5962564insertion1nstd209human GRCh38 chr2: 77,217,377-77,217,377 , GRCh37.p13 chr2: 77,444,503-77,444,503 LRRTM4
    nsv5959564insertion1nstd209human GRCh38 chr2: 76,986,282-76,986,282 , GRCh37.p13 chr2: 77,213,408-77,213,408 LRRTM4, LRRTM4-AS1
    nsv5956671insertion1nstd209human GRCh38 chr2: 77,089,239-77,089,239 , GRCh37.p13 chr2: 77,316,365-77,316,365 LRRTM4
    nsv5955297insertion1nstd209human GRCh38 chr2: 76,873,506-76,873,506 , GRCh37.p13 chr2: 77,100,632-77,100,632 LRRTM4
    nsv5954590insertion1nstd209human GRCh38 chr2: 77,313,390-77,313,390 , GRCh37.p13 chr2: 77,540,516-77,540,516 LRRTM4
    nsv5952187insertion1nstd209human GRCh38 chr2: 77,068,907-77,068,907 , GRCh37.p13 chr2: 77,296,033-77,296,033 LRRTM4
    nsv5886085copy number variation1nstd209human GRCh38 chr2: 77,092,974-77,093,997 , GRCh37.p13 chr2: 77,320,100-77,321,123 LRRTM4
    nsv5885588copy number variation1nstd209human GRCh38 chr2: 77,062,220-77,063,007 , GRCh37.p13 chr2: 77,289,346-77,290,133 LRRTM4
    nsv5885232copy number variation1nstd209human GRCh38 chr2: 76,892,867-76,893,647 , GRCh37.p13 chr2: 77,119,993-77,120,773 LRRTM4
    nsv5883800copy number variation1nstd209human GRCh38 chr2: 77,336,168-77,336,228 , GRCh37.p13 chr2: 77,563,294-77,563,354 LRRTM4
    nsv5882685copy number variation1nstd209human GRCh38 chr2: 77,136,713-77,137,510 , GRCh37.p13 chr2: 77,363,839-77,364,636 LRRTM4
    nsv5882074copy number variation1nstd209human GRCh38 chr2: 76,746,201-76,746,294 , GRCh37.p13 chr2: 76,973,327-76,973,420 LRRTM4
    nsv5881328copy number variation1nstd209human GRCh38 chr2: 77,099,594-77,099,822 , GRCh37.p13 chr2: 77,326,720-77,326,948 LRRTM4
    nsv5881123copy number variation1nstd209human GRCh38 chr2: 77,313,433-77,313,509 , GRCh37.p13 chr2: 77,540,559-77,540,635 LRRTM4
    nsv5880321copy number variation1nstd209human GRCh38 chr2: 76,774,321-76,774,453 , GRCh37.p13 chr2: 77,001,447-77,001,579 LRRTM4
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