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Items: 1 to 20 of 583

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5975097insertion1nstd209human GRCh38 chr22: 34,034,609-34,034,609 , GRCh37.p13 chr22: 34,430,598-34,430,598 LINC01643
    nsv5963174copy number variation1nstd209human GRCh38 chr22: 34,157,738-34,157,835 , GRCh37.p13 chr22: 34,553,727-34,553,824 LINC01643
    nsv5961907copy number variation1nstd209human GRCh38 chr22: 34,141,561-34,152,325 , GRCh37.p13 chr22: 34,537,550-34,548,314 LINC01643
    nsv5885091copy number variation1nstd209human GRCh38 chr22: 34,141,567-34,151,409 , GRCh37.p13 chr22: 34,537,556-34,547,398 LINC01643
    nsv5719004mobile element insertion2nstd211human GRCh38 chr22: 34,084,759-34,084,759 , GRCh37.p13 chr22: 34,480,748-34,480,748 LINC01643
    nsv5710548mobile element insertion1nstd211human GRCh38 chr22: 34,031,983-34,031,983 , GRCh37.p13 chr22: 34,427,972-34,427,972 LINC01643
    nsv5705877mobile element insertion2nstd211human GRCh38 chr22: 34,034,623-34,034,623 , GRCh37.p13 chr22: 34,430,612-34,430,612 LINC01643
    nsv5703438mobile element insertion1nstd211human GRCh38 chr22: 34,099,102-34,099,102 , GRCh37.p13 chr22: 34,495,091-34,495,091 LINC01643
    nsv5697923mobile element insertion2nstd211human GRCh38 chr22: 34,062,529-34,062,529 , GRCh37.p13 chr22: 34,458,518-34,458,518 LINC01643
    nsv5694496mobile element insertion1nstd211human GRCh38 chr22: 34,164,010-34,164,010 , GRCh37.p13 chr22: 34,559,999-34,559,999 LINC01643
    nsv5671802insertion1nstd207human GRCh38 chr22: 34,138,433-34,138,433 , GRCh37.p13 chr22: 34,534,422-34,534,422 LINC01643
    nsv5671091insertion1nstd207human GRCh38 chr22: 34,132,594-34,132,594 , GRCh37.p13 chr22: 34,528,583-34,528,583 LINC01643
    nsv5669627insertion1nstd207human GRCh38 chr22: 34,034,609-34,034,609 , GRCh37.p13 chr22: 34,430,598-34,430,598 LINC01643
    nsv5600741copy number variation1nstd207human GRCh38 chr22: 34,157,738-34,157,835 , GRCh37.p13 chr22: 34,553,727-34,553,824 LINC01643
    nsv5561701mobile element insertion1nstd206human GRCh38 chr22: 34,084,759-34,084,810 , GRCh37.p13 chr22: 34,480,748-34,480,799 LINC01643
    nsv5553215copy number variation1nstd206human GRCh38 chr22: 34,152,066-34,152,272 , GRCh37.p13 chr22: 34,548,055-34,548,261 LINC01643
    nsv5546585copy number variation1nstd206human GRCh38 chr22: 34,159,862-34,186,264 , GRCh37.p13 chr22: 34,555,851-34,582,253 LINC01643
    nsv5543709copy number variation1nstd206human GRCh38 chr22: 34,173,770-34,177,004 , GRCh37.p13 chr22: 34,569,759-34,572,993 LINC01643
    nsv5542712copy number variation1nstd206human GRCh38 chr22: 34,061,196-34,067,161 , GRCh37.p13 chr22: 34,457,185-34,463,150 LINC01643
    nsv5432544mobile element insertion1nstd206human GRCh38 chr22: 34,164,010-34,164,061 , GRCh37.p13 chr22: 34,559,999-34,560,050 LINC01643
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