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Items: 1 to 20 of 1077

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5962644insertion1nstd209human GRCh38 chr4: 30,974,246-30,974,246 , GRCh37.p13 chr4: 30,975,868-30,975,868 PCDH7
    nsv5961238insertion1nstd209human GRCh38 chr4: 30,924,539-30,924,539 , GRCh37.p13 chr4: 30,926,161-30,926,161 PCDH7
    nsv5953185insertion1nstd209human GRCh38 chr4: 30,890,444-30,890,444 , GRCh37.p13 chr4: 30,892,066-30,892,066 PCDH7
    nsv5951770insertion1nstd209human GRCh38 chr4: 31,074,784-31,074,784 , GRCh37.p13 chr4: 31,076,406-31,076,406 PCDH7
    nsv5950613insertion1nstd209human GRCh38 chr4: 30,739,160-30,739,160 , GRCh37.p13 chr4: 30,740,782-30,740,782 PCDH7
    nsv5903946copy number variation1nstd209human GRCh38 chr4: 31,012,325-31,013,349 , GRCh37.p13 chr4: 31,013,947-31,014,971 PCDH7
    nsv5897419copy number variation1nstd209human GRCh38 chr4: 30,959,001-30,959,637 , GRCh37.p13 chr4: 30,960,623-30,961,259 PCDH7
    nsv5895484copy number variation1nstd209human GRCh38 chr4: 30,968,173-30,968,406 , GRCh37.p13 chr4: 30,969,795-30,970,028 PCDH7
    nsv5893524copy number variation1nstd209human GRCh38 chr4: 30,756,138-30,760,890 , GRCh37.p13 chr4: 30,757,760-30,762,512 PCDH7
    nsv5892185copy number variation1nstd209human GRCh38 chr4: 30,977,004-30,987,574 , GRCh37.p13 chr4: 30,978,626-30,989,196 PCDH7
    nsv5890448copy number variation1nstd209human GRCh38 chr4: 31,088,856-31,089,002 , GRCh37.p13 chr4: 31,090,478-31,090,624 PCDH7
    nsv5889204copy number variation1nstd209human GRCh38 chr4: 31,132,576-31,132,730 , GRCh37.p13 chr4: 31,134,198-31,134,352 PCDH7
    nsv5888519copy number variation1nstd209human GRCh38 chr4: 31,096,852-31,097,079 , GRCh37.p13 chr4: 31,098,474-31,098,701 PCDH7
    nsv5839535copy number variation1nstd209human GRCh38 chr4: 31,139,124-31,140,323 , GRCh37.p13 chr4: 31,140,746-31,141,945 PCDH7
    nsv5838981copy number variation1nstd209human GRCh38 chr4: 30,977,394-30,987,173 , GRCh37.p13 chr4: 30,979,016-30,988,795 PCDH7
    nsv5838980copy number variation1nstd209human GRCh38 chr4: 30,755,967-30,760,374 , GRCh37.p13 chr4: 30,757,589-30,761,996 PCDH7
    nsv5730242mobile element insertion1nstd211human GRCh38 chr4: 30,986,396-30,986,396 , GRCh37.p13 chr4: 30,988,018-30,988,018 PCDH7
    nsv5721729mobile element insertion1nstd211human GRCh38 chr4: 30,929,678-30,929,678 , GRCh37.p13 chr4: 30,931,300-30,931,300 PCDH7
    nsv5714801mobile element insertion1nstd211human GRCh38 chr4: 30,929,516-30,929,516 , GRCh37.p13 chr4: 30,931,138-30,931,138 PCDH7
    nsv5694080mobile element insertion2nstd211human GRCh38 chr4: 30,921,811-30,921,811 , GRCh37.p13 chr4: 30,923,433-30,923,433 PCDH7
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