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Items: 1 to 20 of 312

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5959642insertion1nstd209human GRCh38 chr6: 99,933,015-99,933,015 , GRCh37.p13 chr6: 100,380,891-100,380,891 MCHR2
    nsv5950572insertion1nstd209human GRCh38 chr6: 99,959,609-99,959,609 , GRCh37.p13 chr6: 100,407,485-100,407,485 MCHR2
    nsv5692677mobile element insertion1nstd211human GRCh38 chr6: 99,936,886-99,936,886 , GRCh37.p13 chr6: 100,384,762-100,384,762 MCHR2
    nsv5688642mobile element insertion2nstd211human GRCh38 chr6: 99,933,031-99,933,031 , GRCh37.p13 chr6: 100,380,907-100,380,907 MCHR2
    nsv5687279mobile element insertion2nstd211human GRCh38 chr6: 99,959,623-99,959,623 , GRCh37.p13 chr6: 100,407,499-100,407,499 MCHR2
    nsv5637116insertion1nstd207human GRCh38 chr6: 99,933,015-99,933,015 , GRCh37.p13 chr6: 100,380,891-100,380,891 MCHR2
    nsv5627315insertion1nstd207human GRCh38 chr6: 99,959,609-99,959,609 , GRCh37.p13 chr6: 100,407,485-100,407,485 MCHR2
    nsv5464627copy number variation1nstd206human GRCh38 chr6: 99,956,420-99,959,902 , GRCh37.p13 chr6: 100,404,296-100,407,778 MCHR2
    nsv5463853copy number variation1nstd206human GRCh38 chr6: 99,956,551-99,962,758 , GRCh37.p13 chr6: 100,404,427-100,410,634 MCHR2
    nsv5456242copy number variation1nstd206human GRCh38 chr6: 99,899,220-99,945,068 , GRCh37.p13 chr6: 100,347,096-100,392,944 MCHR2
    nsv5407716mobile element insertion1nstd206human GRCh38 chr6: 99,933,031-99,933,082 , GRCh37.p13 chr6: 100,380,907-100,380,958 MCHR2
    nsv5398474mobile element insertion1nstd206human GRCh38 chr6: 99,959,609-99,959,609 , GRCh37.p13 chr6: 100,407,485-100,407,485 MCHR2
    nsv5363271translocation1nstd200human GRCh38 chr6: 99,990,830-99,990,830 , GRCh38 chr6: 99,990,918-99,990,918 , GRCh37.p13 chr6: 100,438,706-100,438,706 , GRCh37.p13 chr6: 100,438,794-100,438,794 MCHR2
    nsv5363270translocation1nstd200human GRCh38 chr6: 99,921,724-99,921,724 , GRCh38 chr15: 24,763,241-24,763,241 , GRCh37.p13 chr15: 25,008,388-25,008,388 , GRCh37.p13 chr6: 100,369,600-100,369,600 MCHR2
    nsv5363269translocation1nstd200human GRCh38 chr15: 24,763,343-24,763,343 , GRCh38 chr6: 99,921,688-99,921,688 , GRCh37.p13 chr15: 25,008,490-25,008,490 , GRCh37.p13 chr6: 100,369,564-100,369,564 MCHR2
    nsv5344081translocation1nstd200human GRCh37 chr15: 25,008,490-25,008,490 , GRCh37 chr6: 100,369,564-100,369,564 , GRCh38.p12 chr15: 24,763,343-24,763,343 , GRCh38.p12 chr6: 99,921,688-99,921,688 MCHR2
    nsv5332943translocation1nstd200human GRCh37 chr15: 25,008,388-25,008,388 , GRCh37 chr6: 100,369,600-100,369,600 , GRCh38.p12 chr15: 24,763,241-24,763,241 , GRCh38.p12 chr6: 99,921,724-99,921,724 MCHR2
    nsv5323176translocation1nstd204human GRCh38.p13 chr6: 99,921,724-99,921,724 , GRCh38.p13 chr15: 24,763,241-24,763,241 , GRCh37.p13 chr15: 25,008,388-25,008,388 , GRCh37.p13 chr6: 100,369,600-100,369,600 MCHR2
    nsv5322269translocation1nstd204human GRCh38.p13 chr6: 99,921,688-99,921,688 , GRCh38.p13 chr15: 24,763,343-24,763,343 , GRCh37.p13 chr15: 25,008,490-25,008,490 , GRCh37.p13 chr6: 100,369,564-100,369,564 MCHR2
    nsv5230101copy number variation1nstd204human GRCh38.p13 chr6: 99,927,722-99,931,280 , GRCh37.p13 chr6: 100,375,598-100,379,156 MCHR2
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