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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5904873copy number variation1nstd209human GRCh38 chr6: 47,002,764-47,004,564 , GRCh37.p13 chr6: 46,970,501-46,972,301 ADGRF1
    nsv5897355copy number variation1nstd209human GRCh38 chr6: 47,012,975-47,015,938 , GRCh37.p13 chr6: 46,980,711-46,983,674 ADGRF1
    nsv5895550copy number variation1nstd209human GRCh38 chr6: 47,019,885-47,023,407 , GRCh37.p13 chr6: 46,987,621-46,991,143 ADGRF1
    nsv5892142copy number variation1nstd209human GRCh38 chr6: 47,023,495-47,023,973 , GRCh37.p13 chr6: 46,991,231-46,991,709 ADGRF1
    nsv5890636copy number variation1nstd209human GRCh38 chr6: 47,019,886-47,023,969 , GRCh37.p13 chr6: 46,987,622-46,991,705 ADGRF1
    nsv5845622copy number variation1nstd209human GRCh38 chr6: 47,012,880-47,015,985 , GRCh37.p13 chr6: 46,980,616-46,983,721 ADGRF1
    nsv5844979copy number variation2nstd209human GRCh38 chr6: 47,021,820-47,023,019 , GRCh37.p13 chr6: 46,989,556-46,990,755 ADGRF1
    nsv5844978copy number variation1nstd209human GRCh38 chr6: 47,020,282-47,024,019 , GRCh37.p13 chr6: 46,988,018-46,991,755 ADGRF1
    nsv5844977copy number variation1nstd209human GRCh38 chr6: 47,002,730-47,004,629 , GRCh37.p13 chr6: 46,970,467-46,972,366 ADGRF1
    nsv5726090mobile element insertion1nstd211human GRCh38 chr6: 47,021,378-47,021,378 , GRCh37.p13 chr6: 46,989,114-46,989,114 ADGRF1
    nsv5721013mobile element insertion1nstd211human GRCh38 chr6: 47,021,353-47,021,353 , GRCh37.p13 chr6: 46,989,089-46,989,089 ADGRF1
    nsv5561908mobile element insertion1nstd206human GRCh38 chr6: 47,021,378-47,021,429 , GRCh37.p13 chr6: 46,989,114-46,989,165 ADGRF1
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5468561copy number variation1nstd206human GRCh38 chr6: 47,009,478-47,009,554 , GRCh37.p13 chr6: 46,977,214-46,977,290 ADGRF1
    nsv5462975copy number variation1nstd206human GRCh38 chr6: 47,002,766-47,004,565 , GRCh37.p13 chr6: 46,970,503-46,972,302 ADGRF1
    nsv5160692mobile element insertion1nstd203human GRCh38 chr6: 47,000,403-47,000,421 , GRCh37.p13 chr6: 46,968,140-46,968,158 ADGRF1
    nsv4941253copy number variation1nstd200human GRCh38 chr6: 47,035,577-47,035,678 , GRCh37.p13 chr6: 47,003,313-47,003,414 ADGRF1
    nsv4941252copy number variation1nstd200human GRCh38 chr6: 47,002,766-47,004,565 , GRCh37.p13 chr6: 46,970,503-46,972,302 ADGRF1
    nsv4941251copy number variation1nstd200human GRCh38 chr6: 46,999,349-46,999,511 , GRCh37.p13 chr6: 46,967,086-46,967,248 ADGRF1
    nsv4934706copy number variation1nstd200human GRCh38 chr6: 47,015,611-47,021,413 , GRCh37.p13 chr6: 46,983,347-46,989,149 ADGRF1
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