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Items: 1 to 20 of 790

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131582insertion1nstd186human GRCh37 chr12: 131,490,145-131,490,163 , GRCh38.p12 chr12: 131,005,600-131,005,618 ADGRD1
    nsv6131575insertion1nstd186human GRCh37 chr12: 131,582,734-131,582,765 , GRCh38.p12 chr12: 131,098,189-131,098,220 ADGRD1
    nsv6121768copy number variation1nstd186human GRCh37 chr12: 131,490,167-131,490,261 , GRCh38.p12 chr12: 131,005,622-131,005,716 ADGRD1
    nsv6120788copy number variation1nstd186human GRCh37 chr12: 131,517,264-131,517,530 , GRCh38.p12 chr12: 131,032,719-131,032,985 ADGRD1
    nsv5974811insertion1nstd209human GRCh38 chr12: 131,098,170-131,098,170 , GRCh37.p13 chr12: 131,582,715-131,582,715 ADGRD1
    nsv5973940insertion1nstd209human GRCh38 chr12: 131,093,946-131,093,946 , GRCh37.p13 chr12: 131,578,491-131,578,491 ADGRD1
    nsv5972721insertion1nstd209human GRCh38 chr12: 131,005,650-131,005,650 , GRCh37.p13 chr12: 131,490,195-131,490,195 ADGRD1
    nsv5944826copy number variation1nstd209human GRCh38 chr12: 131,037,830-131,038,037 , GRCh37.p13 chr12: 131,522,375-131,522,582 ADGRD1
    nsv5944021copy number variation1nstd209human GRCh38 chr12: 131,067,471-131,067,530 , GRCh37.p13 chr12: 131,552,016-131,552,075 ADGRD1
    nsv5942933copy number variation1nstd209human GRCh38 chr12: 131,029,480-131,030,278 , GRCh37.p13 chr12: 131,514,025-131,514,823 ADGRD1
    nsv5942828copy number variation1nstd209human GRCh38 chr12: 131,037,084-131,037,346 , GRCh37.p13 chr12: 131,521,629-131,521,891 ADGRD1
    nsv5942808copy number variation1nstd209human GRCh38 chr12: 131,036,275-131,036,491 , GRCh37.p13 chr12: 131,520,820-131,521,036 ADGRD1
    nsv5942470copy number variation1nstd209human GRCh38 chr12: 131,032,719-131,032,984 , GRCh37.p13 chr12: 131,517,264-131,517,529 ADGRD1
    nsv5936160copy number variation1nstd209human GRCh38 chr12: 131,045,976-131,046,174 , GRCh37.p13 chr12: 131,530,521-131,530,719 ADGRD1
    nsv5933827copy number variation1nstd209human GRCh38 chr12: 131,104,223-131,104,289 , GRCh37.p13 chr12: 131,588,768-131,588,834 ADGRD1
    nsv5929543copy number variation1nstd209human GRCh38 chr12: 131,039,231-131,039,351 , GRCh37.p13 chr12: 131,523,776-131,523,896 ADGRD1
    nsv5928354copy number variation1nstd209human GRCh38 chr12: 131,096,002-131,096,052 , GRCh37.p13 chr12: 131,580,547-131,580,597 ADGRD1
    nsv5718365mobile element insertion1nstd211human GRCh38 chr12: 130,967,553-130,967,553 , GRCh37.p13 chr12: 131,452,098-131,452,098 ADGRD1
    nsv5714291mobile element insertion2nstd211human GRCh38 chr12: 130,963,742-130,963,742 , GRCh37.p13 chr12: 131,448,287-131,448,287 ADGRD1
    nsv5708464mobile element insertion1nstd211human GRCh38 chr12: 131,106,635-131,106,635 , GRCh37.p13 chr12: 131,591,180-131,591,180 ADGRD1
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