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Items: 1 to 20 of 549

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5959067insertion1nstd209human GRCh38 chr2: 240,527,763-240,527,763 , GRCh37.p13 chr2: 241,467,180-241,467,180 ANKMY1
    nsv5901701copy number variation1nstd209human GRCh38 chr2: 240,472,210-240,472,277 , GRCh37.p13 chr2: 241,411,627-241,411,694 ANKMY1
    nsv5895837copy number variation1nstd209human GRCh38 chr2: 240,508,886-240,509,240 , GRCh37.p13 chr2: 241,448,303-241,448,657 ANKMY1
    nsv5718816mobile element insertion2nstd211human GRCh38 chr2: 240,487,611-240,487,611 , GRCh37.p13 chr2: 241,427,028-241,427,028 ANKMY1
    nsv5688190mobile element insertion1nstd211human GRCh38 chr2: 240,516,163-240,516,163 , GRCh37.p13 chr2: 241,455,580-241,455,580 ANKMY1
    nsv5616015insertion1nstd207human GRCh38 chr2: 240,527,763-240,527,763 , GRCh37.p13 chr2: 241,467,180-241,467,180 ANKMY1
    nsv5615656insertion1nstd207human GRCh38 chr2: 240,472,226-240,472,226 , GRCh37.p13 chr2: 241,411,643-241,411,643 ANKMY1
    nsv5612563insertion1nstd207human GRCh38 chr2: 240,527,128-240,527,128 , GRCh37.p13 chr2: 241,466,545-241,466,545 ANKMY1
    nsv5570226copy number variation1nstd207human GRCh38 chr2: 240,498,469-240,498,537 , GRCh37.p13 chr2: 241,437,886-241,437,954 ANKMY1
    nsv5450595copy number variation1nstd206human GRCh38 chr2: 240,526,742-240,527,626 , GRCh37.p13 chr2: 241,466,159-241,467,043 ANKMY1
    nsv5449468copy number variation1nstd206human GRCh38 chr2: 240,517,614-240,517,677 , GRCh37.p13 chr2: 241,457,031-241,457,094 ANKMY1
    nsv5449293copy number variation1nstd206human GRCh38 chr2: 240,542,866-240,542,923 , GRCh37.p13 chr2: 241,482,283-241,482,340 ANKMY1
    nsv5447533copy number variation1nstd206human GRCh38 chr2: 240,487,835-240,574,804 , GRCh37.p13 chr2: 241,427,252-241,514,221 DUSP28, RNPEPL1, 1 more genes
    nsv5441507copy number variation1nstd206human GRCh38 chr2: 240,527,292-240,527,597 , GRCh37.p13 chr2: 241,466,709-241,467,014 ANKMY1
    nsv5436879copy number variation1nstd206human GRCh38 chr2: 240,534,706-240,534,770 , GRCh37.p13 chr2: 241,474,123-241,474,187 ANKMY1
    nsv5435839copy number variation1nstd206human GRCh38 chr2: 240,538,663-240,539,254 , GRCh37.p13 chr2: 241,478,080-241,478,671 ANKMY1
    nsv5381323copy number variation1nstd102humanPathogenic GRCh37 chr2: 237,201,756-243,048,760 , GRCh38.p12 chr2: 236,293,113-242,106,609 LRRFIP1, GPR35, 133 more genes
    nsv5366917translocation1nstd200human GRCh38 chr2: 240,476,217-240,476,217 , GRCh38 chr2: 240,474,052-240,474,052 , GRCh37.p13 chr2: 241,415,634-241,415,634 , GRCh37.p13 chr2: 241,413,469-241,413,469 ANKMY1
    nsv5366916translocation1nstd200human GRCh38 chr2: 240,476,468-240,476,468 , GRCh38 chr2: 240,474,047-240,474,047 , GRCh37.p13 chr2: 241,413,464-241,413,464 , GRCh37.p13 chr2: 241,415,885-241,415,885 ANKMY1
    nsv5351288translocation1nstd200human GRCh38 chr2: 240,538,663-240,538,663 , GRCh38 chr2: 240,539,254-240,539,254 , GRCh37.p13 chr2: 241,478,080-241,478,080 , GRCh37.p13 chr2: 241,478,671-241,478,671 ANKMY1
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