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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5901525copy number variation1nstd209human GRCh38 chr2: 190,238,324-190,238,686 , GRCh37.p13 chr2: 191,103,050-191,103,412 HIBCH
    nsv5888177copy number variation1nstd209human GRCh38 chr2: 190,263,802-190,263,892 , GRCh37.p13 chr2: 191,128,528-191,128,618 HIBCH
    nsv5692947mobile element insertion1nstd211human GRCh38 chr2: 190,314,321-190,314,321 , GRCh37.p13 chr2: 191,179,047-191,179,047 HIBCH
    nsv5684381mobile element insertion1nstd211human GRCh38 chr2: 190,252,877-190,252,877 , GRCh37.p13 chr2: 191,117,603-191,117,603 HIBCH
    nsv5683064mobile element insertion1nstd211human GRCh38 chr2: 190,284,922-190,284,922 , GRCh37.p13 chr2: 191,149,648-191,149,648 HIBCH
    nsv5681840mobile element insertion1nstd211human GRCh38 chr2: 190,273,704-190,273,704 , GRCh37.p13 chr2: 191,138,430-191,138,430 HIBCH
    nsv5676168mobile element insertion1nstd211human GRCh38 chr2: 190,297,858-190,297,858 , GRCh37.p13 chr2: 191,162,584-191,162,584 HIBCH
    nsv5617561insertion1nstd207human GRCh38 chr2: 190,256,472-190,256,472 , GRCh37.p13 chr2: 191,121,198-191,121,198 HIBCH
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5449015copy number variation1nstd206human GRCh38 chr2: 190,276,671-190,280,595 , GRCh37.p13 chr2: 191,141,397-191,145,321 HIBCH
    nsv5411445mobile element insertion1nstd206human GRCh38 chr2: 190,252,877-190,252,928 , GRCh37.p13 chr2: 191,117,603-191,117,654 HIBCH
    nsv5407699mobile element insertion1nstd206human GRCh38 chr2: 190,297,858-190,297,909 , GRCh37.p13 chr2: 191,162,584-191,162,635 HIBCH
    nsv5399589mobile element insertion1nstd206human GRCh38 chr2: 190,284,922-190,284,973 , GRCh37.p13 chr2: 191,149,648-191,149,699 HIBCH
    nsv5361154translocation1nstd200human GRCh38 chr2: 190,267,638-190,267,638 , GRCh38 chr2: 190,267,401-190,267,401 , GRCh37.p13 chr2: 191,132,127-191,132,127 , GRCh37.p13 chr2: 191,132,364-191,132,364 HIBCH
    nsv5318932copy number variation1nstd204human GRCh38.p13 chr2: 190,280,806-190,281,027 , GRCh37.p13 chr2: 191,145,532-191,145,753 HIBCH
    nsv5315701copy number variation1nstd204human GRCh38.p13 chr2: 190,267,394-190,267,642 , GRCh37.p13 chr2: 191,132,120-191,132,368 HIBCH
    nsv5305336copy number variation1nstd204human GRCh38.p13 chr2: 190,309,088-190,318,360 , GRCh37.p13 chr2: 191,173,814-191,183,086 HIBCH
    nsv5211009copy number variation1nstd204human GRCh38.p13 chr2: 190,308,703-190,309,902 , GRCh37.p13 chr2: 191,173,429-191,174,628 HIBCH
    nsv5205527copy number variation1nstd204human GRCh38.p13 chr2: 190,308,741-190,318,515 , GRCh37.p13 chr2: 191,173,467-191,183,241 HIBCH
    nsv5200844copy number variation1nstd204human GRCh38.p13 chr2: 190,309,503-190,310,702 , GRCh37.p13 chr2: 191,174,229-191,175,428 HIBCH
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