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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5925874copy number variation1nstd209human GRCh38 chr12: 14,410,611-14,410,691 , GRCh37.p13 chr12: 14,563,545-14,563,625 ATF7IP
    nsv5918157copy number variation1nstd209human GRCh38 chr12: 14,487,135-14,493,115 , GRCh37.p13 chr12: 14,640,069-14,646,049 ATF7IP
    nsv5866174copy number variation1nstd209human GRCh38 chr12: 14,461,360-14,466,366 , GRCh37.p13 chr12: 14,614,294-14,619,300 ATF7IP
    nsv5865836copy number variation1nstd209human GRCh38 chr12: 14,499,787-14,529,533 , GRCh37.p13 chr12: 14,652,721-14,682,467 PLBD1, ATF7IP, 1 more genes
    nsv5865714copy number variation1nstd209human GRCh38 chr12: 14,462,160-14,471,674 , GRCh37.p13 chr12: 14,615,094-14,624,608 ATF7IP
    nsv5864066copy number variation1nstd209human GRCh38 chr12: 14,484,858-14,493,236 , GRCh37.p13 chr12: 14,637,792-14,646,170 ATF7IP
    nsv5857285copy number variation1nstd209human GRCh38 chr12: 14,471,775-14,497,734 , GRCh37.p13 chr12: 14,624,709-14,650,668 ATF7IP
    nsv5853374copy number variation1nstd209human GRCh38 chr12: 14,503,142-14,505,859 , GRCh37.p13 chr12: 14,656,076-14,658,793 PLBD1, ATF7IP
    nsv5853294copy number variation1nstd209human GRCh38 chr12: 14,496,935-14,499,886 , GRCh37.p13 chr12: 14,649,869-14,652,820 ATF7IP
    nsv5853276copy number variation1nstd209human GRCh38 chr12: 14,398,532-14,400,831 , GRCh37.p13 chr12: 14,551,466-14,553,765 ATF7IP
    nsv5851493copy number variation1nstd209human GRCh38 chr12: 14,469,394-14,474,515 , GRCh37.p13 chr12: 14,622,328-14,627,449 ATF7IP
    nsv5723184mobile element insertion2nstd211human GRCh38 chr12: 14,374,988-14,374,988 , GRCh37.p13 chr12: 14,527,922-14,527,922 ATF7IP
    nsv5701742mobile element insertion1nstd211human GRCh38 chr12: 14,407,864-14,407,864 , GRCh37.p13 chr12: 14,560,798-14,560,798 ATF7IP
    nsv5701669mobile element insertion1nstd211human GRCh38 chr12: 14,446,970-14,446,970 , GRCh37.p13 chr12: 14,599,904-14,599,904 ATF7IP
    nsv5701276mobile element insertion2nstd211human GRCh38 chr12: 14,372,352-14,372,352 , GRCh37.p13 chr12: 14,525,286-14,525,286 ATF7IP
    nsv5697092mobile element insertion1nstd211human GRCh38 chr12: 14,400,011-14,400,011 , GRCh37.p13 chr12: 14,552,945-14,552,945 ATF7IP
    nsv5559154mobile element insertion1nstd206human GRCh38 chr12: 14,374,988-14,374,993 , GRCh37.p13 chr12: 14,527,922-14,527,927 ATF7IP
    nsv5498312copy number variation1nstd206human GRCh38 chr12: 14,470,737-14,471,990 , GRCh37.p13 chr12: 14,623,671-14,624,924 ATF7IP
    nsv5429623mobile element insertion1nstd206human GRCh38 chr12: 14,372,352-14,372,373 , GRCh37.p13 chr12: 14,525,286-14,525,307 ATF7IP
    nsv5424337mobile element insertion1nstd206human GRCh38 chr12: 14,407,864-14,407,915 , GRCh37.p13 chr12: 14,560,798-14,560,849 ATF7IP
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