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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5893677copy number variation1nstd209human GRCh38 chr2: 190,496,683-190,496,758 , GRCh37.p13 chr2: 191,361,409-191,361,484 MFSD6, NEMP2
    nsv5888904copy number variation1nstd209human GRCh38 chr2: 190,457,044-190,464,323 , GRCh37.p13 chr2: 191,321,770-191,329,049 NEMP2, MFSD6
    nsv5832099copy number variation1nstd209human GRCh38 chr2: 190,457,136-190,464,385 , GRCh37.p13 chr2: 191,321,862-191,329,111 NEMP2, MFSD6
    nsv5693682mobile element insertion1nstd211human GRCh38 chr2: 190,592,659-190,592,659 , GRCh37.p13 chr2: 191,457,385-191,457,385 NEMP2
    nsv5691226mobile element insertion1nstd211human GRCh38 chr2: 190,603,875-190,603,875 , GRCh37.p13 chr2: 191,468,601-191,468,601 NEMP2
    nsv5677411mobile element insertion1nstd211human GRCh38 chr2: 190,492,138-190,492,138 , GRCh37.p13 chr2: 191,356,864-191,356,864 NEMP2, MFSD6
    nsv5676202mobile element insertion2nstd211human GRCh38 chr2: 190,479,524-190,479,524 , GRCh37.p13 chr2: 191,344,250-191,344,250 NEMP2, MFSD6
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5541653insertion1nstd206human GRCh38 chr2: 190,479,524-190,479,575 , GRCh37.p13 chr2: 191,344,250-191,344,301 MFSD6, NEMP2
    nsv5452529copy number variation1nstd206human GRCh38 chr2: 190,455,203-190,455,969 , GRCh37.p13 chr2: 191,319,929-191,320,695 MFSD6, NEMP2
    nsv5441678copy number variation1nstd206human GRCh38 chr2: 190,534,847-190,534,917 , GRCh37.p13 chr2: 191,399,573-191,399,643 NEMP2, NEMP2-DT
    nsv5433975copy number variation1nstd206human GRCh38 chr2: 190,594,922-190,596,027 , GRCh37.p13 chr2: 191,459,648-191,460,753 NEMP2
    nsv5403259mobile element insertion1nstd206human GRCh38 chr2: 190,592,659-190,592,710 , GRCh37.p13 chr2: 191,457,385-191,457,436 NEMP2
    nsv5400622mobile element insertion1nstd206human GRCh38 chr2: 190,603,875-190,603,926 , GRCh37.p13 chr2: 191,468,601-191,468,652 NEMP2
    nsv5332436translocation1nstd200human GRCh37 chr2: 191,401,021-191,401,021 , GRCh37 chr4: 143,904,989-143,904,989 , GRCh38.p12 chr2: 190,536,295-190,536,295 , GRCh38.p12 chr4: 142,983,836-142,983,836 , NEMP2, 1 more genes
    nsv5303891copy number variation1nstd204human GRCh38.p13 chr2: 190,484,567-190,515,909 , GRCh37.p13 chr2: 191,349,293-191,380,635 MFSD6, NEMP2
    nsv5218523copy number variation1nstd204human GRCh38.p13 chr2: 190,488,243-190,490,275 , GRCh37.p13 chr2: 191,352,969-191,355,001 MFSD6, NEMP2
    nsv5217636copy number variation1nstd204human GRCh38.p13 chr2: 190,482,514-190,507,324 , GRCh37.p13 chr2: 191,347,240-191,372,050 NEMP2, MFSD6
    nsv5208984copy number variation1nstd204human GRCh38.p13 chr2: 190,484,501-190,511,600 , GRCh37.p13 chr2: 191,349,227-191,376,326 MFSD6, NEMP2
    nsv5201967copy number variation1nstd204human GRCh38.p13 chr2: 190,512,301-190,515,900 , GRCh37.p13 chr2: 191,377,027-191,380,626 NEMP2
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