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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5906439copy number variation1nstd209human GRCh38 chr2: 148,934,175-148,934,455 , GRCh37.p13 chr2: 149,790,689-149,790,969 KIF5C
    nsv5899442copy number variation1nstd209human GRCh38 chr2: 148,881,719-148,881,849 , GRCh37.p13 chr2: 149,639,288-149,639,418 KIF5C, KIF5C-AS1
    nsv5717953mobile element insertion1nstd211human GRCh38 chr2: 149,023,832-149,023,832 , GRCh37.p13 chr2: 149,880,346-149,880,346 KIF5C
    nsv5676472mobile element insertion2nstd211human GRCh38 chr2: 148,918,131-148,918,131 , GRCh37.p13 chr2: 149,675,700-149,675,700 KIF5C, LOC101928553
    nsv5614042insertion1nstd207human GRCh38 chr2: 148,957,970-148,957,970 , GRCh37.p13 chr2: 149,814,484-149,814,484 KIF5C
    nsv5569122copy number variation1nstd207human GRCh38 chr2: 148,881,718-148,881,849 , GRCh37.p13 chr2: 149,639,287-149,639,418 KIF5C, KIF5C-AS1
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5453898copy number variation1nstd206human GRCh38 chr2: 148,881,719-148,881,852 , GRCh37.p13 chr2: 149,639,288-149,639,421 KIF5C, KIF5C-AS1
    nsv5452722copy number variation1nstd206human GRCh38 chr2: 149,017,926-149,022,254 , GRCh37.p13 chr2: 149,874,440-149,878,768 KIF5C
    nsv5450895copy number variation1nstd206human GRCh38 chr2: 141,459,078-156,842,302 , GRCh37.p13 chr2: 142,216,647-157,698,814 , LOC105373696, 163 more genes
    nsv5440002copy number variation1nstd206human GRCh38 chr2: 148,915,544-148,915,666 , GRCh37.p13 chr2: 149,673,113-149,673,235 KIF5C, LOC101928553
    nsv5438106copy number variation1nstd206human GRCh38 chr2: 149,002,936-149,002,989 , GRCh37.p13 chr2: 149,859,450-149,859,503 KIF5C
    nsv5434730copy number variation1nstd206human GRCh38 chr2: 148,693,148-164,933,481 , GRCh37.p13 chr2: 149,450,717-165,789,991 , RBM43, 205 more genes
    nsv5402216mobile element insertion1nstd206human GRCh38 chr2: 148,918,131-148,918,182 , GRCh37.p13 chr2: 149,675,700-149,675,751 LOC101928553, KIF5C
    nsv5381338copy number variation1nstd102humanPathogenic GRCh37 chr2: 136,473,383-152,727,396 , GRCh38.p12 chr2: 135,715,813-151,870,882 YY1P2, SPOPL, 156 more genes
    nsv5361118translocation1nstd200human GRCh38 chr2: 148,900,784-148,900,784 , GRCh38 chr2: 148,900,865-148,900,865 , GRCh37.p13 chr2: 149,658,434-149,658,434 , GRCh37.p13 chr2: 149,658,353-149,658,353 LOC101928553, KIF5C
    nsv5177963mobile element insertion1nstd203human GRCh38 chr2: 148,957,970-148,957,985 , GRCh37.p13 chr2: 149,814,484-149,814,499 KIF5C
    nsv5172803mobile element insertion1nstd203human GRCh38 chr2: 149,026,206-149,026,221 , GRCh37.p13 chr2: 149,882,720-149,882,735 KIF5C
    nsv5063373mobile element insertion1nstd203human GRCh38 chr2: 148,979,164-148,979,180 , GRCh37.p13 chr2: 149,835,678-149,835,694 KIF5C
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
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