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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5952105insertion1nstd209human GRCh38 chr4: 174,926,872-174,926,872 , GRCh37.p13 chr4: 175,848,023-175,848,023 ADAM29
    nsv5895144copy number variation1nstd209human GRCh38 chr4: 174,977,727-174,977,780 , GRCh37.p13 chr4: 175,898,878-175,898,931 ADAM29
    nsv5888746copy number variation1nstd209human GRCh38 chr4: 174,963,953-174,965,831 , GRCh37.p13 chr4: 175,885,104-175,886,982 ADAM29
    nsv5838441copy number variation2nstd209human GRCh38 chr4: 174,963,909-174,965,901 , GRCh37.p13 chr4: 175,885,060-175,887,052 ADAM29
    nsv5639208insertion1nstd207human GRCh38 chr4: 174,977,850-174,977,850 , GRCh37.p13 chr4: 175,899,001-175,899,001 ADAM29
    nsv5566872copy number variation1nstd207human GRCh38 chr4: 174,977,937-174,977,990 , GRCh37.p13 chr4: 175,899,088-175,899,141 ADAM29
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5549840insertion1nstd206human GRCh38 chr4: 174,926,871-174,926,874 , GRCh37.p13 chr4: 175,848,022-175,848,025 ADAM29
    nsv5462641copy number variation1nstd206human GRCh38 chr4: 174,843,833-175,491,000 , GRCh37.p13 chr4: 175,764,984-176,412,151 LOC105377552, LOC100129957, 3 more genes
    nsv5459630copy number variation1nstd206human GRCh38 chr4: 174,943,748-174,943,817 , GRCh37.p13 chr4: 175,864,899-175,864,968 ADAM29
    nsv5458353copy number variation1nstd206human GRCh38 chr4: 174,963,958-174,965,832 , GRCh37.p13 chr4: 175,885,109-175,886,983 ADAM29
    nsv5361983translocation1nstd200human GRCh38 chr4: 174,965,832-174,965,832 , GRCh38 chr4: 174,963,958-174,963,958 , GRCh37.p13 chr4: 175,885,109-175,885,109 , GRCh37.p13 chr4: 175,886,983-175,886,983 ADAM29
    nsv5329598translocation1nstd200human GRCh37 chr4: 175,886,983-175,886,983 , GRCh37 chr4: 175,885,109-175,885,109 , GRCh38.p12 chr4: 174,965,832-174,965,832 , GRCh38.p12 chr4: 174,963,958-174,963,958 ADAM29
    nsv5240309copy number variation1nstd204human GRCh38.p13 chr4: 174,953,901-174,959,300 , GRCh37.p13 chr4: 175,875,052-175,880,451 ADAM29
    nsv4944062copy number variation1nstd200human GRCh38 chr4: 173,724,041-174,933,391 , GRCh37.p13 chr4: 174,645,192-175,854,542 LOC107986204, LOC101928551, 16 more genes
    nsv4930069copy number variation1nstd200human GRCh38 chr4: 174,950,679-174,951,815 , GRCh37.p13 chr4: 175,871,830-175,872,966 ADAM29
    nsv4930068copy number variation1nstd200human GRCh38 chr4: 174,945,744-174,952,114 , GRCh37.p13 chr4: 175,866,895-175,873,265 ADAM29
    nsv4930067copy number variation1nstd200human GRCh38 chr4: 174,915,174-174,925,627 , GRCh37.p13 chr4: 175,836,325-175,846,778 ADAM29
    nsv4801796copy number variation1nstd200human GRCh37 chr4: 175,866,895-175,873,265 , GRCh38.p12 chr4: 174,945,744-174,952,114 ADAM29
    nsv4794687copy number variation1nstd200human GRCh37 chr4: 174,645,192-175,854,542 , GRCh38.p12 chr4: 173,724,041-174,933,391 LOC105377547, LINC02269, 16 more genes
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