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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5902579copy number variation1nstd209human GRCh38 chr5: 141,606,457-141,610,419 , GRCh37.p13 chr5: 140,986,024-140,989,986 DIAPH1
    nsv5896786copy number variation1nstd209human GRCh38 chr5: 141,594,141-141,594,543 , GRCh37.p13 chr5: 140,973,708-140,974,110 DIAPH1
    nsv5888880copy number variation1nstd209human GRCh38 chr5: 141,531,914-141,531,973 , GRCh37.p13 chr5: 140,911,481-140,911,540 DIAPH1
    nsv5841455copy number variation1nstd209human GRCh38 chr5: 141,606,336-141,610,454 , GRCh37.p13 chr5: 140,985,903-140,990,021 DIAPH1
    nsv5693268mobile element insertion1nstd211human GRCh38 chr5: 141,534,421-141,534,421 , GRCh37.p13 chr5: 140,913,988-140,913,988 DIAPH1
    nsv5461815copy number variation1nstd206human GRCh38 chr5: 141,594,504-141,595,042 , GRCh37.p13 chr5: 140,974,071-140,974,609 DIAPH1
    nsv5461380copy number variation1nstd206human GRCh38 chr5: 141,603,976-141,604,396 , GRCh37.p13 chr5: 140,983,543-140,983,963 DIAPH1
    nsv5458817copy number variation1nstd206human GRCh38 chr5: 141,588,534-141,588,617 , GRCh37.p13 chr5: 140,968,101-140,968,184 RPS27AP10, DIAPH1
    nsv5457867copy number variation1nstd206human GRCh38 chr5: 141,581,567-141,581,695 , GRCh37.p13 chr5: 140,961,134-140,961,262 DIAPH1
    nsv5407744mobile element insertion1nstd206human GRCh38 chr5: 141,581,383-141,581,434 , GRCh37.p13 chr5: 140,960,950-140,961,001 DIAPH1
    nsv5381814inversion1nstd102humanLikely pathogenic GRCh37 chr5: 140,903,674-140,903,846 , GRCh38 chr5: 141,524,107-141,524,279 DIAPH1
    nsv5381510copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,633,338-140,998,481 , GRCh38.p12 chr5: 137,297,649-141,618,914 RNA5SP195, LOC112267855, 174 more genes
    nsv5378124translocation1nstd200human GRCh38 chr5: 141,570,789-141,570,789 , GRCh38 chr5: 141,568,986-141,568,986 , GRCh37.p13 chr5: 140,950,356-140,950,356 , GRCh37.p13 chr5: 140,948,553-140,948,553 DIAPH1
    nsv5326844translocation1nstd204human GRCh38.p13 chr5: 141,605,259-141,605,259 , GRCh38.p13 chr5: 141,605,988-141,605,988 , GRCh37.p13 chr5: 140,984,826-140,984,826 , GRCh37.p13 chr5: 140,985,555-140,985,555 DIAPH1
    nsv5094147mobile element insertion1nstd203human GRCh38 chr5: 141,539,276-141,539,294 , GRCh37.p13 chr5: 140,918,843-140,918,861 DIAPH1
    nsv5085153mobile element insertion1nstd203human GRCh38 chr5: 141,608,836-141,608,852 , GRCh37.p13 chr5: 140,988,403-140,988,419 DIAPH1
    nsv5080943mobile element insertion1nstd203human GRCh38 chr5: 141,602,388-141,602,392 , GRCh37.p13 chr5: 140,981,955-140,981,959 DIAPH1
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4945165copy number variation1nstd200human GRCh38 chr5: 141,541,412-141,545,411 , GRCh37.p13 chr5: 140,920,979-140,924,978 DIAPH1
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