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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5906645copy number variation1nstd209human GRCh38 chr4: 73,158,131-73,158,190 , GRCh37.p13 chr4: 74,023,848-74,023,907 ANKRD17
    nsv5906036copy number variation1nstd209human GRCh38 chr4: 73,191,329-73,191,400 , GRCh37.p13 chr4: 74,057,046-74,057,117 ANKRD17
    nsv5903519copy number variation1nstd209human GRCh38 chr4: 73,160,521-73,160,620 , GRCh37.p13 chr4: 74,026,238-74,026,337 ANKRD17
    nsv5893576copy number variation1nstd209human GRCh38 chr4: 67,920,462-75,134,545 , GRCh37.p13 chr4: 68,786,180-76,059,755 , DCK, 147 more genes
    nsv5888243copy number variation1nstd209human GRCh38 chr4: 73,205,673-73,205,802 , GRCh37.p13 chr4: 74,071,390-74,071,519 ANKRD17
    nsv5683338mobile element insertion1nstd211human GRCh38 chr4: 73,108,416-73,108,416 , GRCh37.p13 chr4: 73,974,133-73,974,133 ANKRD17
    nsv5683232mobile element insertion1nstd211human GRCh38 chr4: 73,178,491-73,178,491 , GRCh37.p13 chr4: 74,044,208-74,044,208 ANKRD17
    nsv5682079mobile element insertion1nstd211human GRCh38 chr4: 73,164,305-73,164,305 , GRCh37.p13 chr4: 74,030,022-74,030,022 ANKRD17
    nsv5681989mobile element insertion1nstd211human GRCh38 chr4: 73,130,279-73,130,279 , GRCh37.p13 chr4: 73,995,996-73,995,996 ANKRD17
    nsv5674237copy number variation1nstd102humanPathogenic GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872 FTLP10, RNU6-410P, 335 more genes
    nsv5559652mobile element insertion1nstd206human GRCh38 chr4: 73,243,097-73,243,097 , GRCh37.p13 chr4: 74,108,814-74,108,814 ANKRD17
    nsv5547577insertion1nstd206human GRCh38 chr4: 73,211,082-73,211,133 , GRCh37.p13 chr4: 74,076,799-74,076,850 ANKRD17
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5469826copy number variation1nstd206human GRCh38 chr4: 73,106,788-73,108,465 , GRCh37.p13 chr4: 73,972,505-73,974,182 ANKRD17
    nsv5468457copy number variation1nstd206human GRCh38 chr4: 73,129,801-73,132,611 , GRCh37.p13 chr4: 73,995,518-73,998,328 ANKRD17
    nsv5467245copy number variation1nstd206human GRCh38 chr4: 73,203,525-73,205,401 , GRCh37.p13 chr4: 74,069,242-74,071,118 ANKRD17
    nsv5455715copy number variation1nstd206human GRCh38 chr4: 73,193,887-73,194,056 , GRCh37.p13 chr4: 74,059,604-74,059,773 ANKRD17
    nsv5411781mobile element insertion1nstd206human GRCh38 chr4: 73,164,305-73,164,310 , GRCh37.p13 chr4: 74,030,022-74,030,027 ANKRD17
    nsv5401063mobile element insertion1nstd206human GRCh38 chr4: 73,130,279-73,130,330 , GRCh37.p13 chr4: 73,995,996-73,996,047 ANKRD17
    nsv5313097copy number variation1nstd204human GRCh38.p13 chr4: 73,129,776-73,132,633 , GRCh37.p13 chr4: 73,995,493-73,998,350 ANKRD17
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