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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131461insertion1nstd186human GRCh37 chr14: 64,087,618-64,087,618 , GRCh38.p12 chr14: 63,620,900-63,620,900 WDR89
    nsv5980451copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 54,654,001-75,828,024 , GRCh38.p12 chr14: 54,187,283-75,361,321 ACTN1, ACYP1, 400 more genes
    nsv5970602insertion1nstd209human GRCh38 chr14: 63,620,897-63,620,897 , GRCh37.p13 chr14: 64,087,615-64,087,615 WDR89
    nsv5940421copy number variation1nstd209human GRCh38 chr14: 63,624,281-63,625,973 , GRCh37.p13 chr14: 64,090,999-64,092,691 WDR89
    nsv5936277copy number variation1nstd209human GRCh38 chr14: 63,602,353-63,602,653 , GRCh37.p13 chr14: 64,069,071-64,069,371 WDR89, HSPE1P2
    nsv5928827copy number variation1nstd209human GRCh38 chr14: 63,624,540-63,624,639 , GRCh37.p13 chr14: 64,091,258-64,091,357 WDR89
    nsv5850579copy number variation1nstd209human GRCh38 chr14: 63,624,442-63,626,241 , GRCh37.p13 chr14: 64,091,160-64,092,959 WDR89
    nsv5723976mobile element insertion1nstd211human GRCh38 chr14: 63,633,604-63,633,604 , GRCh37.p13 chr14: 64,100,322-64,100,322 WDR89
    nsv5698166mobile element insertion1nstd211human GRCh38 chr14: 63,598,382-63,598,382 , GRCh37.p13 chr14: 64,065,100-64,065,100 WDR89
    nsv5651130insertion1nstd207human GRCh38 chr14: 63,620,897-63,620,897 , GRCh37.p13 chr14: 64,087,615-64,087,615 WDR89
    nsv5564009sequence alteration1nstd206human GRCh38 chr14: 63,471,626-63,659,036 , GRCh37.p13 chr14: 63,938,344-64,125,754 PPP2R5E, WDR89, 7 more genes
    nsv5560163mobile element insertion1nstd206human GRCh38 chr14: 63,633,604-63,633,655 , GRCh37.p13 chr14: 64,100,322-64,100,373 WDR89
    nsv5539946insertion1nstd206human GRCh38 chr14: 63,620,900-63,620,900 , GRCh37.p13 chr14: 64,087,618-64,087,618 WDR89
    nsv5507046copy number variation1nstd206human GRCh38 chr14: 63,471,637-63,635,175 , GRCh37.p13 chr14: 63,938,355-64,101,893 PPP2R5E, WDR89, 6 more genes
    nsv5498751copy number variation1nstd206human GRCh38 chr14: 63,610,932-63,612,018 , GRCh37.p13 chr14: 64,077,650-64,078,736 WDR89
    nsv5495499copy number variation1nstd206human GRCh38 chr14: 63,589,727-63,596,394 , GRCh37.p13 chr14: 64,056,445-64,063,112 GCATP1, WDR89
    nsv5419562mobile element insertion1nstd206human GRCh38 chr14: 63,598,382-63,598,433 , GRCh37.p13 chr14: 64,065,100-64,065,151 WDR89
    nsv5374579translocation1nstd200human GRCh38 chr14: 63,634,387-63,634,387 , GRCh38 chr14: 63,659,008-63,659,008 , GRCh37.p13 chr14: 64,101,105-64,101,105 , GRCh37.p13 chr14: 64,125,726-64,125,726 WDR89, LOC105370532
    nsv5333383translocation1nstd200human GRCh37 chr14: 64,125,681-64,125,681 , GRCh37 chr14: 64,101,105-64,101,105 , GRCh38.p12 chr14: 63,634,387-63,634,387 , GRCh38.p12 chr14: 63,658,963-63,658,963 WDR89, LOC105370532
    nsv5269977copy number variation1nstd204human GRCh38.p13 chr14: 63,590,598-63,596,072 , GRCh37.p13 chr14: 64,057,316-64,062,790 WDR89, GCATP1
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