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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112754copy number variation1nstd102humanPathogenic GRCh37 chr4: 131,303,317-168,722,402 , GRCh38.p12 chr4: 130,382,162-167,801,251 MIR3139, CLGN, 407 more genes
    nsv5967014insertion1nstd209human GRCh38 chr4: 151,241,560-151,241,560 , GRCh37.p13 chr4: 152,162,712-152,162,712 SH3D19
    nsv5964111insertion1nstd209human GRCh38 chr4: 151,311,107-151,311,107 , GRCh37.p13 chr4: 152,232,259-152,232,259 SH3D19
    nsv5962838insertion1nstd209human GRCh38 chr4: 151,240,948-151,240,948 , GRCh37.p13 chr4: 152,162,100-152,162,100 SH3D19
    nsv5903040copy number variation1nstd209human GRCh38 chr4: 151,154,285-151,154,431 , GRCh37.p13 chr4: 152,075,437-152,075,583 SH3D19
    nsv5899498copy number variation1nstd209human GRCh38 chr4: 151,123,538-151,138,902 , GRCh37.p13 chr4: 152,044,690-152,060,054 SH3D19, LOC107986196
    nsv5899291copy number variation1nstd209human GRCh38 chr4: 151,153,199-151,153,282 , GRCh37.p13 chr4: 152,074,351-152,074,434 SH3D19
    nsv5893733copy number variation1nstd209human GRCh38 chr4: 151,240,192-151,241,979 , GRCh37.p13 chr4: 152,161,344-152,163,131 SH3D19
    nsv5890811copy number variation1nstd209human GRCh38 chr4: 151,280,054-151,280,109 , GRCh37.p13 chr4: 152,201,206-152,201,261 SH3D19, PRSS48
    nsv5890610copy number variation1nstd209human GRCh38 chr4: 151,161,878-151,164,699 , GRCh37.p13 chr4: 152,083,030-152,085,851 SH3D19
    nsv5890360copy number variation1nstd209human GRCh38 chr4: 151,316,096-151,317,298 , GRCh37.p13 chr4: 152,237,248-152,238,450 SH3D19
    nsv5888115copy number variation1nstd209human GRCh38 chr4: 151,308,068-151,309,030 , GRCh37.p13 chr4: 152,229,220-152,230,182 SH3D19
    nsv5838350copy number variation1nstd209human GRCh38 chr4: 151,307,981-151,309,098 , GRCh37.p13 chr4: 152,229,133-152,230,250 SH3D19
    nsv5838062copy number variation1nstd209human GRCh38 chr4: 151,162,216-151,164,690 , GRCh37.p13 chr4: 152,083,368-152,085,842 SH3D19
    nsv5838061copy number variation1nstd209human GRCh38 chr4: 151,123,495-151,130,846 , GRCh37.p13 chr4: 152,044,647-152,051,998 SH3D19, LOC107986196
    nsv5837751copy number variation1nstd209human GRCh38 chr4: 151,240,224-151,241,960 , GRCh37.p13 chr4: 152,161,376-152,163,112 SH3D19
    nsv5728045mobile element insertion1nstd211human GRCh38 chr4: 151,301,061-151,301,061 , GRCh37.p13 chr4: 152,222,213-152,222,213 RNU6-1282P, SH3D19
    nsv5717159mobile element insertion2nstd211human GRCh38 chr4: 151,234,565-151,234,565 , GRCh37.p13 chr4: 152,155,717-152,155,717 SH3D19
    nsv5715616mobile element insertion2nstd211human GRCh38 chr4: 151,302,552-151,302,552 , GRCh37.p13 chr4: 152,223,704-152,223,704 SH3D19
    nsv5622656insertion1nstd207human GRCh38 chr4: 151,214,795-151,214,795 , GRCh37.p13 chr4: 152,135,947-152,135,947 SH3D19
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