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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
    nsv5900256copy number variation1nstd209human GRCh38 chr4: 147,573,835-147,580,311 , GRCh37.p13 chr4: 148,494,987-148,501,463 LINC02507
    nsv5838293copy number variation1nstd209human GRCh38 chr4: 147,573,854-147,580,378 , GRCh37.p13 chr4: 148,495,006-148,501,530 LINC02507
    nsv5683865mobile element insertion1nstd211human GRCh38 chr4: 147,593,903-147,593,903 , GRCh37.p13 chr4: 148,515,055-148,515,055 LINC02507
    nsv5683662mobile element insertion2nstd211human GRCh38 chr4: 147,591,029-147,591,029 , GRCh37.p13 chr4: 148,512,181-148,512,181 LINC02507
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5473356copy number variation1nstd206human GRCh38 chr4: 147,573,885-147,580,303 , GRCh37.p13 chr4: 148,495,037-148,501,455 LINC02507
    nsv5457407copy number variation1nstd206human GRCh38 chr4: 147,595,244-147,614,726 , GRCh37.p13 chr4: 148,516,395-148,535,877 LINC02507
    nsv5399504mobile element insertion1nstd206human GRCh38 chr4: 147,591,029-147,591,080 , GRCh37.p13 chr4: 148,512,181-148,512,232 LINC02507
    nsv5394064mobile element insertion1nstd206human GRCh38 chr4: 147,593,903-147,593,954 , GRCh37.p13 chr4: 148,515,055-148,515,106 LINC02507
    nsv5309089copy number variation1nstd204human GRCh38.p13 chr4: 147,573,878-147,580,274 , GRCh37.p13 chr4: 148,495,030-148,501,426 LINC02507
    nsv5227466copy number variation1nstd204human GRCh38.p13 chr4: 147,573,031-147,580,266 , GRCh37.p13 chr4: 148,494,183-148,501,418 LINC02507
    nsv5226953copy number variation1nstd204human GRCh38.p13 chr4: 147,573,201-147,580,300 , GRCh37.p13 chr4: 148,494,353-148,501,452 LINC02507
    nsv5092870mobile element insertion1nstd203human GRCh38 chr4: 147,591,019-147,591,029 , GRCh37.p13 chr4: 148,512,171-148,512,181 LINC02507
    nsv5081049mobile element insertion1nstd203human GRCh38 chr4: 147,591,024-147,591,024 , GRCh37.p13 chr4: 148,512,176-148,512,176 LINC02507
    nsv4948546copy number variation1nstd200human GRCh38 chr4: 147,538,037-147,970,463 , GRCh37.p13 chr4: 148,459,189-148,891,614 , RNA5SP165, 8 more genes
    nsv4929525copy number variation1nstd200human GRCh38 chr4: 147,595,244-147,614,726 , GRCh37.p13 chr4: 148,516,395-148,535,877 LINC02507
    nsv4929524copy number variation1nstd200human GRCh38 chr4: 147,573,884-147,580,262 , GRCh37.p13 chr4: 148,495,036-148,501,414 LINC02507
    nsv4801067copy number variation1nstd200human GRCh37 chr4: 148,516,394-148,535,878 , GRCh38.p12 chr4: 147,595,243-147,614,727 LINC02507
    nsv4801066copy number variation1nstd200human GRCh37 chr4: 148,495,036-148,501,420 , GRCh38.p12 chr4: 147,573,884-147,580,268 LINC02507
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