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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6628460copy number variation1nstd224human GRCh37 chr3: 151,161,112-151,342,245 , GRCh38.p12 chr3: 151,443,324-151,624,457 IGSF10, MIR5186, 2 more genes
    nsv6355771copy number variation1nstd223human GRCh38 chr3: 151,564,859-151,565,505 , GRCh37.p13 chr3: 151,282,647-151,283,293 MIR5186, IGSF10
    nsv6313678copy number variation1nstd102humanPathogenic GRCh37 chr3: 145,486,960-160,504,834 , GRCh38.p12 chr3: 145,769,173-160,787,046 RNU6-901P, RPL32P8, 229 more genes
    nsv6313632copy number variation1nstd102humanUncertain significance GRCh37 chr3: 151,147,204-154,845,718 , GRCh38.p12 chr3: 151,429,416-155,127,929 LOC105374171, ARHGEF26-AS1, 42 more genes
    nsv6290273copy number variation1nstd102humanPathogenic GRCh37 chr3: 142,729,607-157,921,084 , GRCh38.p12 chr3: 143,010,765-158,203,295 LINC02066, TM4SF1-AS1, 206 more genes
    nsv6290244copy number variation1nstd102humanPathogenic GRCh37 chr3: 143,439,359-165,252,122 , GRCh38.p12 chr3: 143,720,517-165,534,334 LOC102724145, C3orf80, 273 more genes
    nsv6134674copy number variation1nstd213human GRCh37 chr3: 150,600,000-153,170,001 , GRCh38.p12 chr3: 150,882,213-153,452,212 CLRN1-AS1, MBNL1-AS1, 37 more genes
    nsv5889564copy number variation1nstd209human GRCh38 chr3: 151,537,872-151,581,156 , GRCh37.p13 chr3: 151,255,660-151,298,944 MIR5186, IGSF10
    nsv5381765copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,173,683-162,494,699 , GRCh38.p12 chr3: 138,454,841-162,776,911 MBNL1-AS1, LOC107986138, 339 more genes
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
    nsv4912390copy number variation1nstd200human GRCh38 chr3: 151,409,405-152,510,511 , GRCh37.p13 chr3: 151,127,193-152,228,300 , IGSF10, 17 more genes
    nsv4684209copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,145,289-162,275,610 , GRCh38.p12 chr3: 138,426,447-162,557,822 MTAPP1, PLS1, 339 more genes
    nsv4678885copy number variation1nstd189human GRCh37.p13 chr3: 151,212,763-151,483,819 , GRCh38.p12 chr3: 151,494,975-151,766,031 , GRCh38.p12 chr3|NW_003315913.1: 1-180,671 IGSF10, AADACL2, 4 more genes
    nsv4674301copy number variation1nstd102humanPathogenic GRCh37 chr3: 149,404,255-152,786,331 , GRCh38.p12 chr3: 149,686,468-153,068,542 EIF3JP2, IGSF10, 63 more genes
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv4327115inversion1nstd166human GRCh37.p13 chr3: 131,882,701-162,233,318 , GRCh38.p12 chr3: 132,163,857-162,515,530 , ATP1B3, 446 more genes
    nsv4106707copy number variation1nstd166human GRCh37.p13 chr3: 151,253,151-151,293,697 , GRCh38.p12 chr3: 151,535,363-151,575,909 MIR5186, IGSF10
    nsv4092850copy number variation1nstd166human GRCh37.p13 chr3: 151,282,601-151,283,649 , GRCh38.p12 chr3: 151,564,813-151,565,861 IGSF10, MIR5186
    nsv3957518insertion1nstd168human GRCh38 chr3: 151,545,347-151,578,528 , GRCh37.p13 chr3: 151,263,135-151,296,316 IGSF10, MIR5186
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