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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112742copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 164,696,665-164,751,252 , GRCh38.p12 chr3: 164,978,877-165,033,464 SI
    nsv6112731copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 164,714,302-164,716,481 , GRCh38.p12 chr3: 164,996,514-164,998,693 SI
    nsv5904530copy number variation1nstd209human GRCh38 chr3: 164,989,047-164,990,856 , GRCh37.p13 chr3: 164,706,835-164,708,644 SI
    nsv5834748copy number variation2nstd209human GRCh38 chr3: 165,008,224-165,009,423 , GRCh37.p13 chr3: 164,726,012-164,727,211 SI
    nsv5726038mobile element insertion1nstd211human GRCh38 chr3: 165,020,745-165,020,745 , GRCh37.p13 chr3: 164,738,533-164,738,533 SI
    nsv5683744mobile element insertion1nstd211human GRCh38 chr3: 165,061,645-165,061,645 , GRCh37.p13 chr3: 164,779,433-164,779,433 SI
    nsv5675967mobile element insertion2nstd211human GRCh38 chr3: 165,031,240-165,031,240 , GRCh37.p13 chr3: 164,749,028-164,749,028 SI
    nsv5673631copy number variation1nstd102humanUncertain significance GRCh37 chr3: 164,768,851-164,768,852 , GRCh38 chr3: 165,051,063-165,051,064 SI
    nsv5614290insertion1nstd207human GRCh38 chr3: 165,070,264-165,070,264 , GRCh37.p13 chr3: 164,788,052-164,788,052 LOC105374192, SI
    nsv5606138insertion1nstd207human GRCh38 chr3: 165,029,581-165,029,581 , GRCh37.p13 chr3: 164,747,369-164,747,369 SI
    nsv5551382insertion1nstd206human GRCh38 chr3: 165,029,622-165,029,632 , GRCh37.p13 chr3: 164,747,410-164,747,420 SI
    nsv5537970insertion1nstd206human GRCh38 chr3: 165,029,619-165,029,632 , GRCh37.p13 chr3: 164,747,407-164,747,420 SI
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5449342copy number variation1nstd206human GRCh38 chr3: 165,059,605-165,060,482 , GRCh37.p13 chr3: 164,777,393-164,778,270 SI
    nsv5437927copy number variation1nstd206human GRCh38 chr3: 165,050,402-165,050,460 , GRCh37.p13 chr3: 164,768,190-164,768,248 SI
    nsv5396729mobile element insertion1nstd206human GRCh38 chr3: 165,031,240-165,031,291 , GRCh37.p13 chr3: 164,749,028-164,749,079 SI
    nsv5367174translocation1nstd200human GRCh38 chr3: 165,059,952-165,059,952 , GRCh38 chr3: 165,059,289-165,059,289 , GRCh37.p13 chr3: 164,777,077-164,777,077 , GRCh37.p13 chr3: 164,777,740-164,777,740 SI
    nsv5352129translocation1nstd200human GRCh38 chr3: 165,030,040-165,030,040 , GRCh38 chr3: 165,031,189-165,031,189 , GRCh37.p13 chr3: 164,748,977-164,748,977 , GRCh37.p13 chr3: 164,747,828-164,747,828 SI
    nsv5340551translocation1nstd200human GRCh37 chr3: 164,777,077-164,777,077 , GRCh37 chr3: 164,777,740-164,777,740 , GRCh38.p12 chr3: 165,059,289-165,059,289 , GRCh38.p12 chr3: 165,059,952-165,059,952 SI
    nsv5312621copy number variation1nstd204human GRCh38.p13 chr3: 164,977,211-165,080,339 , GRCh37.p13 chr3: 164,694,999-164,798,127 SI, LOC105374192
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