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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112714copy number variation1nstd102humanPathogenic GRCh37 chr3: 127,927,712-136,889,323 , GRCh38.p12 chr3: 128,208,869-137,170,481 RNU6-789P, FAM86HP, 169 more genes
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv4914769copy number variation1nstd200human GRCh38 chr3: 131,384,001-132,144,416 , GRCh37.p13 chr3: 131,102,845-131,863,260 MRPL3, LOC107986025, 9 more genes
    nsv4794339copy number variation1nstd200human GRCh37 chr3: 131,102,845-131,863,260 , GRCh38.p12 chr3: 131,384,001-132,144,416 MRPL3, LOC105374111, 9 more genes
    nsv4685634copy number variation1nstd102humanUncertain significance GRCh37 chr3: 131,507,971-132,143,591 , GRCh38.p12 chr3: 131,789,127-132,424,747 LOC105374111, ACP3, 10 more genes
    nsv4674665copy number variation1nstd102humanLikely benign GRCh37 chr3: 131,649,934-131,884,654 , GRCh38.p12 chr3: 131,931,090-132,165,810 CPNE4, LOC105374111, 1 more genes
    nsv4394129copy number variation1nstd174human GRCh37 chr3: 131,696,103-131,713,566 , GRCh38.p12 chr3: 131,977,259-131,994,722 CPNE4, MIR5704
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv3970886copy number variation1nstd168human GRCh38 chr3: 131,939,502-132,009,573 , GRCh37.p13 chr3: 131,658,346-131,728,417 CPNE4, MIR5704
    nsv3957292insertion1nstd168human GRCh38 chr3: 131,965,665-131,985,551 , GRCh37.p13 chr3: 131,684,509-131,704,395 CPNE4, MIR5704
    nsv3922717copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,002,154-146,895,858 , GRCh38 chr3: 93,800,620-145,695,381 , GRCh37 chr3: 93,519,464-145,413,168 OR7E53P, HSPA8P9, 794 more genes
    nsv3920834copy number variation1nstd102humanUncertain significance NCBI36 chr3: 127,308,312-142,119,621 , GRCh38 chr3: 126,106,779-140,918,089 , GRCh37 chr3: 125,825,622-140,636,931 NCK1-DT, LOC107986126, 271 more genes
    nsv3920279copy number variation1nstd102humanPathogenic GRCh38 chr3: 129,817,243-143,381,624 , GRCh37 chr3: 129,536,086-143,100,466 , NCBI36 chr3: 131,018,776-144,583,156 NPHP3-AS1, RNA5SP142, 218 more genes
    nsv3918981copy number variation1nstd102humanPathogenic GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446 LINC02614, LINC02054, 1469 more genes
    nsv3918871copy number variation1nstd102humanPathogenic GRCh38 chr3: 130,401,265-139,005,019 , NCBI36 chr3: 131,602,799-140,206,551 , GRCh37 chr3: 130,120,109-138,723,861 FOXL2, NPHP3, 132 more genes
    nsv3914757copy number variation1nstd102humanPathogenic NCBI36 chr3: 131,018,776-142,626,687 , GRCh38 chr3: 129,817,243-141,425,155 , GRCh37 chr3: 129,536,086-141,143,997 CLSTN2-AS1, COPB2, 177 more genes
    nsv3912335copy number variation1nstd102humanLikely pathogenic NCBI36 chr3: 128,809,478-134,768,195 , GRCh37 chr3: 127,326,788-133,285,505 , GRCh38 chr3: 127,607,945-133,566,661 ACP3, FTH1P4, 130 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 NDUFB4, LOC105374108, 2876 more genes
    nsv3886396copy number variation1nstd102humanBenign GRCh37 chr3: 131,696,103-131,713,566 , GRCh38.p12 chr3: 131,977,259-131,994,722 MIR5704, CPNE4
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 RNU4-62P, SEMA3B-AS1, 2880 more genes
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