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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7044513inversion1nstd229human GRCh38 chr3: 131,210,998-138,882,695 , GRCh37.p13 chr3: 130,929,842-138,601,537 HSPA8P9, RNU6-1174P, 114 more genes
    nsv6733759copy number variation1nstd229human GRCh38 chr3: 131,527,054-131,527,099 , GRCh37.p13 chr3: 131,245,898-131,245,943 BCL2L12P1
    nsv6731705copy number variation1nstd229human GRCh38 chr3: 131,384,002-132,144,415 , GRCh37.p13 chr3: 131,102,846-131,863,259 SNORA58, NUDT16, 9 more genes
    nsv6719114copy number variation1nstd229human GRCh38 chr3: 131,519,333-131,527,300 , GRCh37.p13 chr3: 131,238,177-131,246,144 BCL2L12P1, LOC105374114
    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
    nsv6628642copy number variation1nstd224human GRCh37 chr3: 131,041,928-131,471,873 , GRCh38.p12 chr3: 131,323,084-131,753,029 NUDT16-DT, MRPL3, 9 more genes
    nsv6369922copy number variation1nstd223human GRCh38 chr3: 131,384,002-132,144,415 , GRCh37.p13 chr3: 131,102,846-131,863,259 LOC105374114, LOC105374111, 9 more genes
    nsv6311770copy number variation1nstd102humanPathogenic GRCh37 chr3: 120,365,818-133,465,047 , GRCh38.p12 chr3: 120,646,971-133,746,203 HNRNPA1P23, MIX23, 278 more genes
    nsv6134665copy number variation1nstd213human GRCh37 chr3: 131,150,000-131,700,001 , GRCh38.p12 chr3: 131,431,156-131,981,157 MRPL3, CPNE4, 5 more genes
    nsv6134575copy number variation1nstd213human GRCh37 chr3: 116,870,000-132,100,001 , GRCh38.p12 chr3: 117,151,153-132,381,157 ACP3, ADCY5, 308 more genes
    nsv6134491copy number variation1nstd213human GRCh37 chr3: 130,600,000-131,700,001 , GRCh38.p12 chr3: 130,881,156-131,981,157 MRPL3, ATP2C1, 16 more genes
    nsv6134401copy number variation1nstd213human GRCh37 chr3: 130,680,000-131,440,001 , GRCh38.p12 chr3: 130,961,156-131,721,157 MRPL3, ATP2C1, 12 more genes
    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
    nsv5896498copy number variation1nstd209human GRCh38 chr3: 131,512,293-131,532,540 , GRCh37.p13 chr3: 131,231,137-131,251,384 CPNE4, BCL2L12P1, 1 more genes
    nsv5834907copy number variation1nstd209human GRCh38 chr3: 131,512,195-131,532,344 , GRCh37.p13 chr3: 131,231,039-131,251,188 CPNE4, BCL2L12P1, 1 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
    nsv4777889mobile element deletion1nstd200human GRCh37 chr3: 131,244,548-131,244,855 , GRCh38.p12 chr3: 131,525,704-131,526,011 BCL2L12P1
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
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