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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096952copy number variation3nstd102humanUncertain significance GRCh37 chr3: 188,118,572-192,126,012 , GRCh38.p12 chr3: 188,400,784-192,408,223 P3H2, GMNC, 39 more genes
    nsv7096556copy number variation1nstd102humanUncertain significance GRCh37 chr3: 189,455,509-192,126,012 , GRCh38.p12 chr3: 189,737,720-192,408,223 LOC107986171, OSTN, 30 more genes
    nsv7053953inversion1nstd229human GRCh38 chr3: 190,927,904-191,666,058 , GRCh37.p13 chr3: 190,645,693-191,383,847 PYDC2, OSTN, 5 more genes
    nsv7040429inversion1nstd229human GRCh38 chr3: 184,379,670-192,292,047 , GRCh37.p13 chr3: 184,097,458-192,009,836 LOC107986163, RPL34P10, 123 more genes
    nsv6735893copy number variation1nstd229human GRCh38 chr3: 191,225,801-191,310,400 , GRCh37.p13 chr3: 190,943,590-191,028,189 UTS2B, OSTN-AS1, 1 more genes
    nsv6735765copy number variation1nstd229human GRCh38 chr3: 191,316,914-191,316,940 , GRCh37.p13 chr3: 191,034,703-191,034,729 UTS2B
    nsv6734923copy number variation1nstd229human GRCh38 chr3: 191,305,801-191,317,700 , GRCh37.p13 chr3: 191,023,590-191,035,489 UTS2B
    nsv6733684copy number variation1nstd229human GRCh38 chr3: 191,283,401-191,295,600 , GRCh37.p13 chr3: 191,001,190-191,013,389 UTS2B
    nsv6733518copy number variation1nstd229human GRCh38 chr3: 189,977,007-192,427,323 , GRCh37.p13 chr3: 189,694,796-192,145,112 RN7SKP296, LOC105374277, 27 more genes
    nsv6733372copy number variation1nstd229human GRCh38 chr3: 191,163,666-192,104,583 , GRCh37.p13 chr3: 190,881,455-191,822,372 LOC105374276, PYDC2-AS1, 10 more genes
    nsv6732616copy number variation1nstd229human GRCh38 chr3: 191,296,197-191,302,226 , GRCh37.p13 chr3: 191,013,986-191,020,015 UTS2B
    nsv6730769copy number variation1nstd229human GRCh38 chr3: 191,302,334-191,460,338 , GRCh37.p13 chr3: 191,020,123-191,178,127 UTS2B, PYDC2, 2 more genes
    nsv6730062copy number variation1nstd229human GRCh38 chr3: 191,222,801-191,616,500 , GRCh37.p13 chr3: 190,940,590-191,334,289 PYDC2, OSTN, 4 more genes
    nsv6729865copy number variation1nstd229human GRCh38 chr3: 191,324,317-191,354,319 , GRCh37.p13 chr3: 191,042,106-191,072,108 CCDC50, UTS2B
    nsv6729801copy number variation1nstd229human GRCh38 chr3: 191,294,001-191,299,800 , GRCh37.p13 chr3: 191,011,790-191,017,589 UTS2B
    nsv6728835copy number variation1nstd229human GRCh38 chr3: 191,262,423-191,306,289 , GRCh37.p13 chr3: 190,980,212-191,024,078 OSTN, UTS2B
    nsv6725513copy number variation1nstd229human GRCh38 chr3: 191,266,692-191,266,764 , GRCh37.p13 chr3: 190,984,481-190,984,553 UTS2B
    nsv6725168copy number variation1nstd229human GRCh38 chr3: 191,293,423-191,295,879 , GRCh37.p13 chr3: 191,011,212-191,013,668 UTS2B
    nsv6724252copy number variation1nstd229human GRCh38 chr3: 191,283,462-191,283,488 , GRCh37.p13 chr3: 191,001,251-191,001,277 UTS2B
    nsv6722744copy number variation1nstd229human GRCh38 chr3: 191,270,898-191,282,969 , GRCh37.p13 chr3: 190,988,687-191,000,758 UTS2B
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