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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
    nsv6736074copy number variation1nstd229human GRCh38 chr3: 191,394,513-191,394,807 , GRCh37.p13 chr3: 191,112,302-191,112,596 CCDC50
    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
    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
    nsv6730510copy number variation1nstd229human GRCh38 chr3: 191,361,160-191,369,916 , GRCh37.p13 chr3: 191,078,949-191,087,705 CCDC50
    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
    nsv6729957copy number variation1nstd229human GRCh38 chr3: 191,334,453-191,334,499 , GRCh37.p13 chr3: 191,052,242-191,052,288 CCDC50
    nsv6729865copy number variation1nstd229human GRCh38 chr3: 191,324,317-191,354,319 , GRCh37.p13 chr3: 191,042,106-191,072,108 CCDC50, UTS2B
    nsv6722421copy number variation1nstd229human GRCh38 chr3: 191,346,896-191,353,871 , GRCh37.p13 chr3: 191,064,685-191,071,660 CCDC50
    nsv6634371copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 171,549,421-198,022,430 , GRCh38.p12 chr3: 171,831,631-198,235,559 ACTL6A, AHSG, 466 more genes
    nsv6628499copy number variation1nstd224human GRCh37 chr3: 191,043,229-191,100,568 , GRCh38.p12 chr3: 191,325,440-191,382,779 CCDC50, UTS2B
    nsv6367267copy number variation1nstd223human GRCh38 chr3: 189,977,006-192,427,321 , GRCh37.p13 chr3: 189,694,795-192,145,110 RN7SKP296, LOC100129725, 27 more genes
    nsv6315437copy number variation1nstd102humanPathogenic GRCh37 chr3: 183,498,520-197,851,986 , GRCh38.p12 chr3: 183,780,732-198,125,115 LOC105374291, GP5, 315 more genes
    nsv6311973copy number variation1nstd102humanUncertain significance GRCh37 chr3: 191,074,857-191,109,549 , GRCh38.p12 chr3: 191,357,068-191,391,760 CCDC50
    nsv6298364copy number variation1nstd186human GRCh37 chr3: 190,724,093-191,269,493 , GRCh38.p12 chr3: 191,006,304-191,551,704 CCDC50, PYDC2, 5 more genes
    nsv6291041copy number variation1nstd102humanUncertain significance GRCh37 chr3: 190,414,517-191,108,120 , GRCh38.p12 chr3: 190,696,728-191,390,331 GMNC, CCT6P4, 8 more genes
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