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Items: 1 to 20 of 169

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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
    nsv6737129copy number variation1nstd229human GRCh38 chr3: 191,166,909-191,213,484 , GRCh37.p13 chr3: 190,884,698-190,931,273 OSTN-AS1, OSTN, 1 more genes
    nsv6736441copy number variation1nstd229human GRCh38 chr3: 191,104,868-191,182,103 , GRCh37.p13 chr3: 190,822,657-190,899,892 LOC107986171
    nsv6736070copy number variation1nstd229human GRCh38 chr3: 191,147,465-191,180,292 , GRCh37.p13 chr3: 190,865,254-190,898,081 LOC107986171
    nsv6734762copy number variation1nstd229human GRCh38 chr3: 191,167,124-191,170,671 , GRCh37.p13 chr3: 190,884,913-190,888,460 LOC107986171
    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
    nsv6732193copy number variation1nstd229human GRCh38 chr3: 190,618,702-191,189,943 , GRCh37.p13 chr3: 190,336,491-190,907,732 IL1RAP, GMNC, 7 more genes
    nsv6731980copy number variation1nstd229human GRCh38 chr3: 191,167,981-191,168,187 , GRCh37.p13 chr3: 190,885,770-190,885,976 LOC107986171
    nsv6729770copy number variation1nstd229human GRCh38 chr3: 191,156,177-191,188,967 , GRCh37.p13 chr3: 190,873,966-190,906,756 LOC107986171
    nsv6726687copy number variation1nstd229human GRCh38 chr3: 191,132,830-191,180,857 , GRCh37.p13 chr3: 190,850,619-190,898,646 LOC107986171
    nsv6724394copy number variation1nstd229human GRCh38 chr3: 191,135,601-191,159,200 , GRCh37.p13 chr3: 190,853,390-190,876,989 LOC107986171
    nsv6720928copy number variation1nstd229human GRCh38 chr3: 191,157,483-191,280,085 , GRCh37.p13 chr3: 190,875,272-190,997,874 UTS2B, LOC107986171, 2 more genes
    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
    nsv6628550copy number variation1nstd224human GRCh37 chr3: 190,873,984-190,891,939 , GRCh38.p12 chr3: 191,156,195-191,174,150 LOC107986171
    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
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