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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5962669insertion1nstd209human GRCh38 chr3: 49,367,342-49,367,342 , GRCh37.p13 chr3: 49,404,775-49,404,775 RHOA
    nsv5952574insertion1nstd209human GRCh38 chr3: 49,399,054-49,399,054 , GRCh37.p13 chr3: 49,436,487-49,436,487 RHOA
    nsv5948684insertion1nstd209human GRCh38 chr3: 49,404,094-49,404,094 , GRCh37.p13 chr3: 49,441,527-49,441,527 RHOA
    nsv5890519copy number variation1nstd209human GRCh38 chr3: 49,395,059-49,400,841 , GRCh37.p13 chr3: 49,432,492-49,438,274 RHOA
    nsv5887908copy number variation1nstd209human GRCh38 chr3: 49,376,857-49,377,320 , GRCh37.p13 chr3: 49,414,290-49,414,753 RHOA
    nsv5836319copy number variation1nstd209human GRCh38 chr3: 49,395,081-49,398,480 , GRCh37.p13 chr3: 49,432,514-49,435,913 RHOA
    nsv5836058copy number variation1nstd209human GRCh38 chr3: 49,408,413-49,410,021 , GRCh37.p13 chr3: 49,445,846-49,447,454 RHOA
    nsv5729826mobile element insertion2nstd211human GRCh38 chr3: 49,384,526-49,384,526 , GRCh37.p13 chr3: 49,421,959-49,421,959 RHOA
    nsv5729583mobile element insertion1nstd211human GRCh38 chr3: 49,373,873-49,373,873 , GRCh37.p13 chr3: 49,411,306-49,411,306 RHOA
    nsv5714629mobile element insertion1nstd211human GRCh38 chr3: 49,404,095-49,404,095 , GRCh37.p13 chr3: 49,441,528-49,441,528 RHOA
    nsv5673729copy number variation1nstd102humanPathogenic GRCh37 chr3: 48,507,870-50,340,407 , GRCh38.p12 chr3: 48,466,471-50,302,976 SEMA3B-AS1, GNAT1, 87 more genes
    nsv5605727insertion1nstd207human GRCh38 chr3: 49,404,094-49,404,094 , GRCh37.p13 chr3: 49,441,527-49,441,527 RHOA
    nsv5563023sequence alteration1nstd206human GRCh38 chr3: 49,404,422-49,405,234 , GRCh37.p13 chr3: 49,441,855-49,442,667 RHOA
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5561650mobile element insertion1nstd206human GRCh38 chr3: 49,373,885-49,373,924 , GRCh37.p13 chr3: 49,411,318-49,411,357 RHOA
    nsv5535033insertion1nstd206human GRCh38 chr3: 49,404,094-49,404,094 , GRCh37.p13 chr3: 49,441,527-49,441,527 RHOA
    nsv5447503copy number variation1nstd206human GRCh38 chr3: 49,368,985-49,369,309 , GRCh37.p13 chr3: 49,406,418-49,406,742 RHOA
    nsv5443438copy number variation1nstd206human GRCh38 chr3: 49,390,892-49,395,587 , GRCh37.p13 chr3: 49,428,325-49,433,020 RHOA
    nsv5442746copy number variation1nstd206human GRCh38 chr3: 49,387,186-49,389,729 , GRCh37.p13 chr3: 49,424,619-49,427,162 RHOA
    nsv5440205copy number variation1nstd206human GRCh38 chr3: 49,394,982-49,400,969 , GRCh37.p13 chr3: 49,432,415-49,438,402 RHOA
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