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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
    nsv7040429inversion1nstd229human GRCh38 chr3: 184,379,670-192,292,047 , GRCh37.p13 chr3: 184,097,458-192,009,836 LOC107986163, RPL34P10, 123 more genes
    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
    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
    nsv6729305copy number variation1nstd229human GRCh38 chr3: 190,831,001-190,854,300 , GRCh37.p13 chr3: 190,548,790-190,572,089 ENAHP1, GMNC
    nsv6727722copy number variation1nstd229human GRCh38 chr3: 190,861,001-190,865,700 , GRCh37.p13 chr3: 190,578,790-190,583,489 GMNC
    nsv6723630copy number variation1nstd229human GRCh38 chr3: 190,657,017-190,988,806 , GRCh37.p13 chr3: 190,374,806-190,706,595 GMNC, CCT6P4, 4 more genes
    nsv6722505copy number variation1nstd229human GRCh38 chr3: 190,837,001-190,842,000 , GRCh37.p13 chr3: 190,554,790-190,559,789 GMNC
    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
    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
    nsv6296793copy number variation1nstd186human GRCh37 chr3: 190,563,764-190,563,847 , GRCh38.p12 chr3: 190,845,975-190,846,058 GMNC
    nsv6296001copy number variation1nstd186human GRCh37 chr3: 190,560,735-190,560,786 , GRCh38.p12 chr3: 190,842,946-190,842,997 GMNC
    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
    nsv6290259copy number variation1nstd102humanPathogenic GRCh37 chr3: 189,608,636-197,532,175 , GRCh38.p12 chr3: 189,890,847-197,805,304 LINC01972, LINC02026, 174 more genes
    nsv6277974insertion1nstd214human GRCh38 chr3: 190,842,946-190,842,946 , GRCh37.p13 chr3: 190,560,735-190,560,735 GMNC
    nsv6223371insertion1nstd214human GRCh38 chr3: 190,856,485-190,856,485 , GRCh37.p13 chr3: 190,574,274-190,574,274 GMNC
    nsv6160860copy number variation1nstd214human GRCh38 chr3: 190,856,222-190,856,287 , GRCh37.p13 chr3: 190,574,011-190,574,076 GMNC
    nsv6140245copy number variation1nstd206human GRCh38 chr3: 190,842,946-190,842,997 , GRCh37.p13 chr3: 190,560,735-190,560,786 GMNC
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