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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148072copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 193,343,827-194,599,635 , GRCh38.p12 chr3: 193,626,038-194,878,906 CPN2, GP5, 36 more genes
    nsv7040982inversion1nstd229human GRCh38 chr3: 193,802,086-196,241,826 , GRCh37.p13 chr3: 193,519,875-195,968,697 CPN2, RNU6ATAC24P, 73 more genes
    nsv6737289copy number variation1nstd229human GRCh38 chr3: 194,300,984-194,316,282 , GRCh37.p13 chr3: 194,018,773-194,034,071 LINC00887
    nsv6736947copy number variation1nstd229human GRCh38 chr3: 194,292,714-194,303,020 , GRCh37.p13 chr3: 194,010,503-194,020,809 LINC00887
    nsv6736543copy number variation1nstd229human GRCh38 chr3: 194,217,201-194,382,500 , GRCh37.p13 chr3: 193,934,990-194,103,229 LINC02048, LINC02037, 4 more genes
    nsv6733943copy number variation1nstd229human GRCh38 chr3: 194,293,947-194,302,076 , GRCh37.p13 chr3: 194,011,736-194,019,865 LINC00887
    nsv6731714copy number variation1nstd229human GRCh38 chr3: 192,378,501-195,488,100 , GRCh37.p13 chr3: 192,096,290-195,214,903 LSG1, MB21D2, 61 more genes
    nsv6730192copy number variation1nstd229human GRCh38 chr3: 193,965,801-194,389,700 , GRCh37.p13 chr3: 193,683,590-194,110,429 LINC02048, CPN2, 11 more genes
    nsv6727962copy number variation1nstd229human GRCh38 chr3: 194,215,451-194,451,362 , GRCh37.p13 chr3: 193,933,240-194,172,091 LRRC15, LINC02036, 6 more genes
    nsv6725049copy number variation1nstd229human GRCh38 chr3: 194,290,935-194,299,260 , GRCh37.p13 chr3: 194,008,724-194,017,049 LINC00887, LINC02048
    nsv6718526copy number variation1nstd229human GRCh38 chr3: 194,310,593-194,328,775 , GRCh37.p13 chr3: 194,028,382-194,049,504 LINC00887
    nsv6718222copy number variation1nstd229human GRCh38 chr3: 194,179,860-194,436,927 , GRCh37.p13 chr3: 193,897,649-194,157,656 GP5, LINC02048, 6 more genes
    nsv6636634copy number variation1nstd102humanUncertain significance GRCh37 chr3: 193,396,762-195,009,038 , GRCh38.p12 chr3: 193,678,973-195,288,309 LINC02036, LINC02026, 45 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
    nsv6628551copy number variation1nstd224human GRCh37 chr3: 193,855,650-194,188,614 , GRCh38.p12 chr3: 194,137,861-194,467,885 LINC02036, LOC107986172, 9 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
    nsv6313865copy number variation1nstd102humanUncertain significance GRCh37 chr3: 193,836,939-194,169,926 , GRCh38.p12 chr3: 194,119,150-194,449,197 ATP13A3, CPN2, 10 more genes
    nsv6313527copy number variation1nstd102humanUncertain significance GRCh37 chr3: 192,607,378-194,745,252 , GRCh38.p12 chr3: 192,889,589-195,024,523 LINC02036, HES1, 48 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
    nsv6290248copy number variation1nstd102humanPathogenic GRCh37 chr3: 191,866,466-197,842,171 , GRCh38.p12 chr3: 192,148,677-198,115,300 PIGZ, LOC107986173, 156 more genes
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