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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
    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
    nsv6730456copy number variation1nstd229human GRCh38 chr3: 193,968,301-194,014,000 , GRCh37.p13 chr3: 193,686,090-193,731,789 LINC02026, LINC02028, 1 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
    nsv6730094copy number variation1nstd229human GRCh38 chr3: 193,933,092-194,041,100 , GRCh37.p13 chr3: 193,650,881-193,758,889 DPPA2P3, LOC105374287, 2 more genes
    nsv6729370copy number variation1nstd229human GRCh38 chr3: 193,992,848-194,027,608 , GRCh37.p13 chr3: 193,710,637-193,745,397 LINC02028, LINC02026, 1 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
    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
    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
    nsv6134833copy number variation1nstd213human GRCh37 chr3: 186,910,000-193,810,001 , GRCh38.p12 chr3: 187,192,212-194,092,212 BCL6, LPP, 85 more genes
    nsv6074655insertion1nstd212human GRCh38 chr3: 193,992,925-193,992,925 , GRCh37.p13 chr3: 193,710,714-193,710,714 DPPA2P3, LINC02026
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv4436392copy number variation1nstd102humanPathogenic GRCh37 chr3: 188,386,566-197,838,262 , GRCh38.p12 chr3: 188,668,778-198,111,391 PPP1R2, GCNT1P3, 194 more genes
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv3924195copy number variation1nstd102humanPathogenic GRCh38 chr3: 193,704,605-198,125,115 , NCBI36 chr3: 194,905,088-199,336,383 , GRCh37 chr3: 193,422,394-197,851,986 LOC105374298, LINC01983, 139 more genes
    nsv3922385copy number variation1nstd102humanPathogenic NCBI36 chr3: 177,369,007-199,329,651 , GRCh37 chr3: 175,886,313-197,845,254 , GRCh38 chr3: 176,168,525-198,118,383 LINC02053, RTP4, 414 more genes
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