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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3883724copy number variation1nstd102humanLikely benign GRCh37 chr3: 196,326,784-196,381,502 , GRCh38.p12 chr3: 196,599,913-196,654,631 NRROS, LINC01063
    nsv3915488copy number variation1nstd102humanPathogenic GRCh37 chr3: 185,203,637-197,837,049 , NCBI36 chr3: 186,686,331-199,321,446 , GRCh38 chr3: 185,485,849-198,110,178 NRROS, SNAR-I, 260 more genes
    nsv3920607copy number variation1nstd102humanPathogenic NCBI36 chr3: 187,082,628-197,946,692 , GRCh37.p13 chr3: 185,599,934-196,462,295 , GRCh38.p12 chr3: 185,882,146-196,735,424 NRROS, FGF12, 212 more genes
    nsv3872972copy number variation1nstd102humanPathogenic GRCh37 chr3: 189,101,446-197,838,262 , GRCh38.p12 chr3: 189,383,657-198,111,391 NRROS, TMEM44, 187 more genes
    nsv6290259copy number variation1nstd102humanPathogenic GRCh37 chr3: 189,608,636-197,532,175 , GRCh38.p12 chr3: 189,890,847-197,805,304 NRROS, LINC01972, 174 more genes
    nsv6290248copy number variation1nstd102humanPathogenic GRCh37 chr3: 191,866,466-197,842,171 , GRCh38.p12 chr3: 192,148,677-198,115,300 NRROS, PIGZ, 156 more genes
    nsv3920444copy number variation1nstd102humanPathogenic NCBI36 chr3: 195,540,958-198,905,009 , GRCh38 chr3: 194,338,534-197,693,741 , GRCh37 chr3: 194,059,263-197,420,612 NRROS, RN7SL36P, 107 more genes
    nsv4674423copy number variation1nstd102humanPathogenic GRCh37 chr3: 195,652,973-197,346,971 , GRCh38.p12 chr3: 195,926,102-197,620,100 NRROS, LOC100133326, 54 more genes
    nsv6315456copy number variation1nstd102humanPathogenic GRCh37 chr3: 195,703,615-197,386,180 , GRCh38.p12 chr3: 195,976,744-197,659,309 NRROS, PIGX, 54 more genes
    nsv7098929copy number variation1nstd102humanPathogenic GRCh38 chr3: 195,950,438-197,629,463 , GRCh37.p13 chr3: 195,677,309-197,356,334 NRROS, LINC01063, 52 more genes
    nsv3886526copy number variation1nstd102humanPathogenic GRCh37 chr3: 195,690,227-197,356,334 , GRCh38.p12 chr3: 195,963,356-197,629,463 NRROS, BDH1, 52 more genes
    nsv6636887copy number variation1nstd102humanPathogenic GRCh37 chr3: 195,690,228-197,356,334 , GRCh38.p12 chr3: 195,963,357-197,629,463 NRROS, LOC105374307, 52 more genes
    nsv3875183copy number variation1nstd102humanPathogenic GRCh37 chr3: 195,725,402-197,386,693 , GRCh38.p12 chr3: 195,998,531-197,659,822 NRROS, TM4SF19-DYNLT2B, 52 more genes
    nsv3924895copy number variation1nstd102humanPathogenic NCBI36 chr3: 197,185,595-198,845,618 , GRCh37.p13 chr3: 195,701,198-197,361,221 , GRCh38.p12 chr3: 195,974,327-197,634,350 NRROS, LOC101926923, 53 more genes
    nsv3911432copy number variation1nstd102humanPathogenic NCBI36 chr3: 197,188,012-198,840,731 , GRCh38 chr3: 195,976,744-197,629,463 , GRCh37 chr3: 195,703,615-197,356,334 NRROS, LOC101926923, 52 more genes
    nsv3872813copy number variation1nstd102humanPathogenic GRCh37 chr3: 195,703,615-197,348,575 , GRCh38.p12 chr3: 195,976,744-197,621,704 NRROS, SDHAP4, 52 more genes
    nsv3921980copy number variation1nstd102humanPathogenic NCBI36 chr3: 197,166,979-198,809,180 , GRCh37 chr3: 195,682,582-197,324,783 , GRCh38 chr3: 195,955,711-197,597,912 NRROS, LINC01063, 51 more genes
    nsv3879998copy number variation1nstd102humanPathogenic GRCh38 chr3: 195,990,063-197,617,301 , GRCh37.p13 chr3: 195,716,934-197,344,172 NRROS, MIR4797, 52 more genes
    nsv3914020copy number variation1nstd102humanPathogenic GRCh37 chr3: 195,701,162-197,324,783 , GRCh38 chr3: 195,974,291-197,597,912 , NCBI36 chr3: 197,185,559-198,809,180 NRROS, FBXO45, 51 more genes
    nsv3916750copy number variation1nstd102humanPathogenic NCBI36 chr3: 197,247,045-198,869,808 , GRCh38 chr3: 196,035,777-197,658,540 , GRCh37 chr3: 195,762,648-197,385,411 NRROS, LOC105374308, 52 more genes
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