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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6713100copy number variation1nstd229human GRCh38 chr3: 15,359,925-17,364,956 , GRCh37.p13 chr3: 15,401,432-17,406,448 RNU6-1024P, COLQ, 27 more genes
    nsv6712034copy number variation1nstd229human GRCh38 chr3: 14,670,901-15,564,100 , GRCh37.p13 chr3: 14,712,408-15,605,607 COLQ, RNU6-1024P, 22 more genes
    nsv6709093copy number variation1nstd229human GRCh38 chr3: 15,413,746-15,416,501 , GRCh37.p13 chr3: 15,455,253-15,458,008 METTL6
    nsv6704905copy number variation1nstd229human GRCh38 chr3: 15,378,637-15,384,191 , GRCh37.p13 chr3: 15,420,144-15,425,698 METTL6
    nsv6701065copy number variation1nstd229human GRCh38 chr3: 15,374,198-15,381,284 , GRCh37.p13 chr3: 15,415,705-15,422,791 HMGN2P7, METTL6
    nsv6634367copy number variation1nstd102humanPathogenic GRCh37 chr3: 13,836,340-25,357,427 , GRCh38.p12 chr3: 13,794,843-25,315,936 TMEM43, SLC6A6, 132 more genes
    nsv6628286copy number variation1nstd224human GRCh37 chr3: 15,440,556-15,520,486 , GRCh38.p12 chr3: 15,399,049-15,478,979 METTL6, RNU6-1024P, 2 more genes
    nsv6553060inversion1nstd223human GRCh38 chr3: 15,424,075-15,424,175 , GRCh37.p13 chr3: 15,465,582-15,465,682 METTL6
    nsv6362374copy number variation1nstd223human GRCh38 chr3: 15,407,884-15,408,287 , GRCh37.p13 chr3: 15,449,391-15,449,794 METTL6
    nsv6315249copy number variation1nstd102humanPathogenic GRCh38 chr3: 13,371,737-20,095,506 , GRCh37.p13 chr3: 13,413,237-20,136,998 RNU6-905P, PRR3P1, 99 more genes
    nsv6291013copy number variation1nstd102humanUncertain significance GRCh37 chr3: 15,085,863-16,402,392 , GRCh38.p12 chr3: 15,044,356-16,360,885 MIR563, RNU6-1024P, 30 more genes
    nsv6160269copy number variation1nstd214human GRCh38 chr3: 15,413,775-15,413,870 , GRCh37.p13 chr3: 15,455,282-15,455,377 METTL6
    nsv6157263copy number variation1nstd214human GRCh38 chr3: 15,390,813-15,390,906 , GRCh37.p13 chr3: 15,432,320-15,432,413 METTL6
    nsv5991684copy number variation1nstd212human GRCh38 chr3: 15,406,604-15,406,662 , GRCh37.p13 chr3: 15,448,111-15,448,169 METTL6
    nsv5968065inversion1nstd209human GRCh38 chr3: 14,742,874-15,551,121 , GRCh37.p13 chr3: 14,784,381-15,592,628 , NR2C2, 21 more genes
    nsv5892165copy number variation1nstd209human GRCh38 chr3: 15,391,774-15,391,839 , GRCh37.p13 chr3: 15,433,281-15,433,346 METTL6
    nsv5675836mobile element insertion1nstd211human GRCh38 chr3: 15,381,049-15,381,049 , GRCh37.p13 chr3: 15,422,556-15,422,556 METTL6
    nsv5566990copy number variation1nstd207human GRCh38 chr3: 15,390,866-15,390,959 , GRCh37.p13 chr3: 15,432,373-15,432,466 METTL6
    nsv5367006translocation1nstd200human GRCh38 chr3: 15,404,961-15,404,961 , GRCh38 chr5: 174,933,962-174,933,962 , GRCh37.p13 chr5: 174,360,965-174,360,965 , GRCh37.p13 chr3: 15,446,468-15,446,468 METTL6, LINC01951
    nsv5367005translocation1nstd200human GRCh38 chr5: 174,912,745-174,912,745 , GRCh38 chr3: 15,404,546-15,404,546 , GRCh37.p13 chr3: 15,446,053-15,446,053 , GRCh37.p13 chr5: 174,339,748-174,339,748 METTL6
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