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Items: 1 to 20 of 191

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5925954copy number variation1nstd209human GRCh38 chr6: 166,585,488-166,586,677 , GRCh37.p13 chr6: 166,998,976-167,000,165 RPS6KA2, RAMACL
    nsv5584139copy number variation1nstd207human GRCh38 chr6: 166,585,488-166,586,677 , GRCh37.p13 chr6: 166,998,976-167,000,165 RPS6KA2, RAMACL
    nsv5460775copy number variation1nstd206human GRCh38 chr6: 166,585,502-166,586,678 , GRCh37.p13 chr6: 166,998,990-167,000,166 RAMACL, RPS6KA2
    nsv5325419translocation1nstd204human GRCh37.p13 chr6: 167,000,166-167,000,166 , GRCh37.p13 chr6: 166,998,990-166,998,990 , GRCh38.p13 chr6: 166,585,502-166,585,502 , GRCh38.p13 chr6: 166,586,678-166,586,678 RPS6KA2, RAMACL
    nsv5224368copy number variation1nstd204human GRCh38.p13 chr6: 166,585,501-166,586,700 , GRCh37.p13 chr6: 166,998,989-167,000,188 RPS6KA2, RAMACL
    nsv4965935copy number variation1nstd200human GRCh38 chr6: 166,585,502-166,586,678 , GRCh37.p13 chr6: 166,998,990-167,000,166 RPS6KA2, RAMACL
    nsv4818044copy number variation1nstd200human GRCh37 chr6: 166,998,990-167,000,166 , GRCh38.p12 chr6: 166,585,502-166,586,678 RAMACL, RPS6KA2
    nsv4729645copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 166,083,476-170,919,482 , GRCh38.p12 chr6: 165,669,988-170,610,394 CCR6, GNG5P1, 118 more genes
    nsv4708666copy number variation3nstd195human GRCh37 chr6: 166,998,976-166,998,977 , GRCh38.p12 chr6: 166,585,488-166,585,489 RPS6KA2, RAMACL
    nsv4675923copy number variation1nstd102humanPathogenic GRCh37 chr6: 162,452,035-170,919,482 , GRCh38.p12 chr6: 162,031,003-170,610,394 TRE-TTC15-1, LOC105378137, 148 more genes
    nsv4675843copy number variation1nstd102humanUncertain significance GRCh37 chr6: 166,827,923-167,156,755 , GRCh38.p12 chr6: 166,414,435-166,743,267 RAMACL, RPS6KA2-IT1, 4 more genes
    nsv4675281copy number variation1nstd102humanPathogenic GRCh37 chr6: 162,661,108-170,919,482 , GRCh38.p12 chr6: 162,240,076-170,610,394 LOC105378127, LOC105378130, 148 more genes
    nsv4652239copy number variation3nstd186human GRCh37 chr6: 166,998,990-167,000,166 , GRCh38.p12 chr6: 166,585,502-166,586,678 RPS6KA2, RAMACL
    nsv4606266copy number variation1nstd183human GRCh37 chr6: 166,999,036-167,000,159 , GRCh38.p12 chr6: 166,585,548-166,586,671 RPS6KA2, RAMACL
    nsv4523721copy number variation1nstd166human GRCh37.p13 chr6: 166,998,990-167,000,166 , GRCh38.p12 chr6: 166,585,502-166,586,678 RAMACL, RPS6KA2
    nsv4455397copy number variation1nstd102humanPathogenic GRCh37 chr6: 166,607,593-170,919,482 , GRCh38.p12 chr6: 166,194,105-170,610,394 TBP, LOC112267970, 108 more genes
    nsv4436131complex substitution1nstd102humanPathogenic GRCh38.p12 chr6: 151,122,197-170,745,979 , GRCh37 chr6: 151,443,333-171,115,067 ACAT2, CCR6, 303 more genes
    nsv4404049copy number variation1nstd174human GRCh37 chr6: 166,998,381-167,000,738 , GRCh38.p12 chr6: 166,584,893-166,587,250 RPS6KA2, RAMACL
    nsv4382786copy number variation1nstd173human GRCh37 chr6: 166,963,233-167,011,549 , GRCh38.p12 chr6: 166,549,745-166,598,061 RAMACL, RPS6KA2
    nsv4376081copy number variation1nstd173human GRCh37 chr6: 163,617,482-170,919,482 , GRCh38.p12 chr6: 163,196,450-170,610,394 , LOC107986550, 151 more genes
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