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Items: 1 to 20 of 159

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097330copy number variation1nstd102humanPathogenic GRCh37 chr6: 39,874,133-39,902,156 , GRCh38.p12 chr6: 39,906,357-39,934,417 LOC102723789, MOCS1
    nsv7093281copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 39,877,645-39,878,462 , GRCh38 chr6: 39,909,901-39,910,718 MOCS1
    nsv7043293inversion1nstd229human GRCh38 chr6: 39,854,165-43,261,822 , GRCh37.p13 chr6: 39,821,941-43,229,560 RPL23P6, RPL32P15, 95 more genes
    nsv6796863copy number variation1nstd229human GRCh38 chr6: 39,919,790-39,922,166 , GRCh37.p13 chr6: 39,887,534-39,889,910 MOCS1
    nsv6795442copy number variation1nstd229human GRCh38 chr6: 39,085,006-40,306,101 , GRCh37.p13 chr6: 39,052,782-40,273,840 GLP1R, E2F4P1, 18 more genes
    nsv6795080copy number variation1nstd229human GRCh38 chr6: 39,926,790-39,930,781 , GRCh37.p13 chr6: 39,894,529-39,898,520 MOCS1
    nsv6793670copy number variation1nstd229human GRCh38 chr6: 39,905,999-39,906,091 , GRCh37.p13 chr6: 39,873,775-39,873,867 MOCS1
    nsv6787874copy number variation1nstd229human GRCh38 chr6: 39,923,090-39,927,258 , GRCh37.p13 chr6: 39,890,834-39,894,997 MOCS1
    nsv6782663copy number variation1nstd229human GRCh38 chr6: 39,866,093-40,138,119 , GRCh37.p13 chr6: 39,833,869-40,105,858 MOCS1, DAAM2-AS1, 4 more genes
    nsv6631059copy number variation1nstd224human GRCh37 chr6: 39,881,120-39,898,993 , GRCh38.p12 chr6: 39,913,376-39,931,254 MOCS1
    nsv6399688copy number variation1nstd223human GRCh38 chr6: 39,866,093-40,138,119 , GRCh37.p13 chr6: 39,833,869-40,105,858 RPL23P6, LOC102723789, 4 more genes
    nsv6312578copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 39,895,048-39,895,317 , GRCh38.p12 chr6: 39,927,309-39,927,578 MOCS1
    nsv6312577copy number variation1nstd102humanUncertain significance GRCh37 chr6: 39,877,569-39,902,156 , GRCh38.p12 chr6: 39,909,825-39,934,417 LOC102723789, MOCS1
    nsv6312013copy number variation1nstd102humanLikely benign GRCh38 chr6: 39,916,235-39,916,236 , GRCh37 chr6: 39,883,979-39,883,980 MOCS1
    nsv6280577insertion1nstd214human GRCh38 chr6: 39,906,030-39,906,030 , GRCh37.p13 chr6: 39,873,806-39,873,806 MOCS1
    nsv6168752copy number variation1nstd214human GRCh38 chr6: 39,909,199-39,909,296 , GRCh37.p13 chr6: 39,876,975-39,877,040 MOCS1
    nsv6135921copy number variation1nstd213human GRCh37 chr6: 34,700,000-52,650,001 , GRCh38.p12 chr6: 34,732,223-52,785,203 ACTG1P9, CRISP1, 361 more genes
    nsv6079225insertion1nstd212human GRCh38 chr6: 39,906,005-39,906,005 , GRCh37.p13 chr6: 39,873,781-39,873,781 MOCS1
    nsv6062253insertion1nstd212human GRCh38 chr6: 39,926,750-39,926,750 , GRCh37.p13 chr: NaN-NaN MOCS1
    nsv6004085copy number variation1nstd212human GRCh38 chr6: 39,909,266-39,909,330 , GRCh37.p13 chr6: 39,877,010-39,877,074 MOCS1
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