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Items: 1 to 20 of 227

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7056672inversion1nstd229human GRCh38 chr6: 51,226,717-52,446,371 , GRCh37.p13 chr6: 51,095,293-52,311,169 MIR206, LOC101927082, 16 more genes
    nsv7053224inversion1nstd229human GRCh38 chr6: 52,383,867-53,956,565 , GRCh37.p13 chr6: 52,248,665-53,821,363 RPA3P2, RN7SKP256, 43 more genes
    nsv7039225inversion1nstd229human GRCh38 chr6: 52,383,865-53,974,829 , GRCh37.p13 chr6: 52,248,663-53,839,627 MIR5685, GSTA8P, 43 more genes
    nsv6796990copy number variation1nstd229human GRCh38 chr6: 52,376,131-52,537,280 , GRCh37.p13 chr6: 52,240,929-52,402,078 EFHC1, TRAM2, 1 more genes
    nsv6796784copy number variation1nstd229human GRCh38 chr6: 52,431,957-52,508,995 , GRCh37.p13 chr6: 52,296,755-52,373,793 TRAM2, EFHC1
    nsv6791348copy number variation1nstd229human GRCh38 chr6: 52,487,286-52,487,375 , GRCh37.p13 chr6: 52,352,084-52,352,173 EFHC1
    nsv6786404copy number variation1nstd229human GRCh38 chr6: 52,472,636-52,472,690 , GRCh37.p13 chr6: 52,337,434-52,337,488 EFHC1
    nsv6785147copy number variation1nstd229human GRCh38 chr6: 52,376,212-52,424,955 , GRCh37.p13 chr6: 52,241,010-52,289,753 PAQR8, EFHC1
    nsv6784887copy number variation1nstd229human GRCh38 chr6: 52,455,401-52,462,100 , GRCh37.p13 chr6: 52,320,199-52,326,898 EFHC1
    nsv6779372copy number variation1nstd229human GRCh38 chr6: 52,460,888-52,467,011 , GRCh37.p13 chr6: 52,325,686-52,331,809 EFHC1
    nsv6778362copy number variation1nstd229human GRCh38 chr6: 52,431,602-52,431,718 , GRCh37.p13 chr6: 52,296,400-52,296,516 EFHC1
    nsv6563073inversion1nstd223human GRCh38 chr6: 52,107,269-56,893,586 , GRCh37.p13 chr6: 51,972,067-56,758,384 GSTA1, LOC730101, 79 more genes
    nsv6559089inversion1nstd223human GRCh38 chr6: 52,461,652-52,461,897 , GRCh37.p13 chr6: 52,326,450-52,326,695 EFHC1
    nsv6403250copy number variation1nstd223human GRCh38 chr6: 52,469,046-52,469,604 , GRCh37.p13 chr6: 52,333,844-52,334,402 EFHC1
    nsv6401046copy number variation1nstd223human GRCh38 chr6: 52,438,501-52,440,500 , GRCh37.p13 chr6: 52,303,299-52,305,298 EFHC1
    nsv6314749copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 43,636,308-64,947,206 , GRCh38.p12 chr6: 43,668,571-64,237,313 ACTG1P9, CRISP1, 245 more genes
    nsv6290734copy number variation1nstd102humanUncertain significance GRCh37 chr6: 52,238,224-52,541,279 , GRCh38.p12 chr6: 52,373,426-52,676,481 PAQR8, TRAM2-AS1, 5 more genes
    nsv6185500copy number variation1nstd214human GRCh38 chr6: 52,472,636-52,472,716 , GRCh37.p13 chr6: 52,337,434-52,337,514 EFHC1
    nsv6181404copy number variation1nstd214human GRCh38 chr6: 52,472,636-52,472,689 , GRCh37.p13 chr6: 52,337,434-52,337,487 EFHC1
    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
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