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Items: 1 to 20 of 196

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6793881copy number variation1nstd229human GRCh38 chr6: 44,213,339-44,213,490 , GRCh37.p13 chr6: 44,181,076-44,181,227 MYMX
    nsv6790652copy number variation1nstd229human GRCh38 chr6: 44,204,716-44,209,269 , GRCh37.p13 chr6: 44,172,453-44,177,006 MYMX, RN7SL811P
    nsv6789042copy number variation1nstd229human GRCh38 chr6: 44,187,401-44,191,800 , GRCh37.p13 chr6: 44,155,138-44,159,537 LOC105375072, MYMX
    nsv6788779copy number variation1nstd229human GRCh38 chr6: 44,217,191-44,323,601 , GRCh37.p13 chr6: 44,184,928-44,291,338 TMEM151B, TCTE1, 7 more genes
    nsv6788317copy number variation1nstd229human GRCh38 chr6: 44,191,677-44,193,324 , GRCh37.p13 chr6: 44,159,414-44,161,061 MYMX
    nsv6787193copy number variation1nstd229human GRCh38 chr6: 44,181,401-44,326,600 , GRCh37.p13 chr6: 44,149,138-44,294,337 TMEM151B, AARS2, 10 more genes
    nsv6786949copy number variation1nstd229human GRCh38 chr6: 44,199,322-44,200,440 , GRCh37.p13 chr6: 44,167,059-44,168,177 MYMX
    nsv6781073copy number variation1nstd229human GRCh38 chr6: 44,217,309-44,217,421 , GRCh37.p13 chr6: 44,185,046-44,185,158 MYMX
    nsv6571806inversion1nstd223human GRCh38 chr6: 44,213,312-44,213,537 , GRCh37.p13 chr6: 44,181,049-44,181,274 MYMX
    nsv6571276inversion1nstd223human GRCh38 chr6: 44,213,135-44,213,660 , GRCh37.p13 chr6: 44,180,872-44,181,397 MYMX
    nsv6563727inversion1nstd223human GRCh38 chr6: 44,196,880-44,198,547 , GRCh37.p13 chr6: 44,164,617-44,166,284 MYMX
    nsv6561260inversion1nstd223human GRCh38 chr6: 44,197,249-44,198,177 , GRCh37.p13 chr6: 44,164,986-44,165,914 MYMX
    nsv6407269copy number variation1nstd223human GRCh38 chr6: 44,213,339-44,213,490 , GRCh37.p13 chr6: 44,181,076-44,181,227 MYMX
    nsv6404409copy number variation1nstd223human GRCh38 chr6: 44,207,390-44,210,095 , GRCh37.p13 chr6: 44,175,127-44,177,832 MYMX, RN7SL811P
    nsv6402614copy number variation1nstd223human GRCh38 chr6: 44,199,322-44,200,440 , GRCh37.p13 chr6: 44,167,059-44,168,177 MYMX
    nsv6401590copy number variation1nstd223human GRCh38 chr6: 44,195,514-44,199,758 , GRCh37.p13 chr6: 44,163,251-44,167,495 MYMX
    nsv6400722copy number variation1nstd223human GRCh38 chr6: 44,196,910-44,197,381 , GRCh37.p13 chr6: 44,164,647-44,165,118 MYMX
    nsv6399589copy number variation1nstd223human GRCh38 chr6: 44,210,040-44,213,444 , GRCh37.p13 chr6: 44,177,777-44,181,181 MYMX, RN7SL811P
    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
    nsv6178524copy number variation1nstd214human GRCh38 chr6: 44,213,339-44,213,489 , GRCh37.p13 chr6: 44,181,076-44,181,226 MYMX
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