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Items: 1 to 20 of 384

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6125382copy number variation1nstd186human GRCh37 chr17: 74,786,248-74,790,868 , GRCh38.p12 chr17: 76,790,166-76,794,786 MFSD11
    nsv5978319insertion1nstd209human GRCh38 chr17: 76,755,812-76,755,812 , GRCh37.p13 chr17: 74,751,894-74,751,894 MFSD11
    nsv5942366copy number variation1nstd209human GRCh38 chr17: 76,770,720-76,774,124 , GRCh37.p13 chr17: 74,766,802-74,770,206 MFSD11
    nsv5941715copy number variation1nstd209human GRCh38 chr17: 76,787,243-76,792,225 , GRCh37.p13 chr17: 74,783,325-74,788,307 MFSD11
    nsv5941205copy number variation1nstd209human GRCh38 chr17: 76,768,847-76,768,919 , GRCh37.p13 chr17: 74,764,929-74,765,001 MFSD11
    nsv5937120copy number variation1nstd209human GRCh38 chr17: 76,743,234-76,743,284 , GRCh37.p13 chr17: 74,739,316-74,739,366 MFSD11
    nsv5927753copy number variation1nstd209human GRCh38 chr17: 76,790,445-76,794,795 , GRCh37.p13 chr17: 74,786,527-74,790,877 MFSD11
    nsv5887495copy number variation1nstd209human GRCh38 chr17: 76,790,293-76,792,232 , GRCh37.p13 chr17: 74,786,375-74,788,314 MFSD11
    nsv5886846copy number variation1nstd209human GRCh38 chr17: 76,774,784-76,776,033 , GRCh37.p13 chr17: 74,770,866-74,772,115 MFSD11
    nsv5882128copy number variation1nstd209human GRCh38 chr17: 76,792,033-76,794,792 , GRCh37.p13 chr17: 74,788,115-74,790,874 MFSD11
    nsv5879572copy number variation1nstd209human GRCh38 chr17: 76,787,292-76,791,592 , GRCh37.p13 chr17: 74,783,374-74,787,674 MFSD11
    nsv5873488copy number variation1nstd209human GRCh38 chr17: 76,770,734-76,774,133 , GRCh37.p13 chr17: 74,766,816-74,770,215 MFSD11
    nsv5600820copy number variation1nstd207human GRCh38 chr17: 76,787,243-76,792,225 , GRCh37.p13 chr17: 74,783,325-74,788,307 MFSD11
    nsv5563569sequence alteration1nstd206human GRCh37.p13 chr17: 74,682,310-74,791,072 , GRCh38 chr17: 76,686,228-76,794,990 SRSF2, JMJD6, 6 more genes
    nsv5538886insertion1nstd206human GRCh38 chr17: 76,761,450-76,761,501 , GRCh37.p13 chr17: 74,757,532-74,757,583 MFSD11
    nsv5525440copy number variation1nstd206human GRCh38 chr17: 76,768,850-76,768,920 , GRCh37.p13 chr17: 74,764,932-74,765,002 MFSD11
    nsv5522916copy number variation1nstd206human GRCh38 chr17: 76,790,166-76,794,786 , GRCh37.p13 chr17: 74,786,248-74,790,868 MFSD11
    nsv5393071copy number variation1nstd186human GRCh37 chr17: 74,786,580-74,790,869 , GRCh38.p12 chr17: 76,790,498-76,794,787 MFSD11
    nsv5392794copy number variation1nstd186human GRCh37 chr17: 74,786,585-74,790,868 , GRCh38.p12 chr17: 76,790,503-76,794,786 MFSD11
    nsv5390642copy number variation1nstd186human GRCh37 chr17: 74,783,361-74,788,268 , GRCh38.p12 chr17: 76,787,279-76,792,186 MFSD11
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