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Items: 1 to 20 of 183

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137788copy number variation1nstd102humanPathogenic GRCh37 chr2: 24,601,818-43,466,284 , GRCh38.p12 chr2: 24,378,949-43,239,145 GTF3C2-AS1, MAPRE3-AS1, 316 more genes
    nsv6112680copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 24,881,528-43,460,021 , GRCh38.p12 chr2: 24,658,659-43,232,882 ADCY3, ALK, 314 more genes
    nsv5871887copy number variation1nstd209human GRCh38 chr2: 24,802,012-24,802,158 , GRCh37.p13 chr2: 25,024,881-25,025,027 CENPO
    nsv5720590mobile element insertion1nstd211human GRCh38 chr2: 24,812,304-24,812,304 , GRCh37.p13 chr2: 25,035,173-25,035,173 CENPO
    nsv5565721copy number variation1nstd207human GRCh38 chr2: 24,817,554-24,817,603 , GRCh37.p13 chr2: 25,040,423-25,040,472 ADCY3, CENPO
    nsv5564107mobile element insertion1nstd206human GRCh38 chr2: 24,812,304-24,812,355 , GRCh37.p13 chr2: 25,035,173-25,035,224 CENPO
    nsv5443095copy number variation1nstd206human GRCh38 chr2: 24,819,766-24,819,866 , GRCh37.p13 chr2: 25,042,635-25,042,735 CENPO, ADCY3
    nsv5436984copy number variation1nstd206human GRCh38 chr2: 24,811,110-24,811,764 , GRCh37.p13 chr2: 25,033,979-25,034,633 CENPO
    nsv5288635copy number variation1nstd204human GRCh37.p13 chr2: 25,009,785-25,029,747 , GRCh38.p13 chr2: 24,786,916-24,806,878 CENPO, PTRHD1, 1 more genes
    nsv5218561copy number variation1nstd204human GRCh38.p13 chr2: 24,786,918-24,803,599 , GRCh37.p13 chr2: 25,009,787-25,026,468 LOC105369164, PTRHD1, 1 more genes
    nsv5079992mobile element insertion1nstd203human GRCh38 chr2: 24,808,218-24,808,234 , GRCh37.p13 chr2: 25,031,087-25,031,103 CENPO
    nsv5070757mobile element insertion1nstd203human GRCh38 chr2: 24,798,975-24,799,042 , GRCh37.p13 chr2: 25,021,844-25,021,911 CENPO
    nsv5069012mobile element insertion1nstd203human GRCh38 chr2: 24,799,042-24,799,061 , GRCh37.p13 chr2: 25,021,911-25,021,930 CENPO
    nsv4904859copy number variation1nstd200human GRCh38 chr2: 24,710,616-24,914,385 , GRCh37.p13 chr2: 24,933,485-25,137,254 PTRHD1, LOC105377626, 4 more genes
    nsv4900677copy number variation1nstd200human GRCh38 chr2: 24,811,894-24,812,022 , GRCh37.p13 chr2: 25,034,763-25,034,891 CENPO
    nsv4900676copy number variation1nstd200human GRCh38 chr2: 24,786,920-24,806,877 , GRCh37.p13 chr2: 25,009,789-25,029,746 PTRHD1, LOC105369164, 1 more genes
    nsv4775799copy number variation1nstd200human GRCh37 chr2: 25,034,763-25,034,891 , GRCh38.p12 chr2: 24,811,894-24,812,022 CENPO
    nsv4775798copy number variation1nstd200human GRCh37 chr2: 25,009,789-25,029,746 , GRCh38.p12 chr2: 24,786,920-24,806,877 CENPO, LOC105369164, 1 more genes
    nsv4705208copy number variation1nstd195human GRCh38.p12 chr2: 24,536,832-24,800,432 , GRCh37 chr2: 24,759,701-25,023,301 NCOA1, CENPO, 4 more genes
    nsv4674713copy number variation1nstd102humanUncertain significance GRCh37 chr2: 24,710,112-25,987,357 , GRCh38.p12 chr2: 24,487,243-25,764,488 RN7SL856P, NCOA1, 20 more genes
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