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Items: 3

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    Number of Variants: 3

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv1791728copy number variation1estd186humanLikely pathogenic GRCh37 (hg19) chr1: 7,101,726-7,256,822 , NCBI36 (hg18) chr1: 7,024,313-7,179,409 , GRCh38 (hg38) chr1: 7,041,666-7,196,762 CAMTA1
    esv1791727copy number variation1estd186humanLikely pathogenic GRCh37 (hg19) chr1: 6,941,117-7,525,200 , NCBI36 (hg18) chr1: 6,863,704-7,447,787 , GRCh38 (hg38) chr1: 6,881,057-7,465,140 CAMTA1
    esv1791726copy number variation1estd186humanLikely pathogenic GRCh37 (hg19) chr1: 6,848,878-6,912,597 , NCBI36 (hg18) chr1: 6,771,465-6,835,184 , GRCh38 (hg38) chr1: 6,788,818-6,852,537 CAMTA1
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