ClinVar Miner

List of variants reported as likely pathogenic for Chromosome Xq26.3 duplication syndrome

Minimum submission review status: Collection method:
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ClinVar version:
Total variants: 4
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HGVS dbSNP
NC_000023.10:g.135533330_136123779dup
NC_000023.10:g.135549274_136126345dup
NC_000023.10:g.135596446_136254970dup
NC_000023.10:g.135622314_136191699dup

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