ClinVar Miner

List of intergenic variants reported as likely pathogenic for Chromosome 17p13.1 deletion syndrome

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP
NCBI36/hg18 17p13.1(chr17:6853665-8107394)x4

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