ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 4
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HGVS dbSNP
NC_000017.9:g.6838295_7991364del1153070
NC_000017.9:g.6936148_7177360del241213
NC_000017.9:g.6996378_7152828del156451
NC_000017.9:g.7033635_7977678del944044

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