ClinVar Miner

List of intergenic variants reported as likely benign by Clinical Cytogenomics Laboratory,Center for Precision Diagnostics, University of Washington

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 2
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HGVS dbSNP
GRCh37/hg19 4q13.1(chr4:60902170-61825240)x1
GRCh37/hg19 Xp22.33(chrX:892049-1425973)x3

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