ClinVar Miner

List of variants reported as pathogenic for syndrome caused by partial chromosomal deletion by Department of Genetics, Fundacion Jimenez Diaz University Hospital

Included ClinVar conditions (110):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 2
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HGVS dbSNP gnomAD frequency
GRCh37/hg19 11p14.1-13(chr11:29750813-32752091)x1
GRCh37/hg19 11p15.1-13(chr11:21586131-33168232)x1

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