GENETIC ENCYCLOPEDIA
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GRCh37/hg19 2p25.3(chr2:15672-657652)x1 AND not provided

Significance: Likely benign
ClinVar: RCV000752803

Variant: GRCh37/hg19 2p25.3(chr2:15672-657652)x1

Type: Variant
Allele: GRCh37/hg19 2p25.3(chr2:15672-657652)x1 607503
Gene:
Type: copy number loss
Location: Chr2: 15672 - 657652 - assembly GRCh37

Condition

Disease: not provided