GENETIC ENCYCLOPEDIA
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GRCh37/hg19 22q13.2(chr22:41590999-41759326)x1 AND not provided

Significance: Uncertain significance
ClinVar: RCV000846905

Variant: GRCh37/hg19 22q13.2(chr22:41590999-41759326)x1

Type: Variant
Allele: GRCh37/hg19 22q13.2(chr22:41590999-41759326)x1 673789
Gene:
Type: copy number loss
Location: Chr22: 41590999 - 41759326 - assembly GRCh37

Condition

Disease: not provided