GENETIC ENCYCLOPEDIA
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GRCh37/hg19 6p22.1-q14.1(chr6:29455465-81447367) AND not provided

Significance: Pathogenic
ClinVar: RCV000767714

Variant: GRCh37/hg19 6p22.1-q14.1(chr6:29455465-81447367)

Type: Variant
Allele: GRCh37/hg19 6p22.1-q14.1(chr6:29455465-81447367) 614010
Gene:
Type: copy number gain
Location: Chr6: 29455465 - 81447367 - assembly GRCh37

Condition

Disease: not provided