GENETIC ENCYCLOPEDIA
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GRCh37/hg19 9q34.2(chr9:135940490-135962157)x3 AND See cases

Significance: Benign/Likely benign
ClinVar: RCV000446639

Variant: GRCh37/hg19 9q34.2(chr9:135940490-135962157)x3

Type: Variant
Allele: GRCh37/hg19 9q34.2(chr9:135940490-135962157)x3 382209
Gene:
Type: copy number gain
Location: Chr9: 135940490 - 135962157 - assembly GRCh37
References: dbVar: nsv2777153
dbVar: nssv13656425
dbVar: nssv13655823
dbVar: nssv13655788
dbVar: nssv13655499
dbVar: nssv13652808
dbVar: nssv13649562
dbVar: nssv13646335
dbVar: nssv13645862
dbVar: nssv13644368
dbVar: nssv13643992
dbVar: nssv13641727
dbVar: nssv13640673

Condition

PhenotypeInstruction: See cases