ClinVar

GRCh37/hg19 16p13.3(chr16:2817166-3056563)x3

Genes:

• FLYWCH2:FLYWCH family member 2 [Gene - HGNC]
• FLYWCH1:FLYWCH-type zinc finger 1 [Gene - HGNC]
• ELOB:elongin B [Gene - OMIM - HGNC]
• KREMEN2:kringle containing transmembrane protein 2 [Gene - OMIM - HGNC]
• PAQR4:progestin and adipoQ receptor family member 4 [Gene - OMIM - HGNC]
• PKMYT1:protein kinase, membrane associated tyrosine/threonine 1 [Gene - OMIM - HGNC]
• PRSS21:serine protease 21 [Gene - OMIM - HGNC]
• PRSS22:serine protease 22 [Gene - OMIM - HGNC]
• PRSS33:serine protease 33 [Gene - OMIM - HGNC]
• PRSS41:serine protease 41 [Gene - HGNC]
• SRRM2:serine/arginine repetitive matrix 2 [Gene - OMIM - HGNC]
• ZG16B:zymogen granule protein 16B [Gene - HGNC]

Variant type:

copy number gain

Cytogenetic location:

16p13.3

Genomic location:

Chr16: 2817166 - 3056563 (on Assembly GRCh37)

Preferred name:

GRCh37/hg19 16p13.3(chr16:2817166-3056563)x3

HGVS:

This HGVS expression did not pass validation