Hs06421125_cn

• Gene Symbol: MYHAS
• Assay Reference Genome Location: Chr.17:10383224 on build GRCh38
• Cytoband: 17p13.1

Target Gene Details

• Entrez Gene ID: 100128560
• Gene Name: myosin heavy chain gene cluster antisense RNA
• Gene Aliases: -
• Location: Chr.17:10383132-10625540 on Build GRCh38
• Assay Gene Location: Overlaps Exon 1 - Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
MYHAS	NR_125367.1
	AK097500.1
	BX107674.1

Target Copy Number Variation Details

• DGV Version: Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
dgv5443n54	Chr.17:10090245 - 10512523 on Build GRCh38	Gain	GAS7 MYH4 MYH1 MYH8 MYHAS MYH13
nsv574349	Chr.17:10320967 - 10392180 on Build GRCh38	Loss	MYH8 MYHAS MYH13
dgv3098n100	Chr.17:10330021 - 10388502 on Build GRCh38	Loss	MYHAS MYH13
nsv520771	Chr.17:10073260 - 10527958 on Build GRCh38	Gain+Loss	MYH2 GAS7 MYH4 MYH1 MYH8 MYHAS MYH13
nsv1060957	Chr.17:10086444 - 10511479 on Build GRCh38	Gain	GAS7 MYH4 MYH1 MYH8 MYHAS MYH13
nsv833366	Chr.17:10351506 - 10501771 on Build GRCh38	Gain	MYH4 MYH1 MYH8 MYHAS MYH13
nsv574350	Chr.17:10325498 - 10458952 on Build GRCh38	Gain	MYH4 MYH8 MYHAS MYH13
nsv1058835	Chr.17:10322963 - 10939602 on Build GRCh38	Loss	MYH2 TMEM220 MYH4 MYH8 MYHAS MYH3 MAGOH2P TMEM220-AS1 PIRT MYH1 LINC00675 ADPRM MYH13 SCO1

More Information

Additional Information:

For this assay, SNP(s) [rs73273779] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

• Set Membership: Intragenic, Non-exonic, DGV Variation