M2220 AND nstd157 - dbVar - NCBI

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Number of Variants: 12

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3318177	copy number variation	1	nstd157	human		GRCh37 chr11: 81,841,736-82,023,512 , GRCh38.p12 chr11: 82,130,694-82,312,470	MIR4300HG
nsv3318967	copy number variation	3	nstd157	human		GRCh37 chr5: 3,958,271-3,970,470 , GRCh38.p12 chr5: 3,958,157-3,970,356	LOC105374626
nsv3317770	copy number variation	9	nstd157	human		GRCh37 chr8: 15,401,929-15,411,867 , GRCh38.p12 chr8: 15,544,420-15,554,358	TUSC3
nsv3318145	copy number variation	6	nstd157	human		GRCh37 chr4: 39,705,484-39,713,134 , GRCh38.p12 chr4: 39,703,864-39,711,514	UBE2K
nsv3317745	copy number variation	1	nstd157	human		GRCh38.p12 chr19: 7,457,873-7,480,792 , GRCh37 chr19: 7,522,759-7,545,678	ARHGEF18, PEX11G
nsv3318410	copy number variation	1	nstd157	human		GRCh38.p12 chr10: 94,759,374-94,779,387 , GRCh37 chr10: 96,519,131-96,539,144	CYP2C19, MTND4P19
nsv3318884	copy number variation	1	nstd157	human		GRCh38.p12 chr9: 90,522,023-90,732,914 , GRCh37 chr9: 93,284,305-93,495,196	DIRAS2, LINC01501
nsv3317077	copy number variation	1	nstd157	human		GRCh38.p12 chr12: 63,823,237-63,858,312 , GRCh37 chr12: 64,217,017-64,252,092	SRGAP1, PABPC1P4, 1 more genes
nsv3317859	copy number variation	29	nstd157	human		GRCh37 chr4: 64,136,609-64,154,477 , GRCh38.p12 chr4: 63,270,891-63,288,759	0
nsv3318308	copy number variation	19	nstd157	human		GRCh37 chr16: 19,945,540-19,962,636 , GRCh38.p12 chr16: 19,934,218-19,951,314	0
nsv3317878	copy number variation	25	nstd157	human		GRCh37 chr3: 162,131,408-162,142,475 , GRCh38.p12 chr3: 162,413,620-162,424,687	0
nsv3317496	copy number variation	1	nstd157	human		GRCh37 chr3: 128,404,269-128,412,024 , GRCh38.p12 chr3: 128,685,426-128,693,181	0

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