M2342 AND nstd157 - dbVar - NCBI

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Number of Variants: 13

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3318841	copy number variation	6	nstd157	human		GRCh37 chr10: 68,075,032-68,114,481 , GRCh38.p12 chr10: 66,315,274-66,354,723	CTNNA3
nsv3317351	copy number variation	1	nstd157	human		GRCh37 chr2: 29,379,836-29,393,231 , GRCh38.p12 chr2: 29,156,970-29,170,365	CLIP4
nsv3318516	copy number variation	22	nstd157	human		GRCh37 chr13: 64,225,427-64,236,288 , GRCh38.p12 chr13: 63,651,294-63,662,155	LOC105370236
nsv3317763	copy number variation	17	nstd157	human		GRCh37 chr18: 66,746,208-66,755,736 , GRCh38.p12 chr18: 69,078,971-69,088,499	CCDC102B
nsv3318419	copy number variation	1	nstd157	human		GRCh37 chr19: 4,841,151-4,848,593 , GRCh38.p12 chr19: 4,841,139-4,848,581	PLIN3
nsv3317717	copy number variation	26	nstd157	human		GRCh37 chr12: 43,021,431-43,026,485 , GRCh38.p12 chr12: 42,627,629-42,632,683	LINC02402
nsv3318709	copy number variation	2	nstd157	human		GRCh37 chr17: 44,173,505-44,189,067 , GRCh38.p12 chr17: 46,096,139-46,111,701 , GRCh38.p12 chr17\|NT_187663.1: 798,245-813,800	KANSL1
nsv3318661	copy number variation	1	nstd157	human		GRCh37 chr11: 107,940,546-108,040,484 , GRCh38.p12 chr11: 108,069,819-108,169,757	ACAT1, NPAT, 1 more genes
nsv3318316	copy number variation	72	nstd157	human		GRCh37 chr14: 41,615,868-41,661,685 , GRCh38.p12 chr14: 41,146,665-41,192,482	0
nsv3318478	copy number variation	26	nstd157	human		GRCh37 chr7: 62,149,006-62,162,385 , GRCh38.p12 chr7: 62,688,628-62,702,007	0
nsv3318135	copy number variation	2	nstd157	human		GRCh38.p12 chr6: 31,391,178-31,485,887 , GRCh37 chr6: 31,358,955-31,453,664	HCP5, HLA-X, 5 more genes
nsv3318204	copy number variation	2	nstd157	human		GRCh37 chr11: 37,768,477-37,839,784 , GRCh38.p12 chr11: 37,746,927-37,818,234	0
nsv3318370	copy number variation	14	nstd157	human		GRCh37 chr18: 63,200,484-63,206,335 , GRCh38.p12 chr18: 65,533,248-65,539,099	0

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