M2501 AND nstd157 - dbVar - NCBI

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Number of Variants: 18

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3318254	copy number variation	26	nstd157	human		GRCh37 chr13: 69,247,022-69,267,981 , GRCh38.p12 chr13: 68,672,890-68,693,849	RN7SL761P
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
nsv3318029	copy number variation	27	nstd157	human		GRCh37 chr18: 41,976,831-41,982,102 , GRCh38.p12 chr18: 44,396,866-44,402,137	LINC01478
nsv3317666	copy number variation	21	nstd157	human		GRCh37 chr21: 10,715,343-10,883,039 , GRCh38.p12 chr21: 10,629,418-10,797,114	IGHV1OR21-1
nsv3318373	copy number variation	3	nstd157	human		GRCh37 chr7: 156,298,698-156,313,666 , GRCh38.p12 chr7: 156,506,004-156,520,972	RNF32-DT, LOC112268012
nsv3317376	copy number variation	2	nstd157	human		GRCh38.p12 chr16: 155,036-162,650 , GRCh37 chr16: 205,035-212,649	HBZP1, LOC107983982
nsv3318220	copy number variation	21	nstd157	human		GRCh38.p12 chr19: 20,418,529-20,532,427 , GRCh37 chr19: 20,601,335-20,715,233	ZNF826P, ZNF737, 3 more genes
nsv3318745	copy number variation	44	nstd157	human		GRCh37 chr17: 34,438,753-34,483,342 , GRCh38.p12 chr17: 36,111,360-36,155,969 , GRCh38.p12 chr17\|NT_187661.1: 65,457-110,066 , GRCh38.p12 chr17\|NT_187614.1: 346,281-390,870	LOC100419980, LOC101927369, 2 more genes
nsv3318427	copy number variation	34	nstd157	human		GRCh37 chr11: 81,501,218-81,517,261 , GRCh38.p12 chr11: 81,790,176-81,806,219	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
nsv3318380	copy number variation	3	nstd157	human		GRCh37 chr6: 78,326,093-78,334,631 , GRCh38.p12 chr6: 77,616,376-77,624,914	0
nsv3318502	copy number variation	31	nstd157	human		GRCh37 chr9: 78,004,378-78,011,616 , GRCh38.p12 chr9: 75,389,462-75,396,700	0
nsv3318612	copy number variation	2	nstd157	human		GRCh37 chr5: 52,670,932-52,677,265 , GRCh38.p12 chr5: 53,375,102-53,381,435	0
nsv3318900	copy number variation	17	nstd157	human		GRCh37 chr7: 86,940,652-86,945,816 , GRCh38.p12 chr7: 87,311,336-87,316,500	0
nsv3318894	copy number variation	19	nstd157	human		GRCh37 chr12: 6,242,892-6,247,923 , GRCh38.p12 chr12: 6,133,726-6,138,757	0
nsv3318364	copy number variation	5	nstd157	human		GRCh38.p12 chr2: 18,145,582-18,161,979 , GRCh37 chr2: 18,326,848-18,343,245	0
nsv3318506	copy number variation	4	nstd157	human		GRCh38.p12 chr1: 58,256,134-58,268,081 , GRCh37 chr1: 58,721,806-58,733,753	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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