M2269 AND nstd157 - dbVar - NCBI

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Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3318970	copy number variation	1	nstd157	human		GRCh37 chr16: 81,262,147-81,278,138 , GRCh38.p12 chr16: 81,228,542-81,244,533	BCO1
nsv3317594	copy number variation	18	nstd157	human		GRCh37 chr1: 245,636,915-245,647,809 , GRCh38.p12 chr1: 245,473,613-245,484,507 , GRCh38.p12 chr1\|NT_187516.1: 167,917-178,811	KIF26B
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
nsv3317836	copy number variation	19	nstd157	human		GRCh37 chr18: 67,208,806-67,217,271 , GRCh38.p12 chr18: 69,541,570-69,550,035	DOK6
nsv3318891	copy number variation	13	nstd157	human		GRCh37 chr9: 139,668,443-139,676,734 , GRCh38.p12 chr9: 136,773,991-136,782,282	ATP6V1G1P3
nsv3317167	copy number variation	1	nstd157	human		GRCh38.p12 chr8: 13,902,910-14,054,408 , GRCh37 chr8: 13,760,419-13,911,917	LOC100421160, LOC100421673
nsv3317296	copy number variation	1	nstd157	human		GRCh38.p12 chr6: 32,541,802-32,581,757 , GRCh37 chr6: 32,509,579-32,549,534	HLA-DRB1, HLA-DRB6, 2 more genes
nsv3317200	copy number variation	7	nstd157	human		GRCh37 chr17: 44,166,604-44,288,620 , GRCh38.p12 chr17: 46,089,238-46,211,254 , GRCh38.p12 chr17\|NT_187663.1: 791,339-913,427	KANSL1, KANSL1-AS1, 1 more genes
nsv3318758	copy number variation	1	nstd157	human		GRCh37 chr7: 111,943,602-112,016,581 , GRCh38.p12 chr7: 112,303,547-112,376,526	ZNF277, MTND5P8, 3 more genes
nsv3317327	copy number variation	24	nstd157	human		GRCh38.p12 chr2: 241,911,938-242,092,368 , GRCh37 chr2: 242,854,089-243,034,519 , GRCh38.p12 chr2\|NT_187647.1: 1-136,078 , GRCh38.p12 chr2\|NT_187523.1: 1-136,438	LOC285097, LINC01881, 4 more genes
nsv3317146	copy number variation	3	nstd157	human		GRCh37 chr3: 62,961,431-62,993,936 , GRCh38.p12 chr3: 62,975,756-63,008,260	0
nsv3318533	copy number variation	1	nstd157	human		GRCh37 chr8: 13,712,661-13,737,515 , GRCh38.p12 chr8: 13,855,152-13,880,006	0
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
nsv3317162	copy number variation	5	nstd157	human		GRCh37 chr6: 77,315,788-77,326,802 , GRCh38.p12 chr6: 76,606,071-76,617,085	0
nsv3318432	copy number variation	41	nstd157	human		GRCh37 chr8: 5,595,511-5,605,706 , GRCh38.p12 chr8: 5,737,989-5,748,184	0
nsv3318041	copy number variation	1	nstd157	human		GRCh37 chr17: 75,641,916-75,650,825 , GRCh38.p12 chr17: 77,645,834-77,654,743	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
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
nsv3317249	copy number variation	11	nstd157	human		GRCh38.p12 chr6: 68,521,991-68,532,062 , GRCh37 chr6: 69,231,883-69,241,954	0

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