M2388 AND nstd157 - dbVar - NCBI

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Items: 18

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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
nsv3317418	copy number variation	3	nstd157	human		GRCh37 chr15: 60,086,249-60,103,464 , GRCh38.p12 chr15: 59,794,050-59,811,265
nsv3317857	copy number variation	22	nstd157	human		GRCh37 chr15: 56,789,979-56,800,635 , GRCh38.p12 chr15: 56,497,781-56,508,437
nsv3318129	copy number variation	4	nstd157	human		GRCh37 chr10: 87,953,705-87,959,563 , GRCh38.p12 chr10: 86,193,948-86,199,806	GRID1
nsv3318752	copy number variation	1	nstd157	human		GRCh37 chr8: 57,254,332-57,286,801 , GRCh38.p12 chr8: 56,341,773-56,374,242	SDR16C6P
nsv3317671	copy number variation	1	nstd157	human		GRCh37 chr11: 93,903,779-93,908,872 , GRCh38.p12 chr11: 94,170,613-94,175,706	PANX1
nsv3318420	copy number variation	1	nstd157	human		GRCh38.p12 chr19: 49,568,440-49,588,745 , GRCh37 chr19: 50,071,697-50,092,002	PRRG2, NOSIP
nsv3318924	copy number variation	14	nstd157	human		GRCh38.p12 chr15: 97,271,952-97,288,602 , GRCh37 chr15: 97,815,182-97,831,832	LOC105371006, LINC02253
nsv3318040	copy number variation	1	nstd157	human		GRCh38.p12 chr2: 18,998,386-19,052,132 , GRCh37 chr2: 19,179,659-19,251,888	LINC01376,
nsv3317846	copy number variation	16	nstd157	human		GRCh38.p12 chr9: 133,071,778-133,082,065 , GRCh37 chr9: 135,947,165-135,957,452	CEL, CELP
nsv3317604	copy number variation	16	nstd157	human		GRCh38.p12 chr19: 54,225,207-54,238,862 , GRCh37 chr19: 54,729,079-54,742,738 , GRCh38.p12 chr19\|NW_003571060.1: 200,197-213,851 , GRCh38.p12 chr19\|NW_003571054.1: 200,007-213,635 , GRCh38.p12 chr19\|NT_187693.1: 200,193-213,852	LILRA6, LOC100421130, 1 more genes
nsv3317092	copy number variation	1	nstd157	human		GRCh38.p12 chr1: 236,506,166-236,649,097 , GRCh37 chr1: 236,669,466-236,812,397	LGALS8, HEATR1, 2 more genes
nsv3318259	copy number variation	1	nstd157	human		GRCh38.p12 chr19: 45,332,725-45,401,737 , GRCh37 chr19: 45,835,983-45,904,995	ERCC2, PPP1R13L, 2 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
nsv3317350	copy number variation	1	nstd157	human		GRCh37 chr7: 62,028,908-62,049,484 , GRCh38.p12 chr7: 62,568,530-62,589,106	0
nsv3317830	copy number variation	10	nstd157	human		GRCh37 chr5: 7,178,644-7,191,074 , GRCh38.p12 chr5: 7,178,531-7,190,961	0
nsv3318797	copy number variation	10	nstd157	human		GRCh37 chr5: 113,327,484-113,335,230 , GRCh38.p12 chr5: 113,991,787-113,999,533	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
nsv3317546	copy number variation	4	nstd157	human		GRCh37 chr3: 1,782,524-1,787,581 , GRCh38.p12 chr3: 1,740,840-1,745,897	0

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