M2212 AND nstd157 - dbVar - NCBI

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Items: 15

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Number of Variants: 15

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
nsv3317759	copy number variation	12	nstd157	human		GRCh37 chr2: 66,188,209-66,196,726 , GRCh38.p12 chr2: 65,961,075-65,969,592	LINC02934
nsv3318346	copy number variation	1	nstd157	human		GRCh37 chr2: 114,158,840-114,165,681 , GRCh38.p12 chr2: 113,401,263-113,408,104	LINC02966
nsv3318911	copy number variation	2	nstd157	human		GRCh38.p12 chr19: 52,821,945-52,855,636 , GRCh37 chr19: 53,325,198-53,358,889	ZNF28, ZNF468
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
nsv3317352	copy number variation	5	nstd157	human		GRCh38.p12 chr1: 12,848,738-12,860,073 , GRCh37 chr1: 12,908,591-12,919,928 , GRCh38.p12 chr1\|NW_012132914.1: 30,251-41,586	PRAMEF2, HNRNPCL1
nsv3318174	copy number variation	14	nstd157	human		GRCh37 chr3: 186,408,475-186,418,850 , GRCh38.p12 chr3: 186,690,686-186,701,061	HRGP1, HRG-AS1
nsv3317916	copy number variation	17	nstd157	human		GRCh38.p12 chr15: 25,179,434-25,185,507 , GRCh37 chr15: 25,424,581-25,430,654	SNORD115-6, SNORD115-7, 3 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
nsv3318202	copy number variation	7	nstd157	human		GRCh37 chr4: 156,959,568-156,973,205 , GRCh38.p12 chr4: 156,038,416-156,052,053	0
nsv3318498	copy number variation	17	nstd157	human		GRCh37 chr4: 108,064,023-108,076,102 , GRCh38.p12 chr4: 107,142,866-107,154,945	0
nsv3317503	copy number variation	1	nstd157	human		GRCh37 chr8: 15,778,007-15,787,304 , GRCh38.p12 chr8: 15,920,498-15,929,795	0
nsv3318156	copy number variation	7	nstd157	human		GRCh37 chr11: 85,890,037-85,895,915 , GRCh38.p12 chr11: 86,178,995-86,184,873	0
nsv3318979	copy number variation	1	nstd157	human		GRCh37 chr18: 28,132,577-28,213,079 , GRCh38.p12 chr18: 30,552,611-30,633,113	0
nsv3318472	copy number variation	2	nstd157	human		GRCh38.p12 chr16: 32,531,415-32,590,988 , GRCh37 chr16: 32,542,736-32,602,309	0

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