NA18582 AND nstd20 - dbVar - NCBI

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Number of Variants: 8

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv438301	copy number variation	1	nstd20	human		NCBI34 chr18: 74,909,007-74,923,022 , GRCh37.p13 chr18\|NW_003315961.1: 120,580-134,595 , GRCh37.p13 chr18: 76,810,030-76,824,045 , GRCh38.p12 chr18: 79,050,030-79,064,045 , GRCh38.p12 chr18\|NT_187666.1: 118,743-132,758 , GRCh38.p12 chr18\|NW_003315961.1: 120,580-134,595	LOC105372225
nsv437907	copy number variation	146	nstd20	human		NCBI34 chr3: 194,196,286-194,205,086 , GRCh37.p13 chr3: 192,875,373-192,884,173 , GRCh38.p12 chr3: 193,157,584-193,166,384	VEZF1P1
nsv438011	copy number variation	95	nstd20	human		NCBI34 chr7: 141,921,685-141,931,471 , GRCh37.p13 chr7: 142,481,301-142,486,383 , GRCh38.p12 chr7\|NT_187562.1: 776,047-785,840 , GRCh37.p13 chr7\|NW_003571040.1: 956,118-965,911	TRB, PRSS3P2, 1 more genes
nsv437921	copy number variation	122	nstd20	human		GRCh37.p13 chr: NaN-NaN , GRCh38.p12 chr: NaN-NaN , NCBI34 chr4: 69,377,786-69,808,237	0
nsv437894	copy number variation	301	nstd20	human		NCBI34 chr3: 163,826,348-163,943,569 , GRCh37.p13 chr3: 162,505,435-162,622,656 , GRCh38.p12 chr3: 162,787,647-162,904,868	0
nsv438371	copy number variation	55	nstd20	human		NCBI34 chr2: 147,075,728-147,086,685 , GRCh37.p13 chr2: 146,864,959-146,875,916 , GRCh38.p12 chr2: 146,107,391-146,118,348	0
nsv438390	copy number variation	3	nstd20	human		NCBI34 chr3: 15,366,898-15,373,051 , GRCh37.p13 chr3: 15,391,894-15,398,047 , GRCh38.p12 chr3: 15,350,387-15,356,540	0
nsv438113	copy number variation	6	nstd20	human		NCBI34 chr9: 124,896,840-124,898,353 , GRCh37.p13 chr9: 129,520,795-129,522,308 , GRCh38.p12 chr9: 126,758,516-126,760,029	0

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