NA18633 AND nstd20 - dbVar - NCBI

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Items: 9

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Number of Variants: 9

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
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
nsv437903	copy number variation	23	nstd20	human		NCBI34 chr3: 191,058,267-191,060,542 , GRCh37.p13 chr3: 189,737,354-189,739,629 , GRCh38.p12 chr3: 190,019,565-190,021,840	P3H2
nsv437884	copy number variation	3	nstd20	human		NCBI34 chr3: 133,312,348-133,312,893 , GRCh37.p13 chr3: 131,991,439-131,991,984 , GRCh38.p12 chr3: 132,272,595-132,273,140	CPNE4
nsv438008	copy number variation	228	nstd20	human		NCBI34 chr7: 141,456,537-141,472,512 , GRCh38.p12 chr7\|NT_187562.1: 311,217-327,170 , GRCh37.p13 chr7\|NW_003571040.1: 491,288-507,241	TRB, TRBV6-2, 2 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
nsv438368	copy number variation	10	nstd20	human		NCBI34 chr2: 123,575,969-123,577,446 , GRCh37.p13 chr2: 123,480,824-123,482,301 , GRCh38.p12 chr2: 122,723,248-122,724,725	0
nsv438152	copy number variation	2	nstd20	human		NCBI34 chrX: 110,928,593-110,929,387 , GRCh37.p13 chrX: 112,164,622-112,165,416 , GRCh38.p12 chrX: 112,921,394-112,922,188	0

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