NA18943 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
nsv438153	copy number variation	2	nstd20	human		NCBI34 chrX: 114,373,214-114,373,881 , GRCh37.p13 chrX\|NW_004070892.1: 618,997-619,664 , GRCh37.p13 chrX: 115,589,112-115,589,779 , GRCh38.p12 chrX: 116,457,946-116,458,613	SLC6A14
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
nsv438338	copy number variation	81	nstd20	human		NCBI34 chr22: 21,026,944-21,558,650 , GRCh37.p13 chr22: 22,702,390-23,234,096 , GRCh38.p12 chr22: 22,348,040-22,891,916	BCRP4, IGL, 72 more genes
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
nsv438396	copy number variation	4	nstd20	human		NCBI34 chr3: 35,977,058-36,016,014 , GRCh37.p13 chr3: 36,016,433-36,055,389 , GRCh38.p12 chr3: 35,974,941-36,013,897	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
nsv437945	copy number variation	16	nstd20	human		NCBI34 chr4: 162,456,693-162,462,242 , GRCh37.p13 chr4: 161,879,066-161,884,615 , GRCh38.p12 chr4: 160,957,914-160,963,463	0
nsv438005	copy number variation	72	nstd20	human		NCBI34 chr7: 125,601,054-125,603,762 , GRCh37.p13 chr7: 126,046,565-126,049,273 , GRCh38.p12 chr7: 126,406,511-126,409,219	0

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