NA18550 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
nsv438014	copy number variation	27	nstd20	human		NCBI34 chr8: 534,755-588,391 , GRCh37.p13 chr8: 544,755-598,391 , GRCh38.p12 chr8: 594,755-648,391	ERICH1
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
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
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
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
nsv438314	copy number variation	1	nstd20	human		NCBI34 chr21: 13,588,035-13,603,210 , GRCh37.p13 chr21: 14,666,164-14,681,339 , GRCh38.p12 chr21: 13,293,843-13,309,018	0
nsv438313	copy number variation	1	nstd20	human		NCBI34 chr21: 13,483,810-13,497,625 , GRCh37.p13 chr21: 14,561,939-14,575,754 , GRCh38.p12 chr21: 13,189,618-13,203,433	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

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