NA18956 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
nsv437997	copy number variation	8	nstd20	human		NCBI34 chr7: 109,735,375-109,745,762 , GRCh37.p13 chr7: 110,174,844-110,185,231 , GRCh38.p12 chr7: 110,534,787-110,545,174	LOC105375451
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
nsv438078	copy number variation	6	nstd20	human		NCBI34 chr8: 115,540,689-115,611,467 , GRCh37.p13 chr8: 115,584,106-115,654,884 , GRCh38.p12 chr8: 114,571,877-114,642,655	0
nsv437910	copy number variation	98	nstd20	human		NCBI34 chr4: 9,969,524-9,998,131 , GRCh37.p13 chr4: 10,218,641-10,247,248 , GRCh38.p12 chr4: 10,217,017-10,245,624	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
nsv438043	copy number variation	32	nstd20	human		NCBI34 chr8: 16,211,924-16,216,726 , GRCh37.p13 chr8: 16,201,558-16,206,360 , GRCh38.p12 chr8: 16,344,049-16,348,851	0

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