NA18949 AND nstd20 - dbVar - NCBI

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Number of Variants: 10

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
nsv437902	copy number variation	9	nstd20	human		NCBI34 chr3: 190,685,007-190,688,562 , GRCh37.p13 chr3: 189,364,094-189,367,649 , GRCh38.p12 chr3: 189,646,305-189,649,860	TP63
nsv438035	copy number variation	6	nstd20	human		NCBI34 chr8: 9,537,015-9,537,654 , GRCh37.p13 chr8: 9,499,605-9,500,244 , GRCh38.p12 chr8: 9,642,095-9,642,734 , GRCh38.p12 chr8\|NW_018654717.1: 3,708,766-3,709,405	TNKS
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
nsv438337	copy number variation	50	nstd20	human		NCBI34 chr2: 52,726,065-52,757,084 , GRCh37.p13 chr2: 52,751,531-52,782,550 , GRCh38.p12 chr2: 52,524,393-52,555,412	0
nsv437916	copy number variation	2	nstd20	human		NCBI34 chr4: 32,163,126-32,169,581 , GRCh37.p13 chr4: 32,298,443-32,304,898 , GRCh38.p12 chr4: 32,296,821-32,303,276	0
nsv437919	copy number variation	22	nstd20	human		NCBI34 chr4: 63,672,955-63,678,558 , GRCh37.p13 chr4: 63,669,575-63,675,178 , GRCh38.p12 chr4: 62,803,857-62,809,460	0
nsv437880	copy number variation	7	nstd20	human		NCBI34 chr3: 131,109,842-131,114,005 , GRCh37.p13 chr3: 129,788,933-129,793,096 , GRCh38.p12 chr3: 130,070,090-130,074,253	0
nsv437868	copy number variation	41	nstd20	human		NCBI34 chr3: 99,731,950-99,732,552 , GRCh37.p13 chr3: 98,411,049-98,411,651 , GRCh38.p12 chr3: 98,692,205-98,692,807	0

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