NA18532 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
nsv438141	copy number variation	2	nstd20	human		NCBI34 chrX: 83,958,997-83,971,986 , GRCh37.p13 chrX: 85,187,140-85,200,129 , GRCh38.p12 chrX: 85,932,135-85,945,124	CHM
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
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
nsv438142	copy number variation	2	nstd20	human		NCBI34 chrX: 84,097,369-84,104,170 , GRCh37.p13 chrX: 85,325,512-85,332,313 , GRCh38.p12 chrX: 86,070,508-86,077,309	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
nsv437931	copy number variation	36	nstd20	human		NCBI34 chr4: 115,637,062-115,641,110 , GRCh37.p13 chr4: 115,178,242-115,182,290 , GRCh38.p12 chr4: 114,257,086-114,261,134	0
nsv438113	copy number variation	6	nstd20	human		NCBI34 chr9: 124,896,840-124,898,353 , GRCh37.p13 chr9: 129,520,795-129,522,308 , GRCh38.p12 chr9: 126,758,516-126,760,029	0

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