NA19208 AND nstd20 - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
nsv437917	copy number variation	23	nstd20	human	NCBI34 chr4: 34,677,422-34,762,467 , GRCh37.p13 chr4\|NW_003315915.1: 270,949-355,994 , GRCh37.p13 chr4: 34,780,242-34,865,287 , GRCh38.p12 chr4: 34,778,620-34,863,665 , GRCh38.p12 chr4\|NW_003315915.1: 270,949-355,994	LOC105378262
nsv438048	copy number variation	78	nstd20	human	NCBI34 chr1: 149,771,758-149,800,260 , GRCh37.p13 chr1: 152,555,176-152,583,678 , GRCh38.p12 chr1: 152,582,700-152,611,202	LCE3C
nsv437859	copy number variation	8	nstd20	human	NCBI34 chr1: 55,871-68,941 , GRCh37.p13 chr1: 66,008-79,078 , GRCh38.p12 chr1: 66,008-79,078	OR4F5
nsv438379	copy number variation	14	nstd20	human	NCBI34 chr2: 203,499,611-203,511,609 , GRCh37.p13 chr2: 203,297,068-203,309,066 , GRCh38.p12 chr2: 202,432,345-202,444,343	BMPR2
nsv438355	copy number variation	4	nstd20	human	NCBI34 chr1: 16,634,909-16,646,447 , GRCh37.p13 chr1: 17,253,828-17,265,366 , GRCh38.p12 chr1: 16,927,333-16,938,871	CROCC
nsv437889	copy number variation	12	nstd20	human	NCBI34 chr3: 156,501,087-156,505,963 , GRCh37.p13 chr3: 155,180,174-155,185,050 , GRCh38.p12 chr3: 155,462,385-155,467,261	PLCH1
nsv438050	copy number variation	126	nstd20	human	GRCh38.p12 chr8: 39,375,220-39,536,536 , NCBI34 chr8: 39,250,107-39,411,423 , GRCh37.p13 chr8: 39,232,739-39,394,055	ADAM3A, ADAM5
nsv438097	copy number variation	7	nstd20	human	NCBI34 chr9: 21,275,389-21,296,318 , GRCh38.p12 chr9: 21,285,390-21,306,319 , GRCh37.p13 chr9: 21,285,389-21,306,318	IFNA5, LOC107987053
nsv437922	copy number variation	25	nstd20	human	GRCh38.p12 chr4: 69,231,212-69,361,702 , GRCh37.p13 chr4: 70,096,930-70,227,420 , NCBI34 chr4: 70,412,475-70,542,965	UGT2B28, LOC642496, 2 more genes
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
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
nsv438205	copy number variation	7	nstd20	human	NCBI34 chr12: 36,397,599-36,433,840 , GRCh37.p13 chr12: 38,111,332-38,147,573 , GRCh38.p12 chr12: 37,717,530-37,753,771	0
nsv437932	copy number variation	4	nstd20	human	NCBI34 chr4: 116,620,794-116,631,153 , GRCh37.p13 chr4: 116,161,974-116,172,333 , GRCh38.p12 chr4: 115,240,818-115,251,177	0
nsv438191	copy number variation	6	nstd20	human	NCBI34 chr12: 12,031,052-12,037,271 , GRCh37.p13 chr12: 12,139,785-12,146,004 , GRCh38.p12 chr12: 11,986,851-11,993,070	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
nsv438178	copy number variation	3	nstd20	human	NCBI34 chr10: 66,655,021-66,658,072 , GRCh37.p13 chr10: 67,310,418-67,313,469 , GRCh38.p12 chr10: 65,550,660-65,553,711 , GRCh38.p12 chr10\|NW_013171806.1: 51,253-54,304	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
nsv437975	copy number variation	4	nstd20	human	NCBI34 chr6: 93,571,379-93,573,957 , GRCh37.p13 chr6: 93,575,781-93,578,359 , GRCh38.p12 chr6: 92,866,063-92,868,641	0
nsv438295	copy number variation	2	nstd20	human	NCBI34 chr18: 61,878,056-61,879,919 , GRCh37.p13 chr18: 63,729,087-63,730,950 , GRCh38.p12 chr18: 66,061,851-66,063,714	0
nsv438082	copy number variation	4	nstd20	human	NCBI34 chr1: 155,737,529-155,738,184 , GRCh37.p13 chr1: 158,520,737-158,521,392 , GRCh38.p12 chr1: 158,550,947-158,551,602	0

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Number of Variants: 20

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