CONTROL_28 AND nstd53 - dbVar - NCBI

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Items: 11

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Number of Variants: 11

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv870318	copy number variation	1	nstd53	human		GRCh37.p13 chr3: 162,494,699-162,819,441 , GRCh38.p12 chr3: 162,776,911-163,101,653 , NCBI36 chr3: 163,977,393-164,302,135	RPS6P4
nsv870073	copy number variation	19	nstd53	human		GRCh38.p12 chr6: 303,298-347,329 , NCBI36 chr6: 248,298-292,329 , GRCh37.p13 chr6: 303,298-347,329	DUSP22
nsv869857	copy number variation	1	nstd53	human		GRCh38.p12 chr4: 114,842,382-114,879,890 , GRCh37.p13 chr4: 115,763,538-115,801,046 , NCBI36 chr4: 115,982,987-116,020,495	NDST4
nsv869807	copy number variation	87	nstd53	human		NCBI36 chr11: 55,118,273-55,200,744 , GRCh37.p13 chr11: 55,361,697-55,444,168 , GRCh38.p12 chr11: 55,594,221-55,676,692	OR4V1P, OR4P4, 3 more genes
nsv869657	copy number variation	12	nstd53	human		NCBI36 chr1: 25,482,095-25,541,997 , GRCh38.p12 chr1: 25,283,017-25,342,919 , GRCh37.p13 chr1: 25,609,508-25,669,410	RHD, TMEM50A, 2 more genes
nsv869574	copy number variation	8	nstd53	human		GRCh38.p12 chr10: 133,475,375-133,558,930 , NCBI36 chr10: 135,138,869-135,222,424 , GRCh37.p13 chr10: 135,288,879-135,372,434	CYP2E1, OR7M1P, 3 more genes
nsv869910	copy number variation	14	nstd53	human		GRCh38.p12 chr2: 241,914,496-242,092,126 , NCBI36 chr2: 242,505,320-242,682,950 , GRCh37.p13 chr2: 242,856,647-243,034,277 , GRCh38.p12 chr2\|NT_187647.1: 1-135,836 , GRCh38.p12 chr2\|NT_187523.1: 1-136,196	LOC285097, LINC01881, 4 more genes
nsv869577	copy number variation	64	nstd53	human		NCBI36 chr15: 18,867,344-19,943,194 , GRCh38.p12 chr15: 20,402,077-22,153,879 , GRCh37.p13 chr15: 20,607,330-22,441,830	NBEAP1, OR4H6P, 78 more genes
nsv869711	copy number variation	90	nstd53	human		NCBI36 chr4: 69,099,876-69,643,272 , GRCh37.p13 chr: NaN-NaN , GRCh38.p12 chr: NaN-NaN	0
nsv870238	copy number variation	6	nstd53	human		GRCh38.p12 chr10: 45,674,428-47,923,579 , NCBI36 chr10: 45,489,882-47,946,216 , GRCh37.p13 chr10: 46,169,876-48,055,707 , GRCh37.p13 chr10\|NW_003871068.1: 1-2,010,264	CTSLP2, GDF2, 71 more genes
nsv869782	copy number variation	92	nstd53	human		NCBI36 chr14: 19,273,348-19,478,367 , GRCh38.p12 chr14: 19,735,349-19,940,368 , GRCh37.p13 chr14: 20,203,508-20,408,527	OR4K6P, OR4K5, 10 more genes

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CONTROL_28 AND nstd53 (12)
dbVar
C1853995[trait identifier] AND "Fulgent Genetics, Fulgent Genetic... (8)
C1853995[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[submitter]
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