OCD52-S_0625-8219-1 AND nstd173 - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
nsv4368493	copy number variation	1	nstd173	human	GRCh37 chr4: 116,399,074-116,581,649 , GRCh38.p12 chr4: 115,477,918-115,660,493	RPF2P2
nsv4379349	copy number variation	357	nstd173	human	GRCh37 chr20: 1,560,549-1,597,997 , GRCh38.p12 chr20: 1,579,903-1,617,351	SIRPB1
nsv4384081	copy number variation	8	nstd173	human	GRCh37 chr5: 2,037,608-2,062,048 , GRCh38.p12 chr5: 2,037,494-2,061,934
nsv4381915	copy number variation	18	nstd173	human	GRCh37 chr8: 39,246,772-39,386,952 , GRCh38.p12 chr8: 39,389,253-39,529,433	ADAM3A, ADAM5
nsv4388544	copy number variation	68	nstd173	human	GRCh37 chrX: 62,470,734-62,505,606 , GRCh38.p12 chrX: 63,250,857-63,285,729	LOC105377212, LOC100533730
nsv4383876	copy number variation	9	nstd173	human	GRCh37 chr17: 44,212,310-44,292,754 , GRCh38.p12 chr17: 46,134,944-46,215,388 , GRCh38.p12 chr17\|NT_187663.1: 837,051-917,561	LOC107985027, KANSL1, 1 more genes
nsv4384457	copy number variation	635	nstd173	human	GRCh37 chr11: 55,374,031-55,453,008 , GRCh38.p12 chr11: 55,606,555-55,685,532	OR4P1P, OR4C6, 3 more genes
nsv4383038	copy number variation	15	nstd173	human	GRCh37 chr5: 180,374,898-180,430,801 , GRCh38.p12 chr5: 180,947,898-181,003,801	BTNL8, ARPP19P1, 3 more genes
nsv4370631	copy number variation	136	nstd173	human	GRCh37 chr11: 5,787,573-5,809,230 , GRCh38.p12 chr11: 5,766,343-5,788,000	OR52N1, OR56B2P, 1 more genes
nsv4373048	copy number variation	1	nstd173	human	GRCh37 chr16: 948,966-1,003,554 , GRCh38.p12 chr16: 898,966-953,554	LMF1, LOC107984876, 1 more genes
nsv4366223	copy number variation	4	nstd173	human	GRCh37 chr19: 55,247,894-55,298,567 , GRCh38.p12 chr19\|NT_187693.1: 719,008-769,681	KIR2DL1, KIR2DL3, 4 more genes
nsv4381531	copy number variation	237	nstd173	human	GRCh37 chr2: 34,701,643-34,737,163 , GRCh38.p12 chr2: 34,476,576-34,512,096	0
nsv4380431	copy number variation	2	nstd173	human	GRCh37 chr4: 165,569,118-165,598,638 , GRCh38.p12 chr4: 164,647,966-164,677,486	0
nsv4382392	copy number variation	421	nstd173	human	GRCh37 chr3: 65,185,849-65,210,375 , GRCh38.p12 chr3: 65,200,174-65,224,700	0
nsv4369404	copy number variation	213	nstd173	human	GRCh37 chr14: 107,150,444-107,179,594 , GRCh38.p12 chr14: 106,694,427-106,771,352	IGHV2-70, IGH, 7 more genes
nsv4365115	copy number variation	3	nstd173	human	GRCh37 chr19: 54,722,672-54,752,217 , GRCh38.p12 chr19: 54,218,803-54,248,358 , GRCh38.p12 chr19\|NT_187693.1: 193,786-223,331 , GRCh38.p12 chr19\|NW_003571061.2: 193,786-223,362 , GRCh38.p12 chr19\|NW_003571060.1: 193,789-223,326 , GRCh38.p12 chr19\|NW_003571054.1: 193,603-223,093	LOC102725035, LOC107987462, 7 more genes
nsv4381227	copy number variation	3	nstd173	human	GRCh37 chr14: 22,533,752-22,971,360 , GRCh38.p12 chr14: 22,065,488-22,502,376	TRAV41, TRDJ3, 63 more genes
nsv4377247	copy number variation	17	nstd173	human	GRCh37 chr7: 142,266,307-142,486,548 , GRCh38.p12 chr7: 142,618,685-142,778,738 , GRCh38.p12 chr7\|NT_187562.1: 656,734-781,128	PRSS2, MTRNR2L6, 19 more genes
nsv4385533	copy number variation	9	nstd173	human	GRCh37 chr7: 38,295,932-38,391,352 , GRCh38.p12 chr7: 38,256,331-38,351,751	TRGV8, TRGV5P, 19 more genes
nsv4387573	copy number variation	172	nstd173	human	GRCh37 chr11: 54,701,632-54,757,928 , GRCh38.p12 chr11: 54,934,156-54,990,452	0

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Number of Variants: 20

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