SP50850 AND nstd71 - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
nsv901718	copy number variation	96	nstd71	human	NCBI36 chr14: 40,676,601-40,739,852 , GRCh37.p13 chr14: 41,606,851-41,670,102 , GRCh38.p12 chr14: 41,137,648-41,200,899	LINC02315
nsv884821	copy number variation	138	nstd71	human	NCBI36 chr6: 32,560,168-32,593,470 , GRCh37.p13 chr6: 32,452,190-32,485,492 , GRCh38.p12 chr6: 32,484,413-32,517,715	HLA-DRB5
nsv909839	copy number variation	966	nstd71	human	NCBI36 chr18: 64,895,268-64,909,808 , GRCh37.p13 chr18: 66,744,288-66,758,828 , GRCh38.p12 chr18: 69,077,051-69,091,591	CCDC102B
nsv885022	copy number variation	22	nstd71	human	NCBI36 chr6: 32,604,890-32,611,466 , GRCh37.p13 chr6: 32,496,912-32,503,488 , GRCh38.p12 chr6: 32,529,135-32,535,711	HLA-DRB5
nsv884980	copy number variation	2	nstd71	human	NCBI36 chr6: 32,593,489-32,606,019 , GRCh37.p13 chr6\|NT_167246.1: 3,995,584-4,010,110 , GRCh37.p13 chr6: 32,485,511-32,498,041 , GRCh37.p13 chr6\|NT_167245.1: 3,821,149-3,835,677 , GRCh38.p12 chr6: 32,517,734-32,530,264	HLA-DRB5
nsv903829	copy number variation	5	nstd71	human	NCBI36 chr15: 28,727,690-28,762,668 , GRCh37.p13 chr15: 30,940,398-30,975,376 , GRCh38.p12 chr15: 30,648,195-30,683,173 , GRCh38.p12 chr15\|NT_187660.1: 2,933,729-2,968,892 , GRCh38.p12 chr15\|NW_011332701.1: 2,821,277-2,856,440	ARHGAP11B, LOC100288637
nsv885201	copy number variation	6	nstd71	human	NCBI36 chr6: 32,616,207-32,626,983 , GRCh37.p13 chr6: 32,508,229-32,519,005 , GRCh38.p12 chr6: 32,540,452-32,551,228	RNU1-61P, HLA-DRB6
nsv879424	copy number variation	1	nstd71	human	NCBI36 chr4: 70,192,766-70,287,770 , GRCh37.p13 chr4: 70,158,177-70,253,181 , GRCh38.p12 chr4: 69,292,459-69,387,463	LOC100422190, LOC642496, 2 more genes
nsv879345	copy number variation	351	nstd71	human	NCBI36 chr4: 69,117,497-69,179,871 , GRCh37.p13 chr4: 69,434,902-69,497,276 , GRCh38.p12 chr4: 68,569,184-68,631,558	UGT2B17, LOC100132651, 2 more genes
nsv898108	copy number variation	7	nstd71	human	NCBI36 chr11: 89,232,539-89,260,302 , GRCh37.p13 chr11: 89,592,891-89,620,654 , GRCh38.p12 chr11: 89,859,723-89,887,486	TRIM51BP, TRIM64B, 1 more genes
nsv893145	copy number variation	2	nstd71	human	NCBI36 chr9: 40,708,561-40,814,035 , GRCh37.p13 chr9: 40,718,561-40,824,035 , GRCh38.p12 chr9: 66,868,806-66,974,280	FAM74A3, ZNF658, 1 more genes
nsv880751	copy number variation	7	nstd71	human	NCBI36 chr5: 786,926-887,280 , GRCh37.p13 chr5: 733,926-834,280 , GRCh38.p12 chr5: 733,811-834,165	ZDHHC11B, , 2 more genes
nsv911349	copy number variation	107	nstd71	human	NCBI36 chr19: 20,386,247-20,514,068 , GRCh37.p13 chr19\|NW_003571053.2: 329,860-456,675 , GRCh37.p13 chr19: 20,522,409-20,722,228 , GRCh38.p12 chr19: 20,411,600-20,539,422	ZNF826P, LOC105372316, 4 more genes
nsv883876	copy number variation	4	nstd71	human	NCBI36 chr6: 29,982,594-30,003,090 , GRCh37.p13 chr6\|NT_167246.1: 1,168,792-1,189,318 , GRCh37.p13 chr6: 29,874,615-29,895,111 , GRCh38.p12 chr6: 29,906,838-29,927,334 , GRCh38.p12 chr6\|NT_167246.2: 1,163,172-1,183,698	DDX39BP1, HCG4B, 4 more genes
nsv899666	copy number variation	72	nstd71	human	NCBI36 chr12: 130,362,098-130,395,261 , GRCh37.p13 chr12: 131,796,145-131,829,308 , GRCh38.p12 chr12: 131,311,600-131,344,763	0
nsv887000	copy number variation	53	nstd71	human	NCBI36 chr6: 169,246,516-169,267,945 , GRCh37.p13 chr6: 169,504,591-169,526,020 , GRCh38.p12 chr6: 169,104,496-169,125,925	0
nsv884258	copy number variation	146	nstd71	human	NCBI36 chr6: 31,388,306-31,398,785 , GRCh37.p13 chr6\|NT_167249.1: 2,614,037-2,624,528 , GRCh37.p13 chr6: 31,280,327-31,290,806 , GRCh38.p12 chr6: 31,312,550-31,323,029 , GRCh38.p12 chr6\|NT_167249.2: 2,614,739-2,625,230	0
nsv903856	copy number variation	1	nstd71	human	NCBI36 chr15: 29,806,023-30,255,140 , GRCh37.p13 chr15: 32,018,731-32,467,848 , GRCh38.p12 chr15: 31,726,528-32,175,647 , GRCh38.p12 chr15\|NT_187660.1: 4,011,664-4,440,034 , GRCh38.p12 chr15\|NW_011332701.1: 3,899,212-4,327,582	CHRNA7, DEPDC1P1, 3 more genes
nsv914626	copy number variation	19	nstd71	human	NCBI36 chr22: 22,668,071-22,734,578 , GRCh37.p13 chr22: 24,338,071-24,404,578 , GRCh38.p12 chr22\|NT_187633.1: 232,246-298,753	GSTT1-AS1, LOC391322, 6 more genes
nsv880294	copy number variation	63	nstd71	human	NCBI36 chr4: 162,075,534-162,151,909 , GRCh37.p13 chr4: 161,856,084-161,932,459 , GRCh38.p12 chr4: 160,934,932-161,011,307	0

dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Send to:

Search results

Items: 20

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Search details

Recent activity