14-0319-003 AND nstd173 - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
nsv4385455	copy number variation	190	nstd173	human	GRCh37 chr20: 1,557,177-1,597,997 , GRCh38.p12 chr20: 1,576,531-1,617,351	SIRPB1
nsv4370116	copy number variation	174	nstd173	human	GRCh37 chr2: 98,138,417-98,161,960 , GRCh38.p12 chr2: 97,521,954-97,545,497	ANKRD36B
nsv4371280	copy number variation	95	nstd173	human	GRCh37 chr1: 72,762,663-72,811,084 , GRCh38.p12 chr1: 72,296,980-72,345,401 , GRCh38.p12 chr1\|NW_018654707.1: 9,247-66,626	RPL31P12, LOC105378797
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
nsv4367271	copy number variation	561	nstd173	human	GRCh37 chr11: 5,786,020-5,809,230 , GRCh38.p12 chr11: 5,764,790-5,788,000	OR56B2P, OR52N1, 1 more genes
nsv4381865	copy number variation	16	nstd173	human	GRCh37 chr17: 34,440,853-34,477,480 , GRCh38.p12 chr17: 36,113,460-36,150,098 , GRCh38.p12 chr17\|NT_187661.1: 67,557-104,195 , GRCh38.p12 chr17\|NT_187614.1: 348,381-385,008	LOC101927369, LOC100419980, 2 more genes
nsv4368821	copy number variation	1373	nstd173	human	GRCh37 chr22: 24,353,749-24,385,040 , GRCh38.p12 chr22\|NT_187633.1: 247,924-279,215	LOC391322, GSTTP2, 3 more genes
nsv4370840	copy number variation	154	nstd173	human	GRCh37 chr12: 11,222,368-11,247,388 , GRCh38.p12 chr12: 11,069,769-11,094,789	TAS2R43, TAS2R64P, 3 more genes
nsv4371991	copy number variation	196	nstd173	human	GRCh37 chr19: 20,596,118-20,720,705 , GRCh38.p12 chr19: 20,413,312-20,537,899	ZNF826P, ZNF737, 4 more genes
nsv4369919	copy number variation	116	nstd173	human	GRCh37 chr14: 106,530,472-106,667,035 , GRCh38.p12 chr14: 106,074,229-106,210,392 , GRCh38.p12 chr14\|NT_187600.1: 541,998-678,161	IGHV1-18, IGHV3-20, 17 more genes
nsv4371199	copy number variation	115	nstd173	human	GRCh37 chr2: 52,738,983-52,790,493 , GRCh38.p12 chr2: 52,511,845-52,563,355	0
nsv4387023	copy number variation	344	nstd173	human	GRCh37 chr2: 34,701,643-34,727,784 , GRCh38.p12 chr2: 34,476,576-34,502,717	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
nsv4369274	copy number variation	262	nstd173	human	GRCh37 chr2: 35,976,209-35,997,473 , GRCh38.p12 chr2: 35,751,143-35,772,407	0
nsv4384501	copy number variation	242	nstd173	human	GRCh37 chr16: 19,945,795-19,965,942 , GRCh38.p12 chr16: 19,934,473-19,954,620	0
nsv4382973	copy number variation	317	nstd173	human	GRCh37 chr5: 180,378,754-180,442,428 , GRCh38.p12 chr5: 180,951,754-181,015,428	BTNL3, LOC100128762, 4 more genes
nsv4367173	copy number variation	1	nstd173	human	GRCh37 chr6: 27,699,004-27,758,520 , GRCh38.p12 chr6: 27,731,225-27,790,741	TRQ-CTG6-1, LOC100131289, 4 more genes
nsv4380168	copy number variation	295	nstd173	human	GRCh37 chr17: 44,187,492-44,784,639 , GRCh38.p12 chr17: 46,110,126-46,707,273 , GRCh38.p12 chr17\|NT_187663.1: 812,225-1,226,699	MAPK8IP1P1, DND1P2, 14 more genes
nsv4377337	copy number variation	1	nstd173	human	GRCh37 chr14: 22,761,289-22,960,619 , GRCh38.p12 chr14: 22,293,404-22,491,631	TRDJ4, TRAJ59, 32 more genes
nsv4386009	copy number variation	97	nstd173	human	GRCh37 chr5: 57,326,026-57,349,986 , GRCh38.p12 chr5: 58,030,199-58,054,159	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