1-0638-002 AND nstd173 - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
nsv4380489	copy number variation	13	nstd173	human	GRCh37 chr1: 196,716,413-196,741,354 , GRCh38.p12 chr1: 196,747,283-196,772,224	CFH
nsv4372918	copy number variation	35	nstd173	human	GRCh37 chr11: 18,941,197-18,961,268 , GRCh38.p12 chr11: 18,919,650-18,939,721	MRGPRX1
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
nsv4376456	copy number variation	1782	nstd173	human	GRCh37 chr8: 39,246,772-39,386,964 , GRCh38.p12 chr8: 39,389,253-39,529,445	ADAM5, ADAM3A
nsv4382153	copy number variation	3	nstd173	human	GRCh37 chr1: 1,397,630-1,429,163 , GRCh38.p12 chr1: 1,462,250-1,493,783	ATAD3B, ATAD3C
nsv4376418	copy number variation	25	nstd173	human	GRCh37 chr12: 2,235,941-2,258,023 , GRCh38.p12 chr12: 2,126,775-2,148,857 , GRCh38.p12 chr12\|NW_018654718.1: 468,919-491,001	LOC107984131, CACNA1C
nsv4381433	copy number variation	68	nstd173	human	GRCh37 chr1: 196,827,842-196,877,049 , GRCh38.p12 chr1: 196,858,712-196,907,919	LOC100996886, CFHR4
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
nsv4370364	copy number variation	28	nstd173	human	GRCh37 chr4: 69,367,093-69,485,978 , GRCh38.p12 chr4: 68,501,375-68,620,260	LOC100422402, UGT2B17, 2 more genes
nsv4383294	copy number variation	35	nstd173	human	GRCh37 chr11: 55,376,498-55,442,305 , GRCh38.p12 chr11: 55,609,022-55,674,829	OR4V1P, OR4S2, 2 more genes
nsv4370277	copy number variation	687	nstd173	human	GRCh37 chr5: 180,378,754-180,430,789 , GRCh38.p12 chr5: 180,951,754-181,003,789	BTNL8, ARPP19P1, 3 more genes
nsv4374986	copy number variation	22	nstd173	human	GRCh37 chr14: 74,001,111-74,029,903 , GRCh38.p12 chr14: 73,534,407-73,563,199	NT5CP2, HEATR4, 1 more genes
nsv4372664	copy number variation	11	nstd173	human	GRCh37 chr14: 107,150,444-107,173,910 , GRCh38.p12 chr14: 106,694,427-106,718,663	IGH, IGHV1-69, 2 more genes
nsv4370006	copy number variation	1	nstd173	human	GRCh37 chr7: 64,576,418-65,091,623 , GRCh38.p12 chr7: 65,116,040-65,626,710	ZNF92, RSL24D1P3, 8 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
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
nsv4374525	copy number variation	13	nstd173	human	GRCh37 chr7: 38,319,296-38,352,147 , GRCh38.p12 chr7: 38,279,695-38,312,546	TRG, TRGV11, 4 more genes
nsv4371643	copy number variation	1	nstd173	human	GRCh37 chr8: 6,999,114-8,147,599 , GRCh38.p12 chr8: 7,141,592-8,290,077	DEFB108A, SNRPCP6, 81 more genes
nsv4386339	copy number variation	89	nstd173	human	GRCh37 chr16: 34,466,475-34,755,828 , GRCh38.p12 chr16: 35,232,104-35,521,457	LOC105371204, C2orf69P4, 26 more genes
nsv4385737	copy number variation	3	nstd173	human	GRCh37 chr14: 22,676,929-22,959,555 , GRCh38.p12 chr14: 22,209,033-22,490,567	TRAJ50, TRDD2, 36 more genes

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