1-1013-003 AND nstd173 - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
nsv4378257	copy number variation	2	nstd173	human	GRCh37 chr2: 15,158,840-15,198,697 , GRCh38.p12 chr2: 15,018,716-15,058,573	NBAS
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
nsv4367048	copy number variation	1	nstd173	human	GRCh37 chr9: 7,306,425-7,327,084 , GRCh38.p12 chr9: 7,306,425-7,327,084	LOC105375970
nsv4373449	copy number variation	132	nstd173	human	GRCh37 chr2: 98,138,417-98,162,176 , GRCh38.p12 chr2: 97,521,954-97,545,713	ANKRD36B
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
nsv4375212	copy number variation	547	nstd173	human	GRCh37 chr1: 72,762,663-72,811,904 , GRCh38.p12 chr1: 72,296,980-72,346,221 , GRCh38.p12 chr1\|NW_018654707.1: 9,247-67,446	RPL31P12, LOC105378797
nsv4365971	copy number variation	432	nstd173	human	GRCh37 chr1: 248,753,196-248,795,289 , GRCh38.p12 chr1: 248,589,895-248,631,988	OR2T10, OR2T11
nsv4369152	copy number variation	2	nstd173	human	GRCh37 chr19: 41,352,626-41,380,933 , GRCh38.p12 chr19: 40,846,721-40,875,028	CYP2A6, CYP2A7
nsv4384822	copy number variation	80	nstd173	human	GRCh37 chr7: 43,361-81,400 , GRCh38.p12 chr7: 43,361-81,400 , GRCh38.p12 chr7\|NT_187558.1: 1-37,499 , GRCh38.p12 chr7\|NT_187653.1: 35,682-73,721	LOC105375113, LOC101929756
nsv4376755	copy number variation	329	nstd173	human	GRCh37 chr14: 74,001,122-74,024,031 , GRCh38.p12 chr14: 73,534,418-73,557,327	ACOT1, NT5CP2, 1 more genes
nsv4379867	copy number variation	5	nstd173	human	GRCh37 chr12: 11,220,827-11,241,337 , GRCh38.p12 chr12: 11,068,228-11,088,738	TAS2R64P, PRH1-TAS2R14, 2 more genes
nsv4381169	copy number variation	1	nstd173	human	GRCh37 chr10: 47,084,852-48,174,779 , GRCh38.p12 chr10: 46,157,935-47,923,579	LOC102724593, GPRIN2, 54 more genes
nsv4368660	copy number variation	868	nstd173	human	GRCh37 chr6: 103,738,197-103,759,824 , GRCh38.p12 chr6: 103,290,322-103,311,949	0
nsv4386306	copy number variation	141	nstd173	human	GRCh37 chrX: 924,088-944,608 , GRCh38.p12 chrX: 963,353-983,873	0
nsv4375393	copy number variation	59	nstd173	human	GRCh37 chr17: 36,283,807-36,410,559 , GRCh38.p12 chr17\|NT_187614.1: 2,162,872-2,289,624	NPEPPSP1, TBC1D3, 6 more genes
nsv4377250	copy number variation	1	nstd173	human	GRCh37 chr2: 130,817,326-131,184,830 , GRCh38.p12 chr2: 130,059,753-130,427,257	IMP4, SMPD4, 30 more genes
nsv4385961	copy number variation	2	nstd173	human	GRCh37 chr14: 22,772,289-22,960,757 , GRCh38.p12 chr14: 22,304,404-22,491,770	TRAJ49, TRAJ61, 32 more genes
nsv4372860	copy number variation	1	nstd173	human	GRCh37 chr6: 58,071,364-58,223,181 , GRCh38.p12 chr: NaN-NaN	0
nsv4372589	copy number variation	741	nstd173	human	GRCh37 chr14: 106,530,472-106,560,975 , GRCh38.p12 chr: NaN-NaN	0
nsv4387382	copy number variation	84	nstd173	human	GRCh37 chr5: 57,326,026-57,349,970 , GRCh38.p12 chr5: 58,030,199-58,054,143	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