2-1502-003 AND nstd173 - dbVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 17

loading data ...

Number of Variants: 17

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4379109	copy number variation	1337	nstd173	human		GRCh37 chr20: 1,560,774-1,597,997 , GRCh38.p12 chr20: 1,580,128-1,617,351	SIRPB1
nsv4387975	copy number variation	2	nstd173	human		GRCh37 chr7: 141,757,591-141,789,976 , GRCh38.p12 chr7: 142,057,791-142,090,176 , GRCh38.p12 chr7\|NT_187562.1: 19,671-52,056	MGAM
nsv4383158	copy number variation	25	nstd173	human		GRCh37 chr4: 44,965,183-45,006,191 , GRCh38.p12 chr4: 44,963,166-45,004,174	LOC100533736
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
nsv4372080	copy number variation	569	nstd173	human		GRCh37 chr1: 72,762,663-72,812,440 , GRCh38.p12 chr1: 72,296,980-72,346,757 , GRCh38.p12 chr1\|NW_018654707.1: 9,247-67,982	RPL31P12, LOC105378797
nsv4377390	copy number variation	1	nstd173	human		GRCh37 chr7: 56,612,148-56,648,111 , GRCh38.p12 chr7: 56,544,455-56,580,418	VN1R25P, LOC100130210
nsv4378165	copy number variation	86	nstd173	human		GRCh37 chr4: 69,435,889-69,540,420 , GRCh38.p12 chr4: 68,570,171-68,674,702	UGT2B17, LOC100422402, 3 more genes
nsv4379490	copy number variation	34	nstd173	human		GRCh37 chr11: 55,376,649-55,442,305 , GRCh38.p12 chr11: 55,609,173-55,674,829	OR4C6, OR4S2, 2 more genes
nsv4366437	copy number variation	2	nstd173	human		GRCh37 chr6: 257,049-291,070 , GRCh38.p12 chr6: 257,049-291,070	, DUSP22, 1 more genes
nsv4376806	copy number variation	247	nstd173	human		GRCh37 chr12: 11,219,930-11,247,388 , GRCh38.p12 chr12: 11,067,331-11,094,789	PRH1, PRH1-PRR4, 3 more genes
nsv4385127	copy number variation	2	nstd173	human		GRCh37 chr5: 17,513,397-17,687,853 , GRCh38.p12 chr5: 17,513,288-17,687,744	TAF11L6, H3P19, 8 more genes
nsv4374520	copy number variation	35	nstd173	human		GRCh37 chr5: 8,702,522-8,747,232 , GRCh38.p12 chr5: 8,702,410-8,747,120	0
nsv4386306	copy number variation	141	nstd173	human		GRCh37 chrX: 924,088-944,608 , GRCh38.p12 chrX: 963,353-983,873	0
nsv4365447	copy number variation	2	nstd173	human		GRCh37 chr14: 22,594,507-22,966,418 , GRCh38.p12 chr14: 22,126,549-22,497,433	TRAJ60, TRDC, 53 more genes
nsv4376337	copy number variation	2	nstd173	human		GRCh37 chr19: 53,930,304-54,016,460 , GRCh38.p12 chr19: 53,427,051-53,513,206	TPM3P6, RPL39P37, 8 more genes
nsv4369792	copy number variation	4	nstd173	human		GRCh37 chrX: 94,344,023-94,391,887 , GRCh38.p12 chrX: 95,089,024-95,136,888	0
nsv4386410	copy number variation	1	nstd173	human		GRCh37 chrX: 134,923,683-134,947,982 , GRCh38.p12 chr: NaN-NaN	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

2-1502-003 AND nstd173 (18)
dbVar

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)