14-0258-004 AND nstd173 - dbVar - NCBI

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

Search results

Items: 14

loading data ...

Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4367014	copy number variation	172	nstd173	human		GRCh37 chr6: 78,969,104-79,035,184 , GRCh38.p12 chr6: 78,259,387-78,325,467	LOC105377865
nsv4380290	copy number variation	32	nstd173	human		GRCh37 chr6: 81,274,336-81,294,386 , GRCh38.p12 chr6: 80,564,619-80,584,669	LOC112267962
nsv4372198	copy number variation	20	nstd173	human		GRCh37 chr6: 124,435,286-124,470,365 , GRCh38.p12 chr6: 124,114,141-124,149,220	NKAIN2
nsv4365999	copy number variation	1	nstd173	human		GRCh37 chr12: 85,906,037-86,069,997 , GRCh38.p12 chr12: 85,512,259-85,676,219	LINC02820, LOC101059974
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
nsv4370464	copy number variation	362	nstd173	human		GRCh37 chr11: 4,967,239-4,991,060 , GRCh38.p12 chr11: 4,946,009-4,969,830	OR51A4, OR51A2
nsv4368962	copy number variation	1	nstd173	human		GRCh37 chr5: 75,833,647-75,914,307 , GRCh38.p12 chr5: 76,537,822-76,618,482	LOC101929109, F2RL2, 1 more genes
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
nsv4383855	copy number variation	44	nstd173	human		GRCh37 chrX: 103,259,181-103,312,921 , GRCh38.p12 chrX: 104,004,609-104,058,356	H2BW2, LOC107985662, 1 more genes
nsv4366691	copy number variation	623	nstd173	human		GRCh37 chr4: 69,435,901-69,485,978 , GRCh38.p12 chr4: 68,570,183-68,620,260	UGT2B17, LOC100422402, 1 more genes
nsv4366876	copy number variation	3	nstd173	human		GRCh37 chr14: 74,006,838-74,031,034 , GRCh38.p12 chr14: 73,540,134-73,564,330	ACOT1, HEATR4, 1 more genes
nsv4387956	copy number variation	9	nstd173	human		GRCh37 chr14: 106,560,963-106,777,343 , GRCh38.p12 chr14: 106,112,755-106,321,086	IGHV3-13, IGHV3-19, 30 more genes
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
nsv4387494	copy number variation	1	nstd173	human		GRCh37 chrX: 58,504,038-58,527,176 , GRCh38.p12 chrX: 58,477,605-58,500,743	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

14-0258-004 AND nstd173 (15)
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)