2-1169-001 AND nstd173 - dbVar - NCBI

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

Search results

Items: 12

loading data ...

Number of Variants: 12

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4384091	copy number variation	77	nstd173	human		GRCh37 chr11: 49,710,704-49,746,720 , GRCh38.p12 chr11: 49,689,152-49,725,168 , GRCh38.p12 chr11\|NW_019805495.1: 153,334-179,145	GRM5P1
nsv4371901	copy number variation	1	nstd173	human		GRCh37 chr9: 15,339,722-15,390,258 , GRCh38.p12 chr9: 15,339,724-15,390,260	RPL7P33
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
nsv4383110	copy number variation	1	nstd173	human		GRCh37 chr17: 6,794,301-6,865,997 , GRCh38.p12 chr17: 6,890,982-6,962,678	ALOX12P2, SPICP3
nsv4372991	copy number variation	1	nstd173	human		GRCh37 chr3: 144,006,519-144,286,898 , GRCh38.p12 chr3: 144,287,677-144,568,056	LOC105374140,
nsv4365991	copy number variation	13	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	LOC105378797, RPL31P12
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
nsv4377875	copy number variation	73	nstd173	human		GRCh37 chr5: 180,375,302-180,430,797 , GRCh38.p12 chr5: 180,948,302-181,003,797	BTNL8, BTNL3, 3 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
nsv4374133	copy number variation	39	nstd173	human		GRCh37 chr3: 175,883,703-175,916,315 , GRCh38.p12 chr3: 176,165,915-176,198,527 , GRCh38.p12 chr3\|NW_019805488.1: 50,426-83,038	0
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
nsv4385903	copy number variation	1	nstd173	human		GRCh37 chr14: 22,730,241-22,938,126 , GRCh38.p12 chr14: 22,262,357-22,469,134	TRDJ2, TRDD2, 20 more genes

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

2-1169-001 AND nstd173 (13)
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)