1-1023-003 AND nstd173 - dbVar - NCBI

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

Search results

Items: 15

loading data ...

Number of Variants: 15

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
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
nsv4377927	copy number variation	1	nstd173	human		GRCh37 chr15: 53,782,801-53,885,049 , GRCh38.p12 chr15: 53,490,604-53,592,852	WDR72, LOC105370826
nsv4382531	copy number variation	1	nstd173	human		GRCh37 chr16: 6,981,577-7,062,445 , GRCh38.p12 chr16: 6,931,576-7,012,444	RNU6-328P, RBFOX1
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
nsv4378486	copy number variation	188	nstd173	human		GRCh37 chr1: 248,753,184-248,795,289 , GRCh38.p12 chr1: 248,589,883-248,631,988	OR2T10, OR2T11
nsv4371377	copy number variation	2	nstd173	human		GRCh37 chr19: 41,345,315-41,380,870 , GRCh38.p12 chr19: 40,839,410-40,874,965	CYP2A7, CYP2A6
nsv4380515	copy number variation	77	nstd173	human		GRCh37 chr12: 8,558,475-8,594,982 , GRCh38.p12 chr12: 8,405,879-8,442,386	OR7E148P, OR7E149P, 1 more genes
nsv4369627	copy number variation	2	nstd173	human		GRCh37 chr15: 24,350,856-24,782,266 , GRCh38.p12 chr15: 24,105,709-24,537,119	PWRN2, PWRN3, 4 more genes
nsv4368822	copy number variation	4	nstd173	human		GRCh37 chr14: 34,951,774-35,020,972 , GRCh38.p12 chr14: 34,482,568-34,551,766	RNU1-27P, EAPP, 4 more genes
nsv4366546	copy number variation	98	nstd173	human		GRCh37 chr3: 162,524,824-162,626,676 , GRCh38.p12 chr3: 162,807,036-162,908,888	0
nsv4376970	copy number variation	5	nstd173	human		GRCh37 chr13: 84,101,178-84,161,129 , GRCh38.p12 chr13: 83,527,043-83,586,994	0
nsv4368957	copy number variation	3	nstd173	human		GRCh37 chrX: 93,338,568-93,382,086 , GRCh38.p12 chrX: 94,083,569-94,127,087	0
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
nsv4373999	copy number variation	2	nstd173	human		GRCh37 chr14: 22,689,703-22,960,757 , GRCh38.p12 chr14: 22,221,804-22,491,770	TRAJ50, TRDV3, 38 more genes
nsv4374126	copy number variation	35	nstd173	human		GRCh37 chr5: 57,326,267-57,349,970 , GRCh38.p12 chr5: 58,030,440-58,054,143	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

1-1023-003 AND nstd173 (16)
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)