OAT_07 AND nstd53 - dbVar - NCBI

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

Search results

Items: 13

loading data ...

Number of Variants: 13

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv870374	copy number variation	79	nstd53	human		NCBI36 chr1: 72,541,502-72,589,682 , GRCh38.p12 chr1: 72,303,231-72,351,411 , GRCh37.p13 chr1: 72,768,914-72,817,094 , GRCh38.p12 chr1\|NW_018654707.1: 15,498-72,636	LOC105378797
nsv870244	copy number variation	26	nstd53	human		NCBI36 chr7: 141,408,072-141,438,504 , GRCh37.p13 chr7: 141,761,603-141,792,035 , GRCh38.p12 chr7: 142,061,803-142,092,235 , GRCh38.p12 chr7\|NT_187562.1: 23,683-54,115 , GRCh37.p13 chr7\|NW_003571040.1: 203,754-234,186	MGAM
nsv869729	copy number variation	57	nstd53	human		NCBI36 chr1: 150,823,126-150,848,509 , GRCh38.p12 chr1: 152,584,026-152,609,409 , GRCh37.p13 chr1: 152,556,502-152,581,885	LCE3C
nsv869907	copy number variation	1	nstd53	human		NCBI36 chr14: 102,437,834-102,455,572 , GRCh38.p12 chr14: 102,901,744-102,919,482 , GRCh37.p13 chr14: 103,368,081-103,385,819	TRAF3
nsv869943	copy number variation	10	nstd53	human		GRCh37.p13 chr3: 46,792,820-46,854,438 , GRCh38.p12 chr3: 46,751,330-46,812,948 , NCBI36 chr3: 46,767,824-46,829,442	PRSS44P, PRSS43P
nsv869963	copy number variation	2	nstd53	human		NCBI36 chr16: 66,942,907-66,972,404 , GRCh38.p12 chr16: 68,351,503-68,381,000 , GRCh37.p13 chr16: 68,385,406-68,414,903	PRMT7, SMPD3
nsv870151	copy number variation	2	nstd53	human		NCBI36 chr16: 1,089,425-1,157,497 , GRCh38.p12 chr16: 1,099,424-1,167,496 , GRCh37.p13 chr16: 1,149,424-1,217,496	CACNA1H, LOC105371042, 1 more genes
nsv869847	copy number variation	2	nstd53	human		NCBI36 chr22: 18,592,279-18,618,206 , GRCh38.p12 chr22: 20,224,756-20,250,683 , GRCh37.p13 chr22: 20,212,279-20,238,206	RTN4R, MIR1286, 2 more genes
nsv869711	copy number variation	90	nstd53	human		NCBI36 chr4: 69,099,876-69,643,272 , GRCh37.p13 chr: NaN-NaN , GRCh38.p12 chr: NaN-NaN	0
nsv869772	copy number variation	1	nstd53	human		NCBI36 chr14: 18,798,700-19,467,512 , GRCh38.p12 chr14: 18,907,993-19,259,006 , GRCh37.p13 chr14: 19,728,700-20,397,672	BMS1P18, OR11H13P, 17 more genes
nsv870413	copy number variation	41	nstd53	human		GRCh38.p12 chr2: 34,472,710-34,513,110 , NCBI36 chr2: 34,551,281-34,591,681 , GRCh37.p13 chr2: 34,697,777-34,738,177	0
nsv869852	copy number variation	1	nstd53	human		NCBI36 chr17: 77,602,536-77,671,235 , GRCh37.p13 chr17: 80,009,247-80,077,946 , GRCh38.p12 chr17: 82,051,371-82,120,070	FASN, GPS1, 4 more genes
nsv870006	copy number variation	1	nstd53	human		NCBI36 chr14: 105,630,148-105,843,086 , GRCh38.p12 chr14: 106,112,755-106,315,778 , GRCh37.p13 chr14: 106,559,103-106,772,041	IGH, IGHVIII-26-1, 29 more genes

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

OAT_07 AND nstd53 (14)
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)