SP50580 AND nstd71 - 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
nsv880749	copy number variation	21	nstd71	human		NCBI36 chr4: 162,058,162-162,146,977 , GRCh37.p13 chr4: 161,838,712-161,927,527 , GRCh38.p12 chr4: 160,917,560-161,006,375	LOC105377513
nsv872108	copy number variation	59	nstd71	human		NCBI36 chr1: 105,833,927-106,065,063 , GRCh37.p13 chr1: 106,032,404-106,263,540 , GRCh38.p12 chr1: 105,489,782-105,720,918	LOC105378881, SEPTIN2P1, 2 more genes
nsv879310	copy number variation	1929	nstd71	human		NCBI36 chr4: 69,076,346-69,179,871 , GRCh37.p13 chr4: 69,393,751-69,497,276 , GRCh38.p12 chr4: 68,528,033-68,631,558	LOC100422402, LOC100132651, 2 more genes
nsv871196	copy number variation	88	nstd71	human		NCBI36 chr1: 12,777,429-12,810,136 , GRCh37.p13 chr1: 12,854,842-12,887,549 , GRCh38.p12 chr1: 12,794,693-12,827,690	PRAMEF11, PRAMEF1, 1 more genes
nsv914688	copy number variation	8	nstd71	human		NCBI36 chr22: 23,991,725-24,145,104 , GRCh37.p13 chr22: 25,661,725-25,815,104 , GRCh38.p12 chr22: 25,265,758-25,419,137	LOC100419673, LOC105372969, 2 more genes
nsv911348	copy number variation	463	nstd71	human		NCBI36 chr19: 20,386,247-20,520,617 , GRCh37.p13 chr19\|NW_003571053.2: 329,860-463,224 , GRCh37.p13 chr19: 20,522,409-20,728,777 , GRCh38.p12 chr19: 20,411,600-20,545,971	BNIP3P23, LOC105372317, 4 more genes
nsv906133	copy number variation	3	nstd71	human		NCBI36 chr16: 32,437,365-32,449,148 , GRCh37.p13 chr16: 32,529,864-32,541,647 , GRCh38.p12 chr16: 32,518,543-32,530,326	0
nsv906401	copy number variation	15	nstd71	human		NCBI36 chr16: 32,469,358-32,475,644 , GRCh37.p13 chr16: 32,561,857-32,568,143 , GRCh38.p12 chr16: 32,550,536-32,556,822	0
nsv896349	copy number variation	30	nstd71	human		NCBI36 chr10: 135,102,337-135,235,772 , GRCh37.p13 chr10: 135,252,347-135,385,782 , GRCh38.p12 chr10: 133,438,843-133,572,278	CYP2E1, OR7M1P, 6 more genes
nsv896955	copy number variation	127	nstd71	human		NCBI36 chr11: 5,828,407-5,911,385 , GRCh37.p13 chr11: 5,871,831-5,954,809 , GRCh38.p12 chr11: 5,850,601-5,933,579	OR52E7P, OR52E4, 4 more genes
nsv893369	copy number variation	1	nstd71	human		NCBI36 chr9: 66,345,398-66,834,318 , GRCh37.p13 chr9: 66,605,578-67,094,498 , GRCh38.p12 chr: NaN-NaN	0
nsv914924	copy number variation	3	nstd71	human		NCBI36 chr22: 24,208,614-24,258,620 , GRCh37.p13 chr22: 25,878,614-25,928,620 , GRCh38.p12 chr22: 25,482,647-25,532,653	0
nsv884869	copy number variation	4	nstd71	human		NCBI36 chr6: 32,565,228-32,586,132 , GRCh37.p13 chr6: 32,457,250-32,478,154 , GRCh38.p12 chr6: 32,489,473-32,510,377	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

SP50580 AND nstd71 (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)