mustn1[All Fields] AND 1[has_clinical] - 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
nsv3875047	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 52,086,599-59,689,209 , GRCh38.p12 chr3: 52,052,583-59,703,483	MUSTN1, SLMAP, 132 more genes
nsv3912778	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 49,498,433-55,348,528 , GRCh38 chr3: 49,461,000-55,314,500 , NCBI36 chr3: 49,473,437-55,323,568	MUSTN1, SEMA3G, 160 more genes
nsv4453518	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 52,195,134-52,869,037 , GRCh38.p12 chr3: 52,161,118-52,835,021	MUSTN1, SNORD19B, 42 more genes
nsv3885606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156	MUSTN1, RNU4-62P, 2880 more genes
nsv3889228	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115	MUSTN1, NDUFB4, 2876 more genes
nsv3880617	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391	MUSTN1, RPL23AP49, 2875 more genes
nsv4347762	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 45,153,770-53,878,616 , GRCh38.p12 chr3: 45,112,278-53,844,589	MUSTN1, UQCRC1, 291 more genes
nsv3917135	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr3: 51,406,905-55,073,516 , GRCh37 chr3: 51,431,865-55,098,476 , GRCh38 chr3: 51,394,434-55,064,449	MUSTN1, ACY1, 96 more genes
nsv7096813	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 52,018,081-53,845,433 , GRCh38.p12 chr3: 51,984,065-53,811,406	MUSTN1, DNAH1, 62 more genes
nsv7097206	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 52,109,903-53,164,416 , GRCh38.p12 chr3: 52,075,887-53,130,400	MUSTN1, PHF7, 47 more genes
nsv4673975	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 51,247,306-53,069,942 , GRCh38.p12 chr3: 51,209,875-53,035,926	MUSTN1, RRP9, 76 more genes
nsv6636925	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 52,780,509-53,418,869 , GRCh38.p12 chr3: 52,746,493-53,384,842	MUSTN1, LOC105377094, 17 more genes
nsv6636758	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 52,783,975-53,418,893 , GRCh38.p12 chr3: 52,749,959-53,384,866	MUSTN1, NEK4, 17 more genes

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

mustn1[All Fields] AND 1[has_clinical] (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)