misp3[All Fields] AND 1[has_clinical] - 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
nsv3924466	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 11,496,978-14,126,833 , GRCh38 chr19: 11,525,163-14,155,021 , GRCh37 chr19: 11,635,978-14,265,833	MISP3, JUNB, 135 more genes
nsv3908579	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 14,124,666-16,431,349 , GRCh38.p12 chr19: 14,013,854-16,320,538	MISP3, TMEM167AP2, 99 more genes
nsv3912480	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 12,580,427-14,742,673 , GRCh37 chr19: 12,691,241-14,853,485 , NCBI36 chr19: 12,552,241-14,714,485	MISP3, GET3, 100 more genes
nsv3907864	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 12,574,343-14,726,197 , GRCh38.p12 chr19: 12,463,529-14,615,385	MISP3, WDR83, 105 more genes
nsv3910509	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 13,505,739-15,342,900 , GRCh37 chr19: 13,644,739-15,481,900 , GRCh38 chr19: 13,533,925-15,371,089	MISP3, DDX39A, 76 more genes
nsv3904885	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923	MISP3, ZNF321P, 2443 more genes
nsv3903203	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793	MISP3, BABAM1, 2426 more genes
nsv3903092	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521	MISP3, LENG8, 2408 more genes
nsv3913730	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354	MISP3, BCKDHA, 1102 more genes
nsv3922457	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 14,085,489-28,330,584 , GRCh38 chr19: 13,974,677-27,839,676 , NCBI36 chr19: 13,946,489-33,022,424	MISP3, REX1BD, 416 more genes
nsv3898900	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 9,678,768-14,853,426 , GRCh38.p12 chr19: 9,568,092-14,742,614	MISP3, FBXL12, 253 more genes
nsv3915094	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 12,132,052-14,751,798 , NCBI36 chr19: 12,103,867-14,723,610 , GRCh37 chr19: 12,242,867-14,862,610	MISP3, RN7SL619P, 123 more genes
nsv3891875	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr19: 13,592,592-14,717,528 , GRCh38.p12 chr19: 13,481,778-14,606,716	MISP3, CACNA1A, 48 more genes
nsv3913955	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 13,644,739-14,369,645 , GRCh38 chr19: 13,533,925-14,258,833 , NCBI36 chr19: 13,505,739-14,230,645	MISP3, YJU2B, 30 more genes
nsv3899944	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 11,608,072-14,543,046 , GRCh38.p12 chr19: 11,497,257-14,432,234	MISP3, RNA5SP465, 145 more genes

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

misp3[All Fields] AND 1[has_clinical] (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)