cdh15[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3919939	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 87,748,226-87,789,395 , GRCh37 chr16: 89,220,725-89,261,894 , GRCh38 chr16: 89,154,317-89,195,486	CDH15, SLC22A31, 3 more genes
nsv3904036	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 89,249,149-89,336,307 , GRCh38.p12 chr16: 89,182,741-89,269,899	CDH15, ANKRD11, 2 more genes
nsv3903662	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 89,234,948-89,273,092 , GRCh38.p12 chr16: 89,168,540-89,206,684	CDH15, ZNF778, 2 more genes
nsv6637473	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 89,255,096-89,321,089 , GRCh38.p12 chr16: 89,188,688-89,254,681	CDH15, ZNF778, 1 more genes
nsv4457551	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 89,255,518-89,320,845 , GRCh38.p12 chr16: 89,189,110-89,254,437	CDH15, ZNF778, 1 more genes
nsv3877297	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 86,890,893-89,398,630 , GRCh38.p12 chr16: 86,857,287-89,332,222	CDH15, LOC112268182, 68 more genes
nsv3917970	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 86,950,106-89,335,814 , NCBI36 chr16: 85,541,213-87,929,723 , GRCh37 chr16: 86,983,712-89,402,222	CDH15, ZNF778, 68 more genes
nsv3879843	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 87,183,661-89,520,803 , GRCh38.p12 chr16: 87,150,055-89,454,395	CDH15, LOC100287036, 68 more genes
nsv3913039	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 87,306,529-89,269,079 , GRCh37 chr16: 87,340,135-89,335,487 , NCBI36 chr16: 85,897,636-87,862,988	CDH15, ZNF778, 61 more genes
nsv3885545	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 87,340,135-89,335,428 , GRCh38.p12 chr16: 87,306,529-89,269,020	CDH15, GALNS, 61 more genes
nsv3899619	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,116,155-89,524,926 , GRCh38.p12 chr16: 88,082,549-89,458,518	CDH15, PIEZO1, 47 more genes
nsv3920773	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,193,266-89,572,450 , NCBI36 chr16: 86,750,767-88,099,951 , GRCh38 chr16: 88,159,660-89,506,042	CDH15, LOC101930112, 48 more genes
nsv6315145	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,365,786-89,584,412 , GRCh38.p12 chr16: 88,332,180-89,518,004	CDH15, SPG7, 46 more genes
nsv4456065	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,453,448-89,569,215 , GRCh38.p12 chr16: 88,387,040-89,502,807	CDH15, LOC101927863, 45 more genes
nsv3876943	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,230,760-89,363,742 , GRCh38.p12 chr16: 88,197,154-89,297,334	CDH15, LINC02138, 40 more genes
nsv3874480	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,230,961-89,363,602 , GRCh38.p12 chr16: 88,197,355-89,297,194	CDH15, CTU2, 40 more genes
nsv3877335	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,556,191-89,557,911 , GRCh38.p12 chr16: 88,489,783-89,491,503	CDH15, SNAI3-AS1, 42 more genes
nsv3871782	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,635,000-89,628,950 , GRCh38.p12 chr16: 88,568,592-89,562,542	CDH15, LOC339059, 41 more genes
nsv3877060	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,630,607-89,607,742 , GRCh38.p12 chr16: 88,564,199-89,541,334	CDH15, LOC339059, 39 more genes
nsv3913965	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,706,524-89,596,883 , GRCh38 chr16: 88,640,116-89,530,475 , NCBI36 chr16: 87,234,025-88,124,384	CDH15, LOC100129697, 38 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 103

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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