ppp2r2d[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
nsv3906845	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 133,733,922-133,973,625 , GRCh38.p12 chr10: 131,920,418-132,160,121	PPP2R2D, JAKMIP3, 1 more genes
nsv3921209	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr10: 131,448,228-131,943,718 , GRCh37 chr10: 133,246,491-133,757,222 , NCBI36 chr10: 133,136,481-133,607,212	PPP2R2D, LINC01164, 3 more genes
nsv3920511	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 133,255,624-133,728,500 , GRCh38 chr10: 131,457,361-131,922,234 , NCBI36 chr10: 133,145,614-133,585,728	PPP2R2D, LOC105378565, 3 more genes
nsv3915089	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr10: 133,255,652-133,728,500 , NCBI36 chr10: 133,145,642-133,585,670 , GRCh38 chr10: 131,457,389-131,922,176	PPP2R2D, LOC105378566, 3 more genes
nsv3902530	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr10: 133,536,778-133,753,668 , GRCh38.p12 chr10: 131,704,442-131,940,164	PPP2R2D, LINC01164, 3 more genes
nsv3902548	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 133,657,703-133,766,057 , GRCh38.p12 chr10: 131,825,367-131,952,553	PPP2R2D, LOC105378566, 2 more genes
nsv3917672	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 133,246,515-133,757,222 , NCBI36 chr10: 133,136,505-133,607,212 , GRCh38 chr10: 131,448,252-131,943,718	PPP2R2D, LOC105378565, 3 more genes
nsv3915755	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr10: 133,366,855-133,585,611 , GRCh37.p13 chr10: 133,516,865-133,735,621 , GRCh38.p12 chr10: 131,684,529-131,922,117	PPP2R2D, LINC01164, 3 more genes
nsv7137209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639	PPP2R2D, RNU7-12P, 1876 more genes
nsv3920295	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 81,675,342-135,374,737 , GRCh37.p13 chr10: 81,685,362-135,524,747 , GRCh38.p12 chr10: 79,925,606-133,787,422	PPP2R2D, EIF2S2P3, 895 more genes
nsv3909943	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 122,213,942-135,434,178 , GRCh38 chr10: 120,454,430-133,620,674 , NCBI36 chr10: 122,203,932-135,284,168	PPP2R2D, TEX36-AS1, 198 more genes
nsv3892639	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 122,443,197-135,477,883 , GRCh38.p12 chr10: 120,683,685-133,740,558	PPP2R2D, OR6L2P, 208 more genes
nsv3896819	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 122,343,861-135,427,143 , GRCh38.p12 chr10: 120,584,349-133,613,639	PPP2R2D, MMP21, 198 more genes
nsv3906646	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 122,509,781-135,427,143 , GRCh38.p12 chr10: 120,750,269-133,613,639	PPP2R2D, LOC105378560, 196 more genes
nsv7098893	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 122,610,933-135,439,810 , GRCh38.p12 chr10: 120,851,421-133,626,306	PPP2R2D, LOC105378571, 196 more genes
nsv3919728	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 120,970,558-133,622,588 , NCBI36 chr10: 122,720,061-135,286,082 , GRCh37 chr10: 122,730,071-135,436,092	PPP2R2D, BANF1P2, 194 more genes
nsv5980446	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 122,785,023-135,457,222 , GRCh38.p12 chr10: 121,025,510-133,643,718	PPP2R2D, LINC02641, 194 more genes
nsv3909245	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 123,019,239-135,427,143 , GRCh38.p12 chr10: 121,259,725-133,613,639	PPP2R2D, LOC105378565, 187 more genes
nsv3921792	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 123,338,496-135,284,168 , GRCh37 chr10: 123,348,506-135,434,178 , GRCh38 chr10: 121,588,992-133,620,674	PPP2R2D, LINC02641, 185 more genes
nsv7137208	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 123,477,898-135,427,143 , GRCh38.p12 chr10: 121,718,384-133,613,639	PPP2R2D, ZRANB1, 182 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 113

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Number of Variants: 20

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