picalm[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
nsv3892765	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 85,642,444-85,685,166 , GRCh38.p12 chr11: 85,931,401-85,974,123	PICALM, SLC25A1P1
nsv3908642	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 85,475,317-85,681,916 , GRCh38.p12 chr11: 85,764,274-85,970,873	PICALM, SYTL2, 3 more genes
nsv5380796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397	PICALM, FAUP4, 2031 more genes
nsv3904761	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 80,053,454-113,316,236 , GRCh38.p12 chr11: 80,342,410-113,445,514	PICALM, RPS6P16, 449 more genes
nsv3913977	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 77,943,882-106,650,146 , GRCh38 chr11: 78,232,836-106,779,420 , NCBI36 chr11: 77,621,530-106,155,356	PICALM, PLS1P1, 349 more genes
nsv6637396	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 81,478,509-104,667,040 , GRCh38.p12 chr11: 81,767,467-104,796,313	PICALM, LOC107984375, 295 more genes
nsv3921121	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 75,941,754-98,357,960 , NCBI36 chr11: 75,330,446-97,733,898 , GRCh37 chr11: 75,652,798-98,228,688	PICALM, LOC105369441, 296 more genes
nsv6313961	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 77,855,209-98,002,445 , GRCh38.p12 chr11: 78,144,163-98,131,717	PICALM, MTND5P38, 252 more genes
nsv3922508	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 85,242,847-102,920,097 , GRCh37 chr11: 84,953,891-102,738,968 , NCBI36 chr11: 84,631,539-102,296,037	PICALM, AMOTL1, 240 more genes
nsv3897292	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 80,318,996-96,116,221 , GRCh38.p12 chr11: 80,607,952-96,383,057	PICALM, FAM181B, 218 more genes
nsv3901209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 81,771,852-90,851,187 , GRCh38.p12 chr11: 82,060,810-91,118,019	PICALM, RPL7AP54, 124 more genes
nsv6637847	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 80,562,738-88,663,067 , GRCh38.p12 chr11: 80,851,695-88,929,899	PICALM, PRSS23, 92 more genes
nsv4674839	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 83,530,179-87,059,742 , GRCh38.p12 chr11: 83,819,136-87,348,700	PICALM, LOC100420680, 44 more genes
nsv3877607	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 83,315,294-86,755,595 , GRCh38.p12 chr11: 83,604,251-87,044,553	PICALM, OR7E13P, 43 more genes
nsv7094111	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 85,339,652-86,666,127 , GRCh38.p12 chr11: 85,628,608-86,955,085	PICALM, PRSS23, 30 more genes
nsv3893233	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576	PICALM, LOC105376598, 2842 more genes
nsv3900144	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169	PICALM, RTN3, 2833 more genes
nsv3908873	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576	PICALM, IGHMBP2, 2829 more genes
nsv6315537	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576	PICALM, PYGM, 2125 more genes
nsv3898361	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 71,588,805-116,680,918 , GRCh38.p12 chr11: 71,877,759-116,810,202	PICALM, SESN3, 694 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 32

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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