pcf11[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
nsv3874130	copy number variation	1	nstd102	human	not provided	GRCh38 chr11: 83,147,625-83,165,228 , GRCh37 chr11: 82,858,667-82,876,270	PCF11
nsv3877668	copy number variation	1	nstd102	human	not provided	GRCh38 chr11: 83,154,476-83,165,228 , GRCh37 chr11: 82,865,518-82,876,270	PCF11
esv3648586	copy number variation	1	estd216	human	not provided	GRCh37 chr11: 82,858,667-82,876,270 , GRCh38.p12 chr11: 83,147,625-83,165,228	PCF11
esv3648588	copy number variation	1	estd216	human	not provided	GRCh37 chr11: 82,865,518-82,876,270 , GRCh38.p12 chr11: 83,154,476-83,165,228	PCF11
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	PCF11, 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	PCF11, 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	PCF11, 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	PCF11, 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	PCF11, 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	PCF11, MTND5P38, 252 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	PCF11, 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	PCF11, 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	PCF11, PRSS23, 92 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	PCF11, 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	PCF11, 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	PCF11, 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	PCF11, 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	PCF11, SESN3, 694 more genes
nsv3921008	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 77,750,902-85,554,070 , GRCh38 chr11: 78,362,208-86,165,380 , GRCh37 chr11: 78,073,254-85,876,422	PCF11, CCDC83, 70 more genes
nsv4675911	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 82,788,438-82,910,068 , GRCh38.p12 chr11: 83,077,396-83,199,026	PCF11, PCF11-AS1, 5 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 24

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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