pcdhgb5[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
nsv3889848	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719	PCDHGB5, MEGF10, 2080 more genes
nsv3884357	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 86,400,000-154,000,000 , GRCh38.p12 chr5: 87,104,183-154,620,440	PCDHGB5, TXNDC15, 962 more genes
nsv3912937	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 105,955,289-155,551,397 , NCBI36 chr5: 105,983,188-155,483,975 , GRCh38 chr5: 106,619,588-156,124,387	PCDHGB5, LINC01023, 783 more genes
nsv3924309	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 138,206,826-145,191,872 , GRCh38 chr5: 138,871,137-145,812,309 , NCBI36 chr5: 138,234,725-145,172,065	PCDHGB5, FCHSD1, 183 more genes
nsv3872314	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 139,147,238-141,540,491 , GRCh38.p12 chr5: 139,767,653-142,160,926	PCDHGB5, VTRNA1-1, 122 more genes
nsv3886374	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028	PCDHGB5, LOC105374618, 2499 more genes
nsv3871533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343	PCDHGB5, PCDHGC5, 2492 more genes
nsv3875235	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788	PCDHGB5, SPEF2, 2490 more genes
nsv3874238	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 106,716,357-180,687,338 , GRCh38.p12 chr5: 107,380,656-181,260,337	PCDHGB5, PJA2, 1228 more genes
nsv3878636	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 130,125,085-157,574,910 , GRCh38.p12 chr5: 130,789,392-158,147,902	PCDHGB5, LOC100288484, 551 more genes
nsv3923414	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 130,196,621-154,701,371 , NCBI36 chr5: 130,224,520-154,681,564 , GRCh38 chr5: 130,860,928-155,321,811	PCDHGB5, HNRNPA3P7, 514 more genes
nsv3914009	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 129,211,386-152,713,299 , GRCh38 chr5: 129,847,794-153,353,546 , GRCh37 chr5: 129,183,487-152,733,106	PCDHGB5, UQCRQ, 489 more genes
nsv3924856	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 140,449,756-148,890,434 , GRCh37 chr5: 140,469,572-148,910,241 , GRCh38 chr5: 141,089,988-149,530,678	PCDHGB5, CTB-99A3.1, 160 more genes
nsv6636181	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr5: 140,865,418-140,865,497 , GRCh38 chr5: 141,485,851-141,485,930	PCDHGB5, PCDHGC3, 20 more genes
nsv3912182	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr5: 138,306,445-143,964,773 , GRCh37.p13 chr5: 138,278,546-143,984,580 , GRCh38.p12 chr5: 138,942,857-144,605,017	PCDHGB5, CD14, 176 more genes
nsv3884275	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr5: 94,844,077-178,830,410 , GRCh38.p12 chr5: 95,508,373-179,403,409	PCDHGB5, LOC107986368, 1258 more genes
nsv3875894	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr5: 140,676,272-140,929,172 , GRCh38.p12 chr5: 141,296,707-141,549,605	PCDHGB5, PCDHGA6, 27 more genes
nsv4436202	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379	PCDHGB5, RNU1-150P, 1757 more genes
nsv3918788	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr5: 140,322,968-141,682,547 , GRCh38 chr5: 140,963,199-142,322,798 , GRCh37 chr5: 140,453,735-141,702,363	PCDHGB5, PCDHB2, 86 more genes
nsv3912593	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259	PCDHGB5, LOC105378993, 2492 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 23

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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