pcdh18[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
nsv3917126	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 116,630,862-145,429,900 , NCBI36 chr4: 117,771,466-146,570,502 , GRCh37 chr4: 117,552,018-146,351,052	PCDH18, SETD7, 294 more genes
nsv3874323	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 126,549,693-141,313,049 , GRCh38.p12 chr4: 125,628,538-140,391,895	PCDH18, FTH1P24, 127 more genes
nsv3912421	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 129,260,477-143,571,978 , GRCh37 chr4: 129,041,027-143,352,528 , GRCh38 chr4: 128,119,872-142,431,375	PCDH18, PCDH10-DT, 120 more genes
nsv6291168	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 138,289,049-145,923,298 , GRCh38.p12 chr4: 137,367,895-145,002,146	PCDH18, LOC105377447, 92 more genes
nsv6290718	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 136,529,470-141,564,812 , GRCh38.p12 chr4: 135,608,315-140,643,658	PCDH18, MGARP, 61 more genes
nsv4674743	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 137,901,978-141,527,647 , GRCh38.p12 chr4: 136,980,824-140,606,493	PCDH18, RAB33B-AS1, 56 more genes
nsv3873978	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 11,525-191,028,879 , GRCh38.p12 chr4: 11,525-190,107,724	PCDH18, LOC100422029, 2358 more genes
nsv3876533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-190,963,766 , GRCh38.p12 chr4: 49,556-190,042,611	PCDH18, LOC100420289, 2347 more genes
nsv3884499	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 12,440-190,904,441 , GRCh38.p12 chr4: 12,440-189,983,286	PCDH18, MTND4LP29, 2341 more genes
nsv3880085	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr4: 68,346-190,957,473 , GRCh38.p12 chr4: 68,454-190,036,318	PCDH18, LOC112268460, 2345 more genes
nsv3883791	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-190,915,650 , GRCh38.p12 chr4: 49,556-189,994,495	PCDH18, LOC105377343, 2341 more genes
nsv3875534	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 93,071,152-190,957,473 , GRCh38.p12 chr4: 92,150,001-190,036,318	PCDH18, KLKB1, 1118 more genes
nsv6291432	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354	PCDH18, SNHG27, 1091 more genes
nsv3874596	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 109,199,664-189,752,726 , GRCh38.p12 chr4: 108,278,508-188,831,572	PCDH18, RPL6P12, 938 more genes
nsv3924008	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 118,065,569-190,042,639 , GRCh37 chr4: 118,986,724-190,828,225 , NCBI36 chr4: 119,206,172-191,200,788	PCDH18, PPID, 828 more genes
nsv3874610	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 119,437,495-190,904,301 , GRCh38.p12 chr4: 118,516,340-189,983,146	PCDH18, OTUD4, 813 more genes
nsv3918110	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 122,658,828-191,220,419 , GRCh38 chr4: 121,518,223-190,062,270 , GRCh37 chr4: 122,439,378-190,828,225	PCDH18, SCRG1, 770 more genes
nsv4455301	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 124,873,497-185,278,662 , GRCh38.p12 chr4: 123,952,342-184,357,509	PCDH18, SMARCA5, 633 more genes
nsv3911855	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 125,432,943-185,761,887 , GRCh37 chr4: 126,354,098-186,683,041 , NCBI36 chr4: 126,573,548-186,920,035	PCDH18, RPL26P16, 656 more genes
nsv3911177	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 131,985,253-190,095,391 , NCBI36 chr4: 133,125,858-191,250,527 , GRCh37 chr4: 132,906,408-190,828,225	PCDH18, SNORD73B, 683 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 28

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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