clec14a[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
nsv3919982	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr14: 38,088,975-38,648,187 , GRCh37 chr14: 38,558,180-39,117,391 , NCBI36 chr14: 37,627,931-38,187,142	CLEC14A, LOC112268136, 2 more genes
nsv4675285	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 38,538,434-39,127,208 , GRCh38.p12 chr14: 38,069,229-38,658,004	CLEC14A, LOC100422334, 2 more genes
nsv6314715	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 21,162,263-50,713,602 , GRCh38.p12 chr14: 20,694,104-50,246,884	CLEC14A, HNRNPC, 616 more genes
nsv3916277	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr14: 19,734,944-44,823,755 , GRCh38 chr14: 20,196,945-45,284,802 , GRCh37 chr14: 20,665,104-45,754,005	CLEC14A, MIR208B, 600 more genes
nsv3917157	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 24,018,169-42,452,605 , GRCh38 chr14: 23,548,960-41,983,402 , NCBI36 chr14: 23,088,009-41,522,355	CLEC14A, LINC02300, 274 more genes
nsv3916173	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr14: 33,118,898-48,418,573 , GRCh37.p13 chr14: 34,049,147-49,348,823 , GRCh38.p12 chr14: 33,579,941-48,879,620	CLEC14A, TTC6, 178 more genes
nsv3924751	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 31,261,477-45,154,334 , GRCh38 chr14: 30,792,271-44,685,131 , NCBI36 chr14: 30,331,228-44,224,084	CLEC14A, DNAJC8P1, 171 more genes
nsv3895946	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 35,934,503-47,120,961 , GRCh38.p12 chr14: 35,465,297-46,651,758	CLEC14A, PRPF39-DT, 121 more genes
nsv5381757	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 33,608,925-44,570,367 , GRCh38.p12 chr14: 33,139,719-44,101,164	CLEC14A, RPLP0P3, 131 more genes
nsv3921024	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 35,537,482-44,463,980 , GRCh38 chr14: 35,068,276-43,994,777 , NCBI36 chr14: 34,607,233-43,533,730	CLEC14A, LOC107984681, 101 more genes
nsv3912278	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 33,880,412-42,359,485 , NCBI36 chr14: 33,419,369-41,898,438 , GRCh37 chr14: 34,349,618-42,828,688	CLEC14A, RPL23AP8, 120 more genes
nsv4676032	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 36,830,396-42,541,277 , GRCh38.p12 chr14: 36,361,190-42,072,074	CLEC14A, PPIAP4, 60 more genes
nsv6313916	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 36,862,276-41,597,549 , GRCh38.p12 chr14: 36,393,071-41,128,344	CLEC14A, LOC105370462, 55 more genes
nsv3921621	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 36,434,568-41,102,476 , GRCh37 chr14: 36,903,773-41,571,681 , NCBI36 chr14: 35,973,524-40,641,431	CLEC14A, LOC105370456, 54 more genes
nsv3891331	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 35,850,213-40,138,562 , GRCh38.p12 chr14: 35,381,007-39,669,358	CLEC14A, LOC105370452, 70 more genes
nsv3902883	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,000,422-107,289,053 , GRCh38.p12 chr14: 18,223,945-106,880,863	CLEC14A, LOC440181, 1998 more genes
nsv3907460	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,280,733-107,287,663 , GRCh38.p12 chr14: 18,504,256-106,879,456	CLEC14A, BANF1P1, 1996 more genes
nsv3899639	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,327,823-107,287,663 , GRCh38.p12 chr14: 18,551,346-106,879,456	CLEC14A, LOC100289511, 1996 more genes
nsv3903256	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,794,561-107,234,280 , GRCh38.p12 chr14: 19,652,445-106,826,050	CLEC14A, DHRS7, 1946 more genes
nsv3919106	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,511,673-107,285,437 , GRCh38 chr14: 20,043,514-106,877,229 , NCBI36 chr14: 19,581,513-106,356,482	CLEC14A, SRMP2, 1929 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 33

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Number of Variants: 20

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