ccdc88a[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
nsv7096176	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 55,544,322-55,546,160 , GRCh38.p12 chr2: 55,317,186-55,319,024	CCDC88A
nsv6311595	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr2: 55,558,401-55,561,804 , GRCh38.p12 chr2: 55,331,265-55,334,668	CCDC88A
nsv7096670	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 55,518,847-55,523,679 , GRCh38.p12 chr2: 55,291,711-55,296,543	CCDC88A
nsv6311515	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 55,522,713-55,527,057 , GRCh38.p12 chr2: 55,295,577-55,299,921	CCDC88A
nsv7096515	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 55,459,961-55,646,215 , GRCh38.p12 chr2: 55,232,825-55,419,079	CCDC88A, MTIF2, 3 more genes
nsv7096893	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 55,459,961-55,616,042 , GRCh38.p12 chr2: 55,232,825-55,388,906	CCDC88A, MTIF2, 3 more genes
nsv7096669	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 55,459,961-55,566,804 , GRCh38.p12 chr2: 55,232,825-55,339,668	CCDC88A, RPS27A, 3 more genes
nsv3910630	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331	CCDC88A, DAZAP2P1, 2991 more genes
nsv6634330	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419	CCDC88A, CYP1B1-AS1, 1649 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	CCDC88A, LOC112268439, 3737 more genes
nsv3874648	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305	CCDC88A, IGKV2OR2-10, 3737 more genes
nsv3885544	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609	CCDC88A, RNU6-674P, 3735 more genes
nsv3882615	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232	CCDC88A, MTND2P22, 3724 more genes
nsv3908605	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 66,097-55,797,773 , GRCh38 chr2: 66,097-55,570,637 , NCBI36 chr2: 56,097-55,651,277	CCDC88A, SLC35F6, 801 more genes
nsv3916821	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 47,701,031-86,783,356 , GRCh37.p13 chr2: 47,847,527-86,929,845 , GRCh38.p12 chr2: 47,620,388-86,702,722	CCDC88A, NAGK, 595 more genes
nsv3875055	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 27,861,707-60,790,985 , GRCh38.p12 chr2: 27,638,840-60,563,850	CCDC88A, RPL7P13, 426 more genes
nsv3882842	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 34,792,916-56,676,541 , GRCh38.p12 chr2: 34,567,849-56,449,406	CCDC88A, STON1, 303 more genes
nsv3905626	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 40,965,422-58,090,956 , GRCh38 chr2: 40,738,282-57,863,821 , NCBI36 chr2: 40,818,926-57,944,460	CCDC88A, RNU6-433P, 220 more genes
nsv6314726	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196	CCDC88A, ACTG2, 1713 more genes
nsv3903805	copy number variation	1	nstd102	human	Benign	GRCh37 chr2: 7,635,254-88,005,418 , NCBI36 chr2: 7,552,705-87,786,533 , GRCh38 chr2: 7,495,123-87,705,899	CCDC88A, LOC101927723, 1246 more genes

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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 30

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Number of Variants: 20

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Supplemental Content

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Search details

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