ccdc80[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
nsv7148201	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 93,979,547-124,774,010 , GRCh37.p13 chr3: 93,698,391-124,492,857	CCDC80, NECTIN3, 418 more genes
nsv3918661	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 95,088,205-124,418,220 , GRCh37 chr3: 93,605,515-122,935,530 , GRCh38 chr3: 93,886,671-123,216,683	CCDC80, MTCO2P29, 401 more genes
nsv3917160	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 95,021,157-118,088,593 , GRCh38 chr3: 93,819,623-116,887,056 , GRCh37 chr3: 93,538,467-116,605,903	CCDC80, ATP6V1A, 297 more genes
nsv3910775	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 97,514,213-115,382,196 , GRCh38 chr3: 97,795,369-115,663,349 , NCBI36 chr3: 98,996,903-116,864,886	CCDC80, ZBTB11-AS1, 258 more genes
nsv3918094	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 113,822,514-129,935,667 , GRCh38 chr3: 112,620,977-128,734,134 , GRCh37 chr3: 112,339,824-128,452,977	CCDC80, QTRT2, 284 more genes
nsv3911662	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 102,633,427-117,731,277 , GRCh37.p13 chr3: 101,150,737-116,248,587 , GRCh38.p12 chr3: 101,431,893-116,529,740	CCDC80, SIDT1, 188 more genes
nsv3888585	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 105,094,834-117,441,953 , GRCh38.p12 chr3: 105,375,990-117,723,106	CCDC80, RFKP2, 165 more genes
nsv6315408	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 106,598,767-115,704,696 , GRCh38.p12 chr3: 106,879,920-115,985,849	CCDC80, DZIP3, 138 more genes
nsv6636830	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 107,059,705-115,005,256 , GRCh38.p12 chr3: 107,340,858-115,286,409	CCDC80, ATP6V1A, 117 more genes
nsv3913048	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 109,444,109-117,370,868 , GRCh38 chr3: 108,242,572-116,169,331 , GRCh37 chr3: 107,961,419-115,888,178	CCDC80, RPSAP29, 115 more genes
nsv3911341	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 113,722,090-121,232,559 , GRCh38 chr3: 112,520,553-120,031,022 , GRCh37 chr3: 112,239,400-119,749,869	CCDC80, ZNF80, 103 more genes
nsv3913239	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 111,887,676-117,112,203 , GRCh38 chr3: 112,168,829-117,393,356 , NCBI36 chr3: 113,370,366-118,594,893	CCDC80, SNORD155, 73 more genes
nsv3887339	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 111,894,832-116,930,109 , GRCh38.p12 chr3: 112,175,985-117,211,262	CCDC80, MIR8076, 72 more genes
nsv7098849	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 110,943,783-115,859,912 , GRCh38.p12 chr3: 111,224,936-116,141,065	CCDC80, ATG3, 81 more genes
nsv3876262	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 110,645,295-115,103,586 , GRCh38.p12 chr3: 110,926,448-115,384,739	CCDC80, C3orf52, 77 more genes
nsv3910502	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 113,612,063-117,037,810 , GRCh37.p13 chr3: 112,129,373-115,555,120 , GRCh38.p12 chr3: 112,410,526-115,836,273	CCDC80, EIF4E2P2, 53 more genes
nsv3912427	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 112,425,234-115,795,585 , GRCh37 chr3: 112,144,081-115,514,432 , NCBI36 chr3: 113,626,771-116,997,122	CCDC80, CD200R1L-AS1, 51 more genes
nsv3871257	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 112,144,081-115,514,432 , GRCh38.p12 chr3: 112,425,234-115,795,585	CCDC80, SLC35A5, 51 more genes
nsv3924149	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 113,666,631-116,975,648 , GRCh38 chr3: 112,465,094-115,774,111 , GRCh37 chr3: 112,183,941-115,492,958	CCDC80, ATOSBP1, 51 more genes
nsv4578248	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 112,183,943-115,492,949 , GRCh38.p12 chr3: 112,465,096-115,774,102	CCDC80, ZBTB20, 51 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 32

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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