ccdc68[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
nsv6314722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 1,262,334-53,254,751 , GRCh38.p12 chr18: 1,262,333-55,587,520	CCDC68, LOC107985176, 632 more genes
nsv3902831	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 46,177,798-78,014,123 , GRCh38.p12 chr18: 48,651,427-80,256,240	CCDC68, LOC105372180, 370 more genes
nsv3906152	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 46,942,427-78,014,123 , GRCh38.p12 chr18: 49,416,057-80,256,240	CCDC68, RPL17P44, 360 more genes
nsv3909519	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 47,656,799-78,014,123 , GRCh38.p12 chr18: 50,130,429-80,256,240	CCDC68, LOC105372160, 339 more genes
nsv3920508	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr18: 51,167,159-80,256,240 , GRCh37 chr18: 48,693,529-78,014,123 , NCBI36 chr18: 46,947,527-76,115,097	CCDC68, LOC105372152, 319 more genes
nsv3916196	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 48,716,799-78,010,032 , GRCh38 chr18: 51,190,429-80,252,149 , NCBI36 chr18: 46,970,797-76,111,023	CCDC68, LOC105372200, 319 more genes
nsv4676105	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 49,460,596-78,014,123 , GRCh38.p12 chr18: 51,934,226-80,256,240	CCDC68, MIR548AV, 310 more genes
nsv3914571	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 49,947,422-78,012,829 , NCBI36 chr18: 48,201,420-76,113,817 , GRCh38 chr18: 52,421,052-80,254,946	CCDC68, RPS2P6, 308 more genes
nsv3918507	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr18: 53,865,057-80,252,149 , GRCh37 chr18: 51,391,427-78,010,032 , NCBI36 chr18: 49,645,425-76,111,023	CCDC68, NETO1, 303 more genes
nsv3918799	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 47,937,267-61,226,978 , GRCh38 chr18: 52,156,899-65,408,762 , GRCh37 chr18: 49,683,269-63,075,998	CCDC68, LOC105372121, 157 more genes
nsv3896853	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 50,739,715-63,705,988 , GRCh38.p12 chr18: 53,213,345-66,038,752	CCDC68, MALT1-AS1, 158 more genes
nsv3904776	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 51,036,415-59,275,480 , GRCh38.p12 chr18: 53,510,045-61,608,247	CCDC68, RPL29P32, 110 more genes
nsv3923854	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 50,675,985-56,408,844 , GRCh38 chr18: 54,857,756-60,590,631 , GRCh37 chr18: 52,524,987-58,257,864	CCDC68, ZNF532, 90 more genes
nsv6314029	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 50,707,829-54,924,248 , GRCh38.p12 chr18: 53,181,459-57,257,017	CCDC68, RNA5SP459, 42 more genes
nsv3920675	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 47,655,796-51,477,228 , GRCh38 chr18: 51,875,428-55,658,999 , GRCh37 chr18: 49,401,798-53,326,230	CCDC68, RPL21P126, 26 more genes
nsv3920403	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 50,248,665-51,767,238 , GRCh37 chr18: 51,994,667-53,616,240 , GRCh38 chr18: 54,468,297-55,949,009	CCDC68, MIR4529, 17 more genes
nsv3915222	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr18: 54,291,850-55,754,281 , GRCh37 chr18: 51,818,220-53,421,512 , NCBI36 chr18: 50,072,218-51,572,510	CCDC68, LINC03035, 18 more genes
nsv6637722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 52,023,322-53,332,606 , GRCh38.p12 chr18: 54,496,952-55,665,375	CCDC68, LINC03035, 13 more genes
nsv6315530	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271	CCDC68, LOC105372145, 947 more genes
nsv3907444	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 12,842-78,015,180 , GRCh38.p12 chr18: 12,842-80,257,297	CCDC68, GALNT1, 947 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 60

Page of 3

Number of Variants: 20

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Supplemental Content

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