cct7[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
nsv3871942	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 92,177,723-92,298,111 , GRCh38.p12 chr5: 92,842,016-92,962,404	CCT7P2, LDHBP3, 1 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	CCT7, DAZAP2P1, 2991 more genes
nsv3889848	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719	MEGF10, LOC100128407, 2080 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	CCT7, CYP1B1-AS1, 1649 more genes
nsv3912840	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 144,764,751-247,199,719 , GRCh37.p13 chr1: 146,053,394-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643	CRB1, STX6, 1608 more genes
nsv3884357	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 86,400,000-154,000,000 , GRCh38.p12 chr5: 87,104,183-154,620,440	TXNDC15, PCDHAC1, 962 more genes
nsv3915450	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 90,707,525-130,655,256 , NCBI36 chr5: 90,743,281-130,683,155 , GRCh38 chr5: 91,411,708-131,319,563	MCTP1, LOC102467217, 422 more genes
nsv3916468	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 89,670,423-127,412,115 , GRCh38 chr5: 90,374,606-128,076,423 , NCBI36 chr5: 89,706,179-127,440,014	LOC105379149, LOC107986365, 406 more genes
nsv3924896	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 84,603,580-111,435,081 , GRCh37 chr5: 83,899,398-110,770,779 , NCBI36 chr5: 83,935,154-110,798,678	LOC107986438, GGCTP1, 254 more genes
nsv3914008	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 88,377,169-104,022,949 , NCBI36 chr5: 88,412,925-104,050,848 , GRCh38 chr5: 89,081,352-104,687,248	LOC105379080, LOC105379100, 166 more genes
nsv3921368	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 86,672,700-100,860,147 , NCBI36 chr5: 86,708,456-100,888,046 , GRCh38 chr5: 87,376,883-101,524,443	LOC107986438, MTCO1P22, 158 more genes
nsv3879974	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 91,504,101-104,858,348 , GRCh38.p12 chr5: 92,208,284-105,522,647	LOC105379090, LNPEP, 142 more genes
nsv3891146	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 139,513,020-150,389,231 , GRCh38.p12 chr6: 139,191,883-150,068,095	UST, RAET1K, 131 more genes
nsv3890752	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 144,075,695-152,337,005 , GRCh38.p12 chr6: 143,754,558-152,015,870	LOC105378052, RNU6-302P, 109 more genes
nsv3920651	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 144,932,561-152,985,364 , NCBI36 chr6: 145,295,390-153,348,192 , GRCh37 chr6: 145,253,697-153,306,499	PPP1R14C, RAET1K, 107 more genes
nsv3874231	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 87,512,314-95,096,562 , GRCh38.p12 chr5: 88,216,497-95,760,858	ARRDC3, LOC107986433, 71 more genes
nsv3912526	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 91,386,552-98,365,880 , NCBI36 chr5: 90,718,125-97,729,488 , GRCh37 chr5: 90,682,369-97,701,584	RTRAFP2, RHOBTB3, 77 more genes
nsv3903429	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 144,126,513-147,699,831 , GRCh38 chr1: 143,515,074-149,563,337 , GRCh37 chr1: 145,415,156-149,433,207	PDZK1, LOC105369140, 216 more genes
nsv7148188	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 88,189,536-93,784,597 , GRCh37.p13 chr5: 87,485,353-93,120,303	RPS3AP22, LOC105379078, 49 more genes
nsv3892632	copy number variation	4	nstd102	human	Pathogenic	GRCh37 chr1: 145,747,242-149,155,026 , GRCh38 chr1: 143,515,074-149,076,087 , NCBI36 chr1: 144,458,599-147,421,650	LOC728989, MIR6077, 205 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 86

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Number of Variants: 20

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