crmp1[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
nsv4456661	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 5,769,949-5,860,325 , GRCh38.p12 chr4: 5,768,222-5,858,598	CRMP1, EVC
nsv3914526	copy number variation	1	nstd102	human	conflicting data from submitters	GRCh38 chr4: 5,802,938-6,159,712 , GRCh37 chr4: 5,804,665-6,161,439 , NCBI36 chr4: 5,855,566-6,212,340	CRMP1, C4orf50, 3 more genes
nsv3877950	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 4,165,334-33,324,781 , GRCh38.p12 chr4: 4,163,607-33,323,159	CRMP1, LOC100418700, 353 more genes
nsv3885762	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 71,552-29,006,745 , GRCh38.p12 chr4: 71,660-29,005,123	CRMP1, CD38, 456 more genes
nsv3923296	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 72,555-28,066,309 , NCBI36 chr4: 62,447-27,677,029 , GRCh37 chr4: 72,447-28,067,931	CRMP1, OR7E99P, 446 more genes
nsv4674378	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-24,280,482 , GRCh38.p12 chr4: 49,556-24,278,859	CRMP1, USP17L30, 394 more genes
nsv6315347	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-20,964,575 , GRCh38.p12 chr4: 68,453-20,962,952	CRMP1, LOC100421802, 375 more genes
nsv6291097	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-20,587,167 , GRCh38.p12 chr4: 68,453-20,585,544	CRMP1, LOC105374479, 372 more genes
nsv3915161	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-20,387,231 , NCBI36 chr4: 58,345-19,996,329 , GRCh38 chr4: 68,453-20,385,608	CRMP1, CTBP1-AS, 370 more genes
nsv1398080	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 44,020-19,796,182 , GRCh38.p12 chr4: 44,019-19,794,559	CRMP1, RPL10AP7, 366 more genes
nsv6112747	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,598-18,912,995 , GRCh38.p12 chr4: 68,706-18,911,372	CRMP1, GPR78, 362 more genes
nsv3915014	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 75,040-17,097,463 , GRCh38 chr4: 85,149-17,486,742 , GRCh37 chr4: 85,040-17,488,365	CRMP1, LOC100422637, 350 more genes
nsv3915275	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 72,447-17,279,636 , GRCh38 chr4: 72,555-17,278,013 , NCBI36 chr4: 62,447-16,888,734	CRMP1, OR7E99P, 347 more genes
nsv3888069	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-15,973,383 , GRCh38.p12 chr4: 68,453-15,971,760	CRMP1, RPS3AP16, 332 more genes
nsv3917860	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 37,335-15,869,056 , NCBI36 chr4: 27,336-15,479,777 , GRCh37 chr4: 37,336-15,870,679	CRMP1, LOC105374338, 330 more genes
nsv3918310	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 72,555-15,658,035 , GRCh37 chr4: 72,447-15,659,658 , NCBI36 chr4: 62,447-15,268,756	CRMP1, RN7SL589P, 323 more genes
nsv3887204	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 71,552-15,302,739 , GRCh38.p12 chr4: 71,660-15,301,115	CRMP1, USP17L21, 318 more genes
nsv3911947	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-14,614,077 , NCBI36 chr4: 58,345-14,223,175 , GRCh38 chr4: 68,453-14,612,453	CRMP1, MIR572, 313 more genes
nsv3914961	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 46,772-14,110,482 , GRCh38 chr4: 56,878-14,499,760 , GRCh37 chr4: 56,772-14,501,384	CRMP1, LOC101928532, 311 more genes
nsv3874716	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-13,770,107 , GRCh38.p12 chr4: 68,453-13,768,483	CRMP1, BOD1L1, 306 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 85

Page of 5

Number of Variants: 20

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Supplemental Content

Find related data

Search details

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