letm1[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
nsv3910998	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr4: 1,796,826-1,830,551 , GRCh37 chr4: 1,827,028-1,860,753 , GRCh38 chr4: 1,825,301-1,859,026	LETM1
nsv3911788	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 1,814,763-1,850,806 , GRCh38 chr4: 1,813,036-1,849,079 , NCBI36 chr4: 1,784,561-1,820,604	LETM1
nsv3874961	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 1,809,650-1,865,381 , GRCh38.p12 chr4: 1,807,923-1,863,654	LETM1, FGFR3
nsv3871888	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr4: 1,784,694-1,919,793 , GRCh38.p12 chr4: 1,782,967-1,918,066	LETM1, FGFR3, 2 more genes
nsv3877925	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 1,742,616-1,816,281 , GRCh38.p12 chr4: 1,740,889-1,814,554	LETM1, FGFR3, 2 more genes
nsv4728898	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 1,778,534-1,912,732 , GRCh38.p12 chr4: 1,776,807-1,911,005	LETM1, NSD2, 2 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	LETM1, 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	LETM1, 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	LETM1, 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	LETM1, 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	LETM1, 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	LETM1, 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	LETM1, 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	LETM1, 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	LETM1, 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	LETM1, 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	LETM1, 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	LETM1, 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	LETM1, 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	LETM1, USP17L21, 318 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 143

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Number of Variants: 20

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Supplemental Content

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