mettl4[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
nsv6637695	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr18: 2,280,228-2,555,929 , GRCh38.p12 chr18: 2,280,229-2,555,930	METTL4, LOC105371961
nsv4457763	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr18: 2,481,916-2,639,451 , GRCh38.p12 chr18: 2,481,917-2,639,452	METTL4, KATNBL1P3, 2 more genes
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	METTL4, LOC107985176, 632 more genes
nsv3916217	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 4,275-16,783,904 , GRCh37.p13 chr18: 14,275-18,529,906 , GRCh38.p12 chr18: 14,275-20,949,945	METTL4, LOC101927410, 276 more genes
nsv4676141	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 136,226-18,529,578 , GRCh38.p12 chr18: 136,226-20,949,617	METTL4, ANKRD12, 270 more genes
nsv6290328	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 10,501-15,410,398 , GRCh38.p12 chr18: 10,501-15,410,399	METTL4, RNA5SP449, 275 more genes
nsv7098917	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 1-15,400,035 , GRCh38.p12 chr18: 10,001-15,400,036	METTL4, RNU7-25P, 275 more genes
nsv3905455	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 13,034-15,375,878 , GRCh38.p12 chr18: 13,034-15,375,879	METTL4, LOC100533852, 275 more genes
nsv4676393	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 13,034-15,330,525 , GRCh38.p12 chr18: 13,034-15,330,526	METTL4, PRELID3A, 275 more genes
nsv3898793	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 14,316-15,328,499 , GRCh38.p12 chr18: 14,316-15,328,500	METTL4, LOC100419892, 275 more genes
nsv3907765	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 1-15,157,836 , GRCh38.p12 chr18: 10,001-15,157,837	METTL4, LOC105372003, 269 more genes
nsv3896525	copy number variation	5	nstd102	human	Pathogenic	GRCh37 chr18: 136,226-15,198,990 , GRCh38.p12 chr18: 136,226-15,198,991	METTL4, PRELID3A, 264 more genes
nsv3897591	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 136,226-15,198,989 , GRCh38.p12 chr18: 136,226-15,198,990	METTL4, LOC107985155, 264 more genes
nsv4348774	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 136,226-15,175,005 , GRCh38.p12 chr18: 136,226-15,175,006	METTL4, ANKRD62, 263 more genes
nsv3908226	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 13,034-15,026,309 , GRCh38.p12 chr18: 13,034-15,026,310	METTL4, LOC105371975, 269 more genes
nsv4676314	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 136,304-15,143,714 , GRCh38.p12 chr18: 136,304-15,143,715	METTL4, EIF4A2P1, 263 more genes
nsv3911263	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 131,700-15,121,054 , NCBI36 chr18: 121,700-15,111,054 , GRCh38 chr18: 131,700-15,121,055	METTL4, RNU6-324P, 263 more genes
nsv3916675	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 48,782-14,978,075 , NCBI36 chr18: 38,782-14,968,075 , GRCh38 chr18: 48,782-14,978,076	METTL4, L3MBTL4, 265 more genes
nsv3924580	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr18: 118,760-15,024,003 , GRCh37 chr18: 118,760-15,024,002 , NCBI36 chr18: 108,760-15,014,002	METTL4, LOC105371951, 264 more genes
nsv3890222	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 136,226-14,983,938 , GRCh38.p12 chr18: 136,226-14,983,939	METTL4, LOC105371986, 261 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 128

Page of 7

Number of Variants: 20

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Search details

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