colec12[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
nsv3889364	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr18: 163,323-376,355 , GRCh38 chr18: 163,327-376,359	COLEC12, USP14, 1 more genes
nsv4457516	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr18: 136,226-475,796 , GRCh38.p12 chr18: 136,226-475,796	COLEC12, THOC1, 3 more genes
nsv6637690	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr18: 220,341-556,146 , GRCh38.p12 chr18: 220,341-556,146	COLEC12, THOC1, 2 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	COLEC12, 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	COLEC12, 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	COLEC12, 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	COLEC12, 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	COLEC12, 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	COLEC12, 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	COLEC12, 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	COLEC12, 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	COLEC12, 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	COLEC12, 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	COLEC12, 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	COLEC12, 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	COLEC12, 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	COLEC12, 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	COLEC12, 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	COLEC12, 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	COLEC12, 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 145

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Number of Variants: 20

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