clp1[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	USP14, THOC1, 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	THOC1, USP14, 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	THOC1, LOC107985155, 2 more genes
nsv6309117	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 57,365,055-57,428,908 , GRCh38.p12 chr11: 57,597,582-57,661,436	CLP1, MIR130A, 2 more genes
nsv5380796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397	CLP1, FAUP4, 2031 more genes
nsv3911811	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577	PRPSAP1, CACNG1, 1350 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	LOC101927410, APCDD1, 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	ANKRD12, DLGAP1-AS1, 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	RNA5SP449, MPPE1, 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	RNU7-25P, RPL6P27, 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	LOC100533852, LINC01906, 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	PRELID3A, ANKRD30B, 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	LOC100419892, LOC107985173, 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	LOC105372003, YES1, 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	PRELID3A, LOC646203, 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	LOC107985155, LOC646203, 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	ANKRD62, LOC100419892, 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	LOC105371975, RN7SL50P, 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	EIF4A2P1, PMM2P2, 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	RNU6-324P, RNU1-109P, 263 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 174

Page of 9

Number of Variants: 20

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