cmc1[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
nsv3918687	copy number variation	1	nstd102	human	Benign	NCBI36 chr9: 79,632,869-79,650,572 , GRCh37 chr9: 80,443,049-80,460,752 , GRCh38 chr9: 77,828,133-77,845,836	GNAQ
nsv3894189	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 80,646,484-80,647,412 , GRCh38.p12 chr9: 78,031,568-78,032,496	GNAQ
nsv4728180	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 28,255,118-28,311,631 , GRCh38.p12 chr3: 28,213,627-28,270,140	CMC1
nsv3891761	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 80,322,373-80,644,551 , GRCh38.p12 chr9: 77,707,457-78,029,635	GNAQ, LOC107987081
nsv3897053	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 68,999,534-84,656,998 , GRCh38.p12 chr9: 40,926,305-82,042,083	PABIR1, LINC01507, 397 more genes
nsv3893036	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 68,838,523-83,340,723 , GRCh38.p12 chr9: 40,915,719-80,725,808	RPL35AP21, RNU6-599P, 379 more genes
nsv6311966	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 16,710,965-41,275,270 , GRCh38.p12 chr3: 16,669,458-41,233,779	CMC1, LOC102724104, 291 more genes
nsv3915174	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 70,304,266-85,474,962 , GRCh38 chr9: 68,499,530-83,670,227 , GRCh37 chr9: 71,130,848-86,285,142	LOC107987086, PGM5, 183 more genes
nsv4455928	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 70,974,661-81,829,792 , GRCh38.p12 chr9: 68,359,745-79,214,877	RPL35AP21, LOC105376097, 134 more genes
nsv3904790	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 74,534,790-84,014,155 , GRCh38.p12 chr9: 71,919,874-81,399,240	LOC105376099, LOC107987082, 108 more genes
nsv3913411	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 75,511,422-82,175,364 , GRCh37 chr9: 76,321,602-82,985,544 , GRCh38 chr9: 73,706,686-80,370,629	OTX2P1, RPSAP9, 72 more genes
nsv6312943	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 79,792,621-80,944,002 , GRCh38.p12 chr9: 77,177,705-78,329,086	RPL21P84, GNA14-AS1, 14 more genes
nsv3885606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156	CMC1, RNU4-62P, 2880 more genes
nsv3889228	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115	CMC1, NDUFB4, 2876 more genes
nsv3880617	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391	CMC1, RPL23AP49, 2875 more genes
nsv3912247	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 2,934-140,273,252 , GRCh37.p13 chr9: 12,934-141,153,431 , GRCh38.p12 chr9: 12,934-138,262,981	ALOX15P2, LOC107987061, 2184 more genes
nsv3890420	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,122,247 , GRCh38.p12 chr9: 10,590-138,231,797	TBC1D13, LOC105376186, 2183 more genes
nsv3905118	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,114,095 , GRCh38.p12 chr9: 10,590-138,223,645	MIR219A2, CLCN3P1, 2183 more genes
nsv3891842	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,107,672 , GRCh38.p12 chr9: 10,590-138,217,222	OR13C1P, CDC37L1, 2183 more genes
nsv3895453	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 46,587-141,066,491 , GRCh38.p12 chr9: 46,587-138,172,039	RPL19P15, SPATA31D5P, 2176 more genes

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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 68

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Number of Variants: 20

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