colca2[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
nsv3902489	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 111,164,420-111,168,024 , GRCh38.p12 chr11: 111,293,695-111,297,299	COLCA1, POU2AF3
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	FAUP4, MMP7, 2031 more genes
nsv3904761	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 80,053,454-113,316,236 , GRCh38.p12 chr11: 80,342,410-113,445,514	RPS6P16, CTSC, 449 more genes
nsv3910101	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 87,796,211-113,996,548 , GRCh37.p13 chr11: 88,156,563-114,491,338 , GRCh38.p12 chr11: 88,423,395-114,620,616	PHB1P16, LOC100418884, 385 more genes
nsv5672640	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976	HSPD1P13, CARD17P, 239 more genes
nsv4455554	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 104,101,411-116,680,918 , GRCh38.p12 chr11: 104,230,683-116,810,202	LINC02732, LINC02698, 198 more genes
nsv4675680	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 103,320,065-114,349,787 , GRCh38.p12 chr11: 103,449,337-114,479,065	DRD2, NCAM1, 181 more genes
nsv4675323	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 105,699,599-114,524,876 , GRCh38.p12 chr11: 105,828,873-114,654,154	RPSAP50, RNA5SP349, 155 more genes
nsv6637811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 109,328,787-116,414,966 , GRCh38.p12 chr11: 109,458,061-116,544,249	LOC102723966, NXPE4, 129 more genes
nsv4683939	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr11: 111,171,709-111,965,694 , GRCh38.p12 chr11: 111,300,984-112,094,970	FDXACB1, LOC107984386, 34 more genes
nsv7093830	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 111,171,709-111,959,745 , GRCh38.p12 chr11: 111,300,984-112,089,021	LOC100132078, DLAT, 34 more genes
nsv7093915	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 111,171,709-111,958,707 , GRCh38.p12 chr11: 111,300,984-112,087,983	CRYAB, BTG4, 34 more genes
nsv3893233	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576	LOC105376598, OSBPL9P2, 2842 more genes
nsv3900144	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169	RTN3, KRTAP5-13P, 2833 more genes
nsv3908873	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576	IGHMBP2, SYTL2, 2829 more genes
nsv6315537	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576	PYGM, ATL3, 2125 more genes
nsv3898361	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 71,588,805-116,680,918 , GRCh38.p12 chr11: 71,877,759-116,810,202	SESN3, LOC107984352, 694 more genes
nsv3922253	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 100,219,331-134,910,140 , NCBI36 chr11: 99,724,541-134,415,350 , GRCh38 chr11: 100,348,599-135,040,246	RPS27P19, UBASH3B, 655 more genes
nsv6289927	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 104,288,964-134,937,416 , GRCh38.p12 chr11: 104,418,236-135,067,522	IGSF9B, MIR10526, 592 more genes
nsv3913577	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 105,972,805-113,384,939 , GRCh37.p13 chr11: 106,467,595-113,879,729 , GRCh38.p12 chr11: 106,596,868-114,009,007	LAYN, DDX10, 133 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 23

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Number of Variants: 20

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Search details

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