col27a1[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
nsv7098419	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 116,917,341-116,918,270 , GRCh38.p12 chr9: 114,155,061-114,155,990	COL27A1
nsv6312677	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr9: 117,044,259-117,046,337 , GRCh38.p12 chr9: 114,281,979-114,284,057	COL27A1
nsv7098050	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 117,037,921-117,072,975 , GRCh38.p12 chr9: 114,275,641-114,310,695	COL27A1, LOC105376224
nsv7098420	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 117,046,993-117,072,977 , GRCh38.p12 chr9: 114,284,713-114,310,697	COL27A1, LOC105376224
nsv7097683	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 117,050,715-117,072,975 , GRCh38.p12 chr9: 114,288,435-114,310,695	COL27A1, LOC105376224
nsv3891722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 104,604,851-126,253,089 , GRCh38.p12 chr9: 101,842,569-123,490,810	COL27A1, LOC107987013, 326 more genes
nsv3917989	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 102,112,198-118,529,754 , NCBI36 chr9: 101,152,019-117,569,575 , GRCh38 chr9: 99,349,916-115,767,475	COL27A1, CTNNAL1, 262 more genes
nsv3922633	copy number variation	2	nstd102	human	Pathogenic	GRCh38 chr9: 99,138,048-115,011,033 , NCBI36 chr9: 100,940,151-116,813,133 , GRCh37 chr9: 101,900,330-117,773,312	COL27A1, RAD23B, 262 more genes
nsv3891066	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 113,083,182-126,779,494 , GRCh38.p12 chr9: 110,320,902-124,017,215	COL27A1, FKBP15, 211 more genes
nsv3911862	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 109,332,416-119,768,043 , GRCh38 chr9: 107,530,314-117,965,944 , GRCh37 chr9: 110,292,595-120,728,222	COL27A1, RPL36AP6, 164 more genes
nsv3904811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 114,299,780-123,267,736 , GRCh38.p12 chr9: 111,537,500-120,505,458	COL27A1, FAM225B, 121 more genes
nsv3892176	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 111,348,809-118,687,200 , GRCh38.p12 chr9: 108,586,529-115,924,921	COL27A1, AKNA, 124 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	COL27A1, ALOX15P2, 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	COL27A1, TBC1D13, 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	COL27A1, MIR219A2, 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	COL27A1, OR13C1P, 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	COL27A1, RPL19P15, 2176 more genes
nsv3900967	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 163,131-141,122,114 , GRCh38.p12 chr9: 163,131-138,231,664	COL27A1, BANCR, 2173 more genes
nsv3907479	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 62,525-141,006,407 , GRCh38.p12 chr9: 62,525-138,111,955	COL27A1, OR2AM1P, 2174 more genes
nsv3922684	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897	COL27A1, TDRD7, 2170 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 48

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Number of Variants: 20

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