gpat2[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
nsv3906443	copy number variation	1	nstd102	human	Benign	NCBI36 chr2: 96,035,699-96,068,780 , GRCh37 chr2: 96,671,972-96,705,053 , GRCh38 chr2: 96,006,224-96,039,305	GPAT2, FAHD2CP
nsv3910630	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331	GPAT2, DAZAP2P1, 2991 more genes
nsv6634330	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419	GPAT2, CYP1B1-AS1, 1649 more genes
nsv4452469	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 96,552,903-98,118,115 , GRCh38.p12 chr2: 95,887,155-97,501,652	GPAT2, CNNM4, 47 more genes
nsv3902782	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 95,879,602-97,285,797 , GRCh37 chr2: 96,545,350-98,013,866 , NCBI36 chr2: 95,909,077-97,380,005	GPAT2, SNRNP200, 39 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	GPAT2, LOC112268439, 3737 more genes
nsv3874648	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305	GPAT2, IGKV2OR2-10, 3737 more genes
nsv3885544	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609	GPAT2, RNU6-674P, 3735 more genes
nsv3882615	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232	GPAT2, MTND2P22, 3724 more genes
nsv3876227	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 96,353,030-114,045,463 , GRCh38.p12 chr2: 95,687,282-113,287,886	GPAT2, RNU4-8P, 346 more genes
nsv3902899	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 94,707,984-111,076,455 , GRCh38 chr2: 94,678,532-110,602,409 , GRCh37 chr2: 95,344,257-111,359,986	GPAT2, MTCO3P45, 325 more genes
nsv3877583	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 95,529,039-108,518,266 , GRCh38.p12 chr2: 94,863,294-107,901,810	GPAT2, RPL27AP4, 242 more genes
nsv3906654	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 91,443,218-102,334,856 , NCBI36 chr2: 90,981,410-102,317,748 , GRCh37 chr2: 91,617,683-102,951,316	GPAT2, CHEK2P3, 197 more genes
nsv3899291	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 95,618,109-103,868,854 , GRCh38 chr2: 94,817,406-103,252,396 , NCBI36 chr2: 94,846,878-103,235,286	GPAT2, IGKV2OR2-10, 178 more genes
nsv3889077	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 95,691,600-100,587,394 , GRCh38.p12 chr2: 95,025,855-99,970,932	GPAT2, TMEM127, 114 more genes
nsv3891473	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	NCBI36 chr2: 95,909,077-97,059,136 , GRCh38 chr2: 95,879,602-97,029,672 , GRCh37 chr2: 96,545,350-97,695,409	GPAT2, ADRA2B, 33 more genes
nsv6314726	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196	GPAT2, ACTG2, 1713 more genes
nsv6636315	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr2: 95,341,388-100,340,514 , GRCh38.p12 chr2: 94,675,663-99,724,052	GPAT2, ADRA2B, 130 more genes
nsv3882113	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr2: 96,468,158-97,871,906 , GRCh38.p12 chr2: 95,802,410-97,206,169	GPAT2, ADRA2B, 39 more genes
nsv3895360	copy number variation	1	nstd102	human	Benign	NCBI36 chr2: 95,704,456-96,081,750 , GRCh37 chr2: 96,340,729-96,718,023 , GRCh38 chr2: 95,674,981-96,052,275	GPAT2, ANKRD36C, 5 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 44

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Number of Variants: 20

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