pparg[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
nsv3880764	copy number variation	1	nstd102	human	Benign	GRCh37 chr3: 12,401,414-12,411,238 , GRCh38.p12 chr3: 12,359,915-12,369,739	PPARG
nsv3875306	copy number variation	1	nstd102	human	Benign	GRCh37 chr3: 12,316,770-12,360,769 , GRCh38.p12 chr3: 12,275,271-12,319,270	PPARG
nsv3905232	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 32,241-12,681,483 , GRCh37 chr3: 73,914-12,722,982 , NCBI36 chr3: 48,914-12,697,982	PPARG, OR7E122P, 163 more genes
nsv3885461	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,891-12,575,409 , GRCh38.p12 chr3: 20,213-12,533,910	PPARG, MARK2P14, 160 more genes
nsv3880780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 8,922,160-12,338,637 , GRCh38.p12 chr3: 8,880,476-12,297,138	PPARG, IL17RC, 77 more genes
nsv7148081	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 10,167,260-12,533,766 , GRCh38.p12 chr3: 10,125,576-12,492,267	PPARG, SLC6A1-AS1, 37 more genes
nsv6291061	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 10,922,740-12,456,978 , GRCh38.p12 chr3: 10,881,055-12,415,479	PPARG, TAMM41, 22 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	PPARG, 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	PPARG, 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	PPARG, RPL23AP49, 2875 more genes
nsv3905127	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 94,991-41,423,012 , NCBI36 chr3: 69,991-41,398,016 , GRCh38 chr3: 53,308-41,381,521	PPARG, LINC02022, 540 more genes
nsv3876280	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,891-37,459,464 , GRCh38.p12 chr3: 20,213-37,417,973	PPARG, OXTR, 460 more genes
nsv3892895	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 52,266-37,148,076 , GRCh37 chr3: 93,949-37,189,567 , NCBI36 chr3: 68,949-37,164,571	PPARG, RPL34P11, 452 more genes
nsv3878718	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,891-36,710,181 , GRCh38.p12 chr3: 20,213-36,668,690	PPARG, LRRC3B, 436 more genes
nsv3875913	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,891-33,958,201 , GRCh38.p12 chr3: 20,213-33,916,709	PPARG, RPS27P11, 424 more genes
nsv3901059	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 73,914-30,105,699 , GRCh38 chr3: 32,241-30,064,208 , NCBI36 chr3: 48,914-30,080,703	PPARG, RPL32, 369 more genes
nsv3923656	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 11,463,328-38,919,543 , NCBI36 chr3: 11,479,802-38,936,038 , GRCh37 chr3: 11,504,802-38,961,034	PPARG, RN7SL4P, 348 more genes
nsv3875223	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,891-24,432,821 , GRCh38.p12 chr3: 20,213-24,391,330	PPARG, XPC-AS1, 311 more genes
nsv3904668	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 48,914-20,350,883 , GRCh37 chr3: 73,914-20,375,879 , GRCh38 chr3: 32,241-20,334,387	PPARG, C3orf20, 281 more genes
nsv3907461	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 63,843-19,510,600 , GRCh37 chr3: 105,526-19,552,092 , NCBI36 chr3: 80,526-19,527,096	PPARG, TAMM41, 267 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 26

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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