nr2c2[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
nsv6315249	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 13,371,737-20,095,506 , GRCh37.p13 chr3: 13,413,237-20,136,998	NR2C2, RNU6-905P, 99 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	NR2C2, 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	NR2C2, 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	NR2C2, 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	NR2C2, 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	NR2C2, 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	NR2C2, 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	NR2C2, 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	NR2C2, 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	NR2C2, 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	NR2C2, 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	NR2C2, 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	NR2C2, 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	NR2C2, TAMM41, 267 more genes
nsv3885029	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 1,897,972-19,519,085 , GRCh38.p12 chr3: 1,856,288-19,477,593	NR2C2, VGLL4, 247 more genes
nsv3883804	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 5,173,870-16,760,262 , GRCh38.p12 chr3: 5,132,185-16,718,755	NR2C2, JAGN1, 200 more genes
nsv6634367	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 13,836,340-25,357,427 , GRCh38.p12 chr3: 13,794,843-25,315,936	NR2C2, TMEM43, 132 more genes
nsv3888298	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 13,276,005-24,295,240 , GRCh38.p12 chr3: 13,234,505-24,253,749	NR2C2, NR1D2, 134 more genes
nsv3919322	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 14,360,747-21,656,134 , GRCh37 chr3: 14,402,247-21,697,626 , NCBI36 chr3: 14,377,251-21,672,630	NR2C2, LOC105376988, 89 more genes
nsv3888438	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr3: 13,720,222-17,808,236 , GRCh38.p12 chr3: 13,678,723-17,766,744	NR2C2, BTD, 70 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 22

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Number of Variants: 20

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Supplemental Content

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