cand2[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
nsv3887733	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 12,630,912-12,839,915 , GRCh38.p12 chr3: 12,589,413-12,798,416	CRIP1P1, TMEM40, 3 more genes
nsv4449784	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 12,630,912-12,839,659 , GRCh38.p12 chr3: 12,589,413-12,798,160	KRT18P17, RAF1, 3 more genes
nsv3919073	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr3: 12,625,007-12,819,153 , GRCh38 chr3: 12,608,508-12,802,654 , GRCh37 chr3: 12,650,007-12,844,153	CRIP1P1, TMEM40, 3 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	RNU4-62P, SEMA3B-AS1, 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	NDUFB4, LOC105374108, 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	RPL23AP49, DLEC1, 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	LINC02022, RPL23AP43, 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	OXTR, LOC105376944, 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	RPL34P11, RNU1-96P, 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	LRRC3B, CCR4, 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	RPS27P11, LOC107986059, 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	RPL32, RPL15, 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	RN7SL4P, TOP2B, 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	XPC-AS1, LOC101927394, 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	C3orf20, LOC107986059, 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	TAMM41, CYCSP11, 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	VGLL4, RHBDF1P1, 247 more genes
nsv3895908	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 73,914-13,655,318 , NCBI36 chr3: 48,914-13,630,319 , GRCh38 chr3: 32,241-13,613,818	GRM7-AS2, LOC105376949, 180 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	JAGN1, LOC105376944, 200 more genes
nsv3896717	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 7,372,797-14,376,946 , GRCh37 chr3: 7,397,797-14,401,942 , GRCh38 chr3: 7,356,110-14,360,442	OGG1, VN1R20P, 134 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 24

Page of 2

Number of Variants: 20

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Supplemental Content

Find related data

Search details

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