crtc3[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
nsv3900831	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 91,219,451-91,222,139 , GRCh38.p12 chr15: 90,676,220-90,678,908	CRTC3-AS1
nsv4681036	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 91,259,558-91,359,692 , GRCh38.p12 chr15: 90,716,327-90,816,462	CRTC3-AS1, BLM
nsv6637618	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 91,217,953-91,398,682 , GRCh38.p12 chr15: 90,674,722-90,855,452	CRTC3-AS1, LOC105370969, 2 more genes
nsv4456493	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 91,243,790-91,403,844 , GRCh38.p12 chr15: 90,700,559-90,860,614	BLM, RN7SL363P, 2 more genes
nsv3916249	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189	CRTC3, H3P40, 1616 more genes
nsv3919468	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189	CRTC3, RNU6-18P, 1442 more genes
nsv4729092	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 86,962,053-102,531,392 , GRCh38.p12 chr15: 86,418,822-101,981,189	CRTC3, CHD2, 272 more genes
nsv4675149	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 87,189,245-102,429,112 , GRCh38.p12 chr15: 86,646,014-101,888,909	CRTC3, TTLL13, 264 more genes
nsv3908429	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 90,346,994-102,354,798 , GRCh38.p12 chr15: 89,803,763-101,814,595	CRTC3, RPL31P55, 201 more genes
nsv4350274	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 83,883,823-92,165,844 , GRCh38.p12 chr15: 83,215,071-91,622,614	CRTC3, AKAP13, 184 more genes
nsv6290316	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 88,465,861-94,411,846 , GRCh38.p12 chr15: 87,922,630-93,868,617	CRTC3, LOC105370964, 130 more genes
nsv3902841	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 88,295,992-94,215,607 , GRCh38.p12 chr15: 87,752,761-93,672,378	CRTC3, BLM, 129 more genes
nsv6291795	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 89,520,451-93,926,491 , GRCh38.p12 chr15: 88,977,220-93,383,262	CRTC3, LINC00930, 106 more genes
nsv4456778	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 91,229,877-93,677,014 , GRCh38.p12 chr15: 90,686,646-93,133,785	H2AZ2P1, MAN2A2, 44 more genes
nsv3900281	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 20,016,811-102,493,540 , GRCh38.p12 chr15: 19,811,558-101,953,337	CRTC3, MYZAP, 1750 more genes
nsv3913581	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 18,323,354-100,338,915 , GRCh37.p13 chr15: 20,063,340-102,521,392 , GRCh38.p12 chr15: 19,858,087-101,981,189	CRTC3, MIR4513, 1754 more genes
nsv3904086	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 20,071,673-102,461,162 , GRCh38.p12 chr15: 19,866,420-101,920,959	CRTC3, TMEM202, 1747 more genes
nsv3905138	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 20,733,395-102,511,616 , GRCh38.p12 chr15: 20,528,156-101,971,413	CRTC3, FES, 1738 more genes
nsv3892955	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr15: 22,770,422-102,429,112 , GRCh38.p12 chr15: 23,319,714-101,888,909	CRTC3, FAM81A, 1614 more genes
nsv3876912	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 31,115,047-102,354,857 , GRCh38.p12 chr15: 30,822,844-101,814,654	CRTC3, RNU6-953P, 1385 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 58

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Number of Variants: 20

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Supplemental Content

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