chrm5[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
nsv4675267	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 34,348,337-34,404,263 , GRCh38.p12 chr15: 34,056,136-34,112,062	CHRM5, AVEN, 3 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	CHRM5, 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	CHRM5, RNU6-18P, 1442 more genes
nsv3917652	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 20,249,886-36,169,075 , GRCh38 chr15: 23,319,714-38,089,582 , GRCh37 chr15: 22,698,522-38,381,783	CHRM5, LOC105370764, 345 more genes
nsv4674936	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 22,770,421-36,861,479 , GRCh38.p12 chr15: 23,319,714-36,569,278	CHRM5, SNORD115-48, 330 more genes
nsv3921026	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 22,830,109-35,283,797 , GRCh38 chr15: 25,033,869-37,204,304 , GRCh37 chr15: 25,279,016-37,496,505	CHRM5, SNORD116-17, 303 more genes
nsv3915967	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr15: 32,635,803-40,233,825 , GRCh37 chr15: 32,928,004-40,526,026 , NCBI36 chr15: 30,715,296-38,313,318	CHRM5, ANP32AP1, 112 more genes
nsv3920384	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 30,405,629-37,473,561 , GRCh38 chr15: 32,326,136-39,394,068 , GRCh37 chr15: 32,618,337-39,686,269	CHRM5, PGBD4, 113 more genes
nsv6315190	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 33,809,650-40,027,263 , GRCh38.p12 chr15: 33,517,449-39,735,062	CHRM5, RYR3, 84 more genes
nsv4675391	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 34,197,488-38,656,254 , GRCh38.p12 chr15: 33,905,287-38,364,053	CHRM5, TPST2P1, 65 more genes
nsv4675702	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 31,675,452-35,689,958 , GRCh38.p12 chr15: 31,383,249-35,397,757 , GRCh38.p12 chr15\|NT_187660.1: 2,721,316-5,161,414	CHRM5, AVEN, 113 more genes
nsv3918749	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 29,304,042-32,054,898 , GRCh37.p13 chr15: 31,516,750-34,267,606 , GRCh38.p12 chr15: 31,224,547-33,975,405 , GRCh38.p12 chr15\|NT_187660.1: 2,721,316-5,161,414 , GRCh38.p12 chr15\|NW_011332701.1: 3,397,884-4,998,962	CHRM5, ULK4P1, 74 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	CHRM5, 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	CHRM5, 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	CHRM5, 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	CHRM5, 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	CHRM5, 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	CHRM5, RNU6-953P, 1385 more genes
nsv3912885	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr15: 23,319,714-38,545,325 , NCBI36 chr15: 20,316,992-36,624,818 , GRCh37 chr15: 22,765,628-38,837,526	CHRM5, LOC105370773, 350 more genes
nsv3921227	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 30,686,791-33,279,922 , GRCh37 chr15: 32,899,499-35,492,630 , GRCh38 chr15: 32,607,298-35,200,429	CHRM5, TMCO5B, 52 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 41

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Number of Variants: 20

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Supplemental Content

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