aqr[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
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	AQR, 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	AQR, 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	AQR, 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	AQR, 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	AQR, 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	AQR, 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	AQR, 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	AQR, RYR3, 84 more genes
nsv3919055	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 34,880,216-39,572,605 , NCBI36 chr15: 32,667,508-37,359,897 , GRCh38 chr15: 34,588,015-39,280,404	AQR, DPH6, 56 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	AQR, 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	AQR, AVEN, 113 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	AQR, 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	AQR, 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	AQR, 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	AQR, 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	AQR, 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	AQR, 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	AQR, 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	AQR, TMCO5B, 52 more genes
nsv4436396	complex substitution	1	nstd102	human	Pathogenic	GRCh38.p12 chr15: 34,346,036-41,764,885 , GRCh37 chr15: 34,638,237-42,057,083	AQR, ACTC1, 150 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 27

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Number of Variants: 20

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Supplemental Content

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Search details

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