card18[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
nsv5380796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397	CARD18, FAUP4, 2031 more genes
nsv3904761	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 80,053,454-113,316,236 , GRCh38.p12 chr11: 80,342,410-113,445,514	CARD18, RPS6P16, 449 more genes
nsv3913977	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 77,943,882-106,650,146 , GRCh38 chr11: 78,232,836-106,779,420 , NCBI36 chr11: 77,621,530-106,155,356	CARD18, PLS1P1, 349 more genes
nsv3910101	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 87,796,211-113,996,548 , GRCh37.p13 chr11: 88,156,563-114,491,338 , GRCh38.p12 chr11: 88,423,395-114,620,616	CARD18, PHB1P16, 385 more genes
nsv3894488	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 88,152,458-109,414,650 , GRCh38.p12 chr11: 88,419,290-109,543,924	CARD18, RNU6-16P, 270 more genes
nsv3910663	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 91,086,659-109,595,582 , NCBI36 chr11: 90,459,475-108,971,518 , GRCh37 chr11: 90,819,827-109,466,308	CARD18, LOC101060084, 230 more genes
nsv5672640	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976	CARD18, HSPD1P13, 239 more genes
nsv4455554	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 104,101,411-116,680,918 , GRCh38.p12 chr11: 104,230,683-116,810,202	CARD18, LINC02732, 198 more genes
nsv4675680	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 103,320,065-114,349,787 , GRCh38.p12 chr11: 103,449,337-114,479,065	CARD18, DRD2, 181 more genes
nsv6637687	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 101,371,503-109,306,519 , GRCh38.p12 chr11: 101,500,772-109,435,793	CARD18, GRIA4, 111 more genes
nsv3924464	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 97,733,839-105,435,083 , GRCh38 chr11: 98,357,901-106,059,146 , GRCh37 chr11: 98,228,629-105,929,873	CARD18, ARHGAP42, 91 more genes
nsv3912128	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 104,510,196-105,323,725 , GRCh37 chr11: 104,380,924-105,194,452 , NCBI36 chr11: 103,886,134-104,699,662	CARD18, CARD17P, 16 more genes
nsv3893233	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576	CARD18, LOC105376598, 2842 more genes
nsv3900144	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169	CARD18, RTN3, 2833 more genes
nsv3908873	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576	CARD18, IGHMBP2, 2829 more genes
nsv6315537	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576	CARD18, PYGM, 2125 more genes
nsv3898361	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 71,588,805-116,680,918 , GRCh38.p12 chr11: 71,877,759-116,810,202	CARD18, SESN3, 694 more genes
nsv3922253	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 100,219,331-134,910,140 , NCBI36 chr11: 99,724,541-134,415,350 , GRCh38 chr11: 100,348,599-135,040,246	CARD18, RPS27P19, 655 more genes
nsv6289927	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 104,288,964-134,937,416 , GRCh38.p12 chr11: 104,418,236-135,067,522	CARD18, IGSF9B, 592 more genes
nsv3922086	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 104,142,626-107,019,997 , NCBI36 chr11: 103,518,564-106,395,933 , GRCh37 chr11: 104,013,354-106,890,723	CARD18, LOC105369468, 36 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 30

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Number of Variants: 20

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Supplemental Content

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Search details

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