ythdc2[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
nsv3873267	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 112,903,834-112,945,992 , GRCh38.p12 chr5: 113,568,137-113,610,295	YTHDC2
nsv3878330	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 112,911,165-112,945,992 , GRCh38.p12 chr5: 113,575,468-113,610,295	YTHDC2
nsv3874547	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 112,916,780-112,945,992 , GRCh38.p12 chr5: 113,581,083-113,610,295	YTHDC2
nsv3887648	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 112,917,278-112,945,992 , GRCh38.p12 chr5: 113,581,581-113,610,295	YTHDC2
nsv3918420	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr5: 112,874,992-113,022,126 , GRCh37.p13 chr5: 112,847,093-112,994,227 , GRCh38.p12 chr5: 113,511,396-113,658,530	YTHDC2, LOC107986441
nsv3889848	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719	YTHDC2, MEGF10, 2080 more genes
nsv3884357	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 86,400,000-154,000,000 , GRCh38.p12 chr5: 87,104,183-154,620,440	YTHDC2, TXNDC15, 962 more genes
nsv3912937	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 105,955,289-155,551,397 , NCBI36 chr5: 105,983,188-155,483,975 , GRCh38 chr5: 106,619,588-156,124,387	YTHDC2, LINC01023, 783 more genes
nsv3915450	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 90,707,525-130,655,256 , NCBI36 chr5: 90,743,281-130,683,155 , GRCh38 chr5: 91,411,708-131,319,563	YTHDC2, MCTP1, 422 more genes
nsv3916468	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 89,670,423-127,412,115 , GRCh38 chr5: 90,374,606-128,076,423 , NCBI36 chr5: 89,706,179-127,440,014	YTHDC2, LOC105379149, 406 more genes
nsv3920768	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 92,235,441-118,949,814 , GRCh38 chr5: 92,899,734-119,614,119 , NCBI36 chr5: 92,261,197-118,977,713	YTHDC2, LOC102724720, 292 more genes
nsv3872414	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 100,607,918-125,900,735 , GRCh38.p12 chr5: 101,272,214-126,565,043	YTHDC2, ZRSR2P1, 248 more genes
nsv6313580	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 93,650,000-114,969,108 , GRCh38.p12 chr5: 94,314,295-115,633,411	YTHDC2, FER, 222 more genes
nsv3924205	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 110,023,143-129,439,531 , GRCh38 chr5: 110,687,442-130,103,838 , NCBI36 chr5: 110,051,042-129,467,430	YTHDC2, CSNK1G3, 231 more genes
nsv3923804	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 107,644,164-125,113,490 , NCBI36 chr5: 107,672,063-125,141,389 , GRCh38 chr5: 108,308,463-125,777,797	YTHDC2, FABP5P6, 202 more genes
nsv3910959	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 110,798,714-126,528,730 , NCBI36 chr5: 110,826,613-126,556,629 , GRCh38 chr5: 111,463,016-127,193,038	YTHDC2, LINC02208, 194 more genes
nsv6637111	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 112,557,391-128,106,299 , GRCh38.p12 chr5: 113,221,694-128,770,606	YTHDC2, SLC12A2, 180 more genes
nsv4456071	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 108,304,806-121,335,239 , GRCh38.p12 chr5: 108,969,105-121,999,544	YTHDC2, HMGN1P13, 153 more genes
nsv3874025	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 110,407,606-122,522,885 , GRCh38.p12 chr5: 111,071,908-123,187,191	YTHDC2, LINC02215, 155 more genes
nsv3919588	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 101,736,999-112,957,626 , GRCh37 chr5: 101,709,100-112,929,727 , GRCh38 chr5: 102,373,396-113,594,030	YTHDC2, CAMK4, 93 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 38

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

Recent activity