efna5[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
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	EFNA5, 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	EFNA5, 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	EFNA5, 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	EFNA5, 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	EFNA5, LOC105379149, 406 more genes
nsv3924896	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 84,603,580-111,435,081 , GRCh37 chr5: 83,899,398-110,770,779 , NCBI36 chr5: 83,935,154-110,798,678	EFNA5, LOC107986438, 254 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	EFNA5, 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	EFNA5, 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	EFNA5, FER, 222 more genes
nsv3921006	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 92,554,566-112,651,391 , GRCh37 chr5: 92,528,810-112,623,492 , GRCh38 chr5: 93,193,104-113,287,795	EFNA5, FBXL17, 204 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	EFNA5, CAMK4, 93 more genes
nsv3920751	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 106,365,809-117,388,910 , GRCh37 chr5: 106,337,910-117,361,011 , GRCh38 chr5: 107,002,209-118,025,316	EFNA5, PSMC1P5, 125 more genes
nsv3923639	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 106,586,078-113,006,585 , NCBI36 chr5: 105,949,678-112,370,181 , GRCh37 chr5: 105,921,779-112,342,282	EFNA5, RACK1P1, 63 more genes
nsv3886374	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028	EFNA5, LOC105374618, 2499 more genes
nsv3871533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343	EFNA5, PCDHGC5, 2492 more genes
nsv3875235	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788	EFNA5, SPEF2, 2490 more genes
nsv3874238	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 106,716,357-180,687,338 , GRCh38.p12 chr5: 107,380,656-181,260,337	EFNA5, PJA2, 1228 more genes
nsv4455983	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 89,949,118-129,317,455 , GRCh38.p12 chr5: 90,653,301-129,981,762	EFNA5, LOC345576, 419 more genes
nsv3917856	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 74,163,186-110,809,453 , NCBI36 chr5: 73,494,767-110,173,052 , GRCh37 chr5: 73,459,011-110,145,153	EFNA5, CSNK1A1P3, 413 more genes
nsv3923731	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 96,454,445-114,050,905 , GRCh37 chr5: 95,790,149-113,386,602 , NCBI36 chr5: 95,815,905-113,414,501	EFNA5, MTATP6P2, 166 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 29

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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