st8sia4[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	ST8SIA4, 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	ST8SIA4, TXNDC15, 962 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	ST8SIA4, 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	ST8SIA4, 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	ST8SIA4, 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	ST8SIA4, LOC102724720, 292 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	ST8SIA4, 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	ST8SIA4, FBXL17, 204 more genes
nsv3914008	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 88,377,169-104,022,949 , NCBI36 chr5: 88,412,925-104,050,848 , GRCh38 chr5: 89,081,352-104,687,248	ST8SIA4, LOC105379080, 166 more genes
nsv3921368	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 86,672,700-100,860,147 , NCBI36 chr5: 86,708,456-100,888,046 , GRCh38 chr5: 87,376,883-101,524,443	ST8SIA4, LOC107986438, 158 more genes
nsv3879974	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 91,504,101-104,858,348 , GRCh38.p12 chr5: 92,208,284-105,522,647	ST8SIA4, LOC105379090, 142 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	ST8SIA4, 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	ST8SIA4, 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	ST8SIA4, SPEF2, 2490 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	ST8SIA4, 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	ST8SIA4, 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	ST8SIA4, MTATP6P2, 166 more genes
nsv3885295	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr5: 95,049,966-103,537,589 , GRCh38.p12 chr5: 95,714,262-104,201,888	ST8SIA4, CAST, 103 more genes
nsv4675472	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr5: 87,792,844-109,221,844 , GRCh38.p12 chr5: 88,497,027-109,886,143	ST8SIA4, CAST, 202 more genes
nsv3919762	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr5: 99,743,180-100,184,629 , GRCh37.p13 chr5: 99,715,281-100,156,730 , GRCh38.p12 chr5: 100,379,577-100,821,026	ST8SIA4, FAM174A, 4 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 26

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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