faxc[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
nsv3880626	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 85,988,428-120,548,687 , GRCh38.p12 chr6: 85,278,710-120,227,541	FAXC, LOC107986534, 426 more genes
nsv6313858	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 92,054,891-118,329,651 , GRCh38.p12 chr6: 91,345,173-118,008,488	FAXC, RN7SL509P, 311 more genes
nsv3924576	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 97,164,591-122,524,393 , GRCh38 chr6: 96,609,994-122,161,548 , GRCh37 chr6: 97,057,870-122,482,694	FAXC, TUBE1, 318 more genes
nsv3876958	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 95,549,951-116,684,929 , GRCh38.p12 chr6: 94,840,233-116,363,766	FAXC, LIN28B-AS1, 258 more genes
nsv3877239	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 94,202,605-109,878,834 , GRCh38.p12 chr6: 93,492,887-109,557,631	FAXC, RNA5SP211, 155 more genes
nsv4768376	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 98,949,950-114,533,905 , GRCh38.p12 chr6: 98,502,074-114,212,741	FAXC, LOC101927405, 211 more genes
nsv3874571	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 97,384,446-110,247,755 , GRCh38.p12 chr6: 96,936,570-109,926,552	FAXC, NPM1P38, 130 more genes
nsv3879439	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 92,576,950-104,658,245 , GRCh38.p12 chr6: 91,867,232-104,210,370	FAXC, FBXL4, 75 more genes
nsv6636338	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 96,946,110-106,497,526 , GRCh38.p12 chr6: 96,498,234-106,049,651	FAXC, BVES-AS1, 74 more genes
nsv6636533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 96,596,732-105,554,568 , GRCh38.p12 chr6: 96,148,856-105,106,693	FAXC, MCHR2-AS1, 65 more genes
nsv3914907	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 98,408,373-103,135,165 , GRCh38 chr6: 97,853,776-102,580,597 , GRCh37 chr6: 98,301,652-103,028,472	FAXC, BDH2P1, 33 more genes
nsv3921137	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 99,116,405-101,714,826 , GRCh38 chr6: 98,668,529-101,266,950 , NCBI36 chr6: 99,223,126-101,821,547	FAXC, MIR548AI, 25 more genes
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	FAXC, LOC105378061, 2914 more genes
nsv3879811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083	FAXC, RNU6-411P, 2910 more genes
nsv3887898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394	FAXC, SOD1P1, 2905 more genes
nsv3889814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382	FAXC, ITPR3, 2905 more genes
nsv3919111	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 74,382,807-142,040,500 , NCBI36 chr6: 75,149,243-142,403,330 , GRCh37 chr6: 75,092,523-142,361,637	FAXC, RNU6-770P, 810 more genes
nsv6636789	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 97,904,220-99,964,434 , GRCh38.p12 chr6: 97,456,344-99,516,558	FAXC, POU3F2, 15 more genes
nsv4675136	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 98,870,687-100,270,433 , GRCh38.p12 chr6: 98,422,811-99,822,557	FAXC, CCNC, 13 more genes
nsv3921775	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr6: 97,691,375-103,286,627 , GRCh37.p13 chr6: 97,584,654-103,179,934 , GRCh38.p12 chr6: 97,136,778-102,732,059	FAXC, CCNC, 38 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

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Search details

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