fam184a[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	FAM184A, LOC107986534, 426 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	FAM184A, TUBE1, 318 more genes
nsv3920683	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 109,372,795-132,430,553 , GRCh37 chr6: 109,266,102-132,388,860 , GRCh38 chr6: 108,944,899-132,067,720	FAM184A, SSXP10, 298 more genes
nsv3910417	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 100,054,889-120,488,154 , NCBI36 chr6: 100,609,486-120,850,999 , GRCh37 chr6: 100,502,765-120,809,300	FAM184A, LINC02518, 266 more genes
nsv3924741	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 106,951,594-126,102,365 , GRCh38 chr6: 106,503,719-125,781,219 , NCBI36 chr6: 107,058,287-126,144,058	FAM184A, LOC105377979, 266 more genes
nsv6315321	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 115,941,808-133,892,653 , GRCh37.p13 chr6: 116,262,971-134,213,791	FAM184A, SLC18B1, 223 more genes
nsv7148249	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 113,857,248-130,442,177 , GRCh37.p13 chr6: 114,178,427-130,763,322	FAM184A, TRDN-AS1, 179 more genes
nsv3924661	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 115,601,230-128,514,324 , GRCh37 chr6: 115,922,394-128,835,469 , NCBI36 chr6: 116,029,087-128,877,162	FAM184A, MCM9, 146 more genes
nsv4457007	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 110,981,075-119,608,396 , GRCh38.p12 chr6: 110,659,872-119,287,231	FAM184A, HDAC2-AS2, 134 more genes
nsv3918326	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 116,145,074-123,993,898 , GRCh37.p13 chr6: 116,038,381-123,952,199 , GRCh38.p12 chr6: 115,717,217-123,631,054	FAM184A, MCM9, 93 more genes
nsv4768325	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 116,734,559-123,648,104 , GRCh38.p12 chr6: 116,413,396-123,326,959	FAM184A, GJA1, 80 more genes
nsv3914300	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 119,337,879-126,076,146 , GRCh38 chr6: 118,975,015-125,713,307 , GRCh37 chr6: 119,296,180-126,034,453	FAM184A, RNF217-AS1, 50 more genes
nsv1398200	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 116,681,080-119,775,014 , GRCh38.p12 chr6: 116,359,917-119,453,849	FAM184A, GPRC6A, 48 more genes
nsv1398489	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 117,810,940-119,417,749 , GRCh38.p12 chr6: 117,489,777-119,096,584	FAM184A, SLC35F1, 19 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	FAM184A, 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	FAM184A, 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	FAM184A, 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	FAM184A, 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	FAM184A, RNU6-770P, 810 more genes
nsv3924512	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 118,035,003-127,062,818 , GRCh37 chr6: 117,928,310-127,021,125 , GRCh38 chr6: 117,607,147-126,699,980	FAM184A, HSF2, 85 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 31

Page of 2

Number of Variants: 20

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Supplemental Content

Find related data

Search details

Recent activity