fam81b[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
nsv4729036	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 94,781,047-94,875,584 , GRCh38.p12 chr5: 95,445,343-95,539,880	FAM81B, SKIC3, 1 more genes
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	FAM81B, 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	FAM81B, 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	FAM81B, 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	FAM81B, 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	FAM81B, 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	FAM81B, 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	FAM81B, 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	FAM81B, 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	FAM81B, 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	FAM81B, 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	FAM81B, LOC105379090, 142 more genes
nsv3874231	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 87,512,314-95,096,562 , GRCh38.p12 chr5: 88,216,497-95,760,858	FAM81B, ARRDC3, 71 more genes
nsv3912526	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 91,386,552-98,365,880 , NCBI36 chr5: 90,718,125-97,729,488 , GRCh37 chr5: 90,682,369-97,701,584	FAM81B, RTRAFP2, 77 more genes
nsv4457026	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 92,386,982-94,865,113 , GRCh38.p12 chr5: 93,051,276-95,529,409	FAM81B, POLD2P1, 21 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	FAM81B, 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	FAM81B, 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	FAM81B, 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	FAM81B, 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	FAM81B, CSNK1A1P3, 413 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 32

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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