lin28b[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
nsv6313603	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 105,406,897-105,573,285 , GRCh38.p12 chr6: 104,959,022-105,125,410	LIN28B, RNU6-1106P, 1 more genes
nsv4456240	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 105,268,161-105,427,647 , GRCh38.p12 chr6: 104,820,286-104,979,772	LIN28B, HACE1, 2 more genes
nsv4455380	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 105,277,427-105,427,647 , GRCh38.p12 chr6: 104,829,552-104,979,772	LIN28B, LOC100422315, 2 more genes
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	LIN28B, 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	LIN28B, 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	LIN28B, 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	LIN28B, LIN28B-AS1, 258 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	LIN28B, LINC02518, 266 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	LIN28B, 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	LIN28B, 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	LIN28B, NPM1P38, 130 more genes
nsv3919897	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 103,834,033-114,362,096 , GRCh37 chr6: 103,727,340-114,255,403 , GRCh38 chr6: 103,279,465-113,934,239	LIN28B, HACE1, 174 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	LIN28B, 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	LIN28B, MCHR2-AS1, 65 more genes
nsv3913170	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 102,911,070-111,477,775 , GRCh38 chr6: 102,356,502-111,049,879 , GRCh37 chr6: 102,804,377-111,371,082	LIN28B, RPS19P5, 121 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	LIN28B, 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	LIN28B, 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	LIN28B, 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	LIN28B, 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	LIN28B, RNU6-770P, 810 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 22

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Number of Variants: 20

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Supplemental Content

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