prep[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
nsv7093713	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 3,180,223-3,214,971 , GRCh38.p12 chr10: 3,138,031-3,172,779	PITRM1-AS1, PITRM1
nsv3923107	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 3,148,116-3,202,491 , GRCh38 chr10: 3,105,924-3,160,299	PITRM1, SNORD142, 2 more genes
nsv4456319	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 3,173,336-3,232,117 , GRCh38.p12 chr10: 3,131,144-3,189,925	SNORD142, PITRM1, 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	PREP, 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	PREP, 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	PREP, 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	PREP, 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	PREP, LINC02518, 266 more genes
nsv3914771	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 54,086-19,336,980 , NCBI36 chr10: 90,026-19,665,915 , GRCh37 chr10: 100,026-19,625,909	COX6CP17, TUBAL3, 302 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	PREP, 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	PREP, LOC101927405, 211 more genes
nsv3918372	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 70,478-13,736,564 , GRCh37 chr10: 224,406-13,778,564 , NCBI36 chr10: 106,418-13,818,570	IL9RP2, PRKCQ, 232 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	PREP, NPM1P38, 130 more genes
nsv3890577	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 100,026-12,842,179 , GRCh38.p12 chr10: 54,086-12,800,180	LOC105376364, LOC101930421, 208 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	PREP, 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	PREP, BVES-AS1, 74 more genes
nsv3893746	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 136,361-8,850,609 , GRCh38.p12 chr10: 90,421-8,808,646	TRV-TAC3-1, IL15RA, 163 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	PREP, RPS19P5, 121 more genes
nsv5672604	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 120,001-6,920,000 , GRCh38.p12 chr10: 74,061-6,878,038	PITRM1-AS1, TRV-TAC3-1, 133 more genes
nsv3924022	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 105,200-6,291,337 , GRCh38 chr10: 69,260-6,209,368 , GRCh37 chr10: 224,406-6,251,331	LINC02561, AKR1C1, 120 more genes

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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 71

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Number of Variants: 20

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