rps3[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
nsv3885403	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 100,022,125-100,035,230 , GRCh38.p12 chr6: 99,574,249-99,587,354	RPS3P5, TSTD3
nsv3921583	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr16: 76,944,540-77,483,227 , GRCh37 chr16: 78,387,039-78,925,726 , GRCh38 chr16: 78,353,142-78,891,829	RPS3P7, WWOX, 3 more genes
nsv3898427	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 78,854,228-79,136,139 , GRCh38.p12 chr16: 78,820,331-79,102,242	WWOX, LOC107984806, 1 more genes
nsv3880836	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 7,274,354-7,370,153 , GRCh38.p12 chr6: 7,274,121-7,369,920	SSR1, CAGE1, 2 more genes
nsv3913862	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 78,489,014-79,063,832 , GRCh38 chr16: 78,455,117-79,029,935 , NCBI36 chr16: 77,046,515-77,621,333	RPS3P7, WWOX, 2 more genes
nsv3912337	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr6: 7,047,409-7,324,024 , GRCh37.p13 chr6: 7,102,410-7,379,025 , GRCh38.p12 chr6: 7,102,177-7,378,792	CAGE1, RPS3P4, 3 more genes
nsv4457269	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 7,198,136-7,338,171 , GRCh38.p12 chr6: 7,197,903-7,337,938	RPS3P4, CAGE1, 2 more genes
nsv4683491	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 99,997,384-100,062,635 , GRCh38.p12 chr6: 99,549,508-99,614,759	RPS3P5, PRDM13, 2 more genes
nsv4683054	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 100,010,718-100,062,635 , GRCh38.p12 chr6: 99,562,842-99,614,759	PRDM13, RPS3P5, 2 more genes
nsv5380796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397	RPS3, FAUP4, 2031 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	LOC107986534, FYN, 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	RN7SL509P, LAMA4, 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	TUBE1, PLN, 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-AS1, SEC63, 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	RNA5SP211, RNU6-1106P, 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	LOC101927405, GPR6, 211 more genes
nsv3912723	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 30,288,202-45,731,170 , GRCh37.p13 chr20: 30,824,541-46,297,763 , GRCh38.p12 chr20: 32,236,738-47,669,019	LOC107985448, LOC105372613, 370 more genes
nsv3921095	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 69,005,977-83,499,227 , GRCh38 chr16: 70,414,573-84,908,120 , GRCh37 chr16: 70,448,476-84,941,726	NECAB2, CENPN-AS1, 219 more genes
nsv3921817	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 2,862,874-16,698,019 , GRCh38 chr6: 2,862,640-16,697,788 , NCBI36 chr6: 2,807,873-16,805,998	RN7SKP293, LOC105374906, 230 more genes
nsv3911792	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 101,974-13,964,135 , GRCh38 chr6: 156,974-13,855,925 , GRCh37 chr6: 156,974-13,856,156	SIRT5, PKMP5, 228 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 202

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Number of Variants: 20

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