cep89[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
nsv3897847	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 33,370,711-33,371,145 , GRCh38.p12 chr19: 32,879,805-32,880,239	CEP89
nsv6310476	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 33,439,152-33,439,294 , GRCh38.p12 chr19: 32,948,246-32,948,388	CEP89
nsv7095275	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 33,439,152-33,457,392 , GRCh38.p12 chr19: 32,948,246-32,966,486	CEP89, RPL31P60
nsv7095200	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 33,457,246-33,464,488 , GRCh38.p12 chr19: 32,966,340-32,973,582	CEP89, FAAP24
nsv3883378	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr19: 33,321,553-33,390,958 , GRCh38 chr19: 32,830,647-32,900,052	CEP89, SLC7A9, 1 more genes
nsv3891724	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr19: 33,321,553-33,390,899 , GRCh38.p12 chr19: 32,830,647-32,899,993	CEP89, SLC7A9, 1 more genes
nsv6637511	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 33,319,212-33,395,193 , GRCh38.p12 chr19: 32,828,306-32,904,287	CEP89, TDRD12, 2 more genes
nsv3919296	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 34,844,605-43,297,203 , GRCh37 chr19: 30,152,765-38,605,363 , GRCh38 chr19: 29,661,858-38,114,723	CEP89, UBA2, 241 more genes
nsv3916007	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 30,162,231-38,393,630 , NCBI36 chr19: 34,854,071-43,085,470 , GRCh38 chr19: 29,671,324-37,902,990	CEP89, MAG, 238 more genes
nsv3918197	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 31,367,353-35,417,098 , NCBI36 chr19: 36,550,099-40,599,840 , GRCh37 chr19: 31,858,259-35,908,000	CEP89, LINC01531, 110 more genes
nsv3904885	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923	CEP89, ZNF321P, 2443 more genes
nsv3903203	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793	CEP89, BABAM1, 2426 more genes
nsv3903092	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521	CEP89, LENG8, 2408 more genes
nsv3913730	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354	CEP89, BCKDHA, 1102 more genes
nsv6290300	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324	CEP89, ZNF420, 574 more genes
nsv4457372	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575	CEP89, ZNF461, 735 more genes
nsv3914228	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 17,148,576-40,106,894 , GRCh38 chr19: 17,176,767-34,924,150 , GRCh37 chr19: 17,287,576-35,415,054	CEP89, LOC105372355, 411 more genes
nsv3900139	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 30,735,448-36,120,396 , GRCh38.p12 chr19: 30,244,541-35,629,494	CEP89, ZNF599, 130 more genes
nsv3919618	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr19: 32,962,986-39,966,686 , GRCh38 chr19: 27,780,238-34,783,942 , GRCh37 chr19: 28,271,146-35,274,846	CEP89, LINC00906, 112 more genes
nsv7095478	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 33,167,170-36,643,309 , GRCh38.p12 chr19: 32,676,264-36,152,407	CEP89, NFKBID, 141 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 21

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Number of Variants: 20

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