znf569[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 18

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Number of Variants: 18

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3894316	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr19: 37,772,899-37,923,531 , GRCh38.p12 chr19: 37,281,997-37,432,629	ZNF569, ZNF527, 1 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	ZNF569, 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	ZNF569, MAG, 238 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	ZNF569, 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	ZNF569, 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	ZNF569, 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	ZNF569, 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	ZNF569, 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	ZNF569, ZNF461, 735 more genes
nsv3912447	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 42,502,119-47,934,680 , GRCh37 chr19: 37,810,279-43,242,840 , GRCh38 chr19: 37,319,377-42,738,688	ZNF569, MIR8077, 233 more genes
nsv3895066	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 37,582,250-41,630,908 , GRCh38.p12 chr19: 37,091,348-41,125,003	ZNF569, RNU6-140P, 162 more genes
nsv4676151	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr19: 37,820,245-38,150,396 , GRCh38.p12 chr19: 37,329,343-37,659,495	ZNF569, ZNF570, 11 more genes
nsv1398592	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 36,685,995-38,708,166 , GRCh38.p12 chr19: 36,195,093-38,217,526	ZNF569, ZNF607, 62 more genes
nsv3920617	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 37,598,298-38,170,622 , NCBI36 chr19: 42,290,138-42,862,462 , GRCh38 chr19: 37,107,396-37,679,721	ZNF569, ZNF570, 18 more genes
nsv4729776	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 37,820,377-38,083,967 , GRCh38.p12 chr19: 37,329,475-37,593,066	ZNF569, ZNF793-AS1, 10 more genes
nsv3909857	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 36,475,577-38,399,402 , GRCh38.p12 chr19: 35,984,675-37,908,762	ZNF569, ZNF790, 72 more genes
nsv6637740	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 37,389,799-38,562,489 , GRCh38.p12 chr19: 36,898,897-38,071,849	ZNF569, MTND5P45, 36 more genes
nsv4436633	complex substitution	1	nstd102	human	Uncertain significance	GRCh38.p12 chr19: 36,183,403-38,162,322 , GRCh37 chr19: 36,674,305-38,652,962	ZNF569, ZNF146, 60 more genes

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znf569[All Fields] AND 1[has_clinical] (19)
dbVar
MULTISPECIES: transcriptional regulator [Vibrio]
MULTISPECIES: transcriptional regulator [Vibrio]
gi|491539609|ref|WP_005397228.1|

Protein
Entomologisk Tidskrift[Journal] (1)
NLM Catalog
zinc finger protein Aiolos isoform 6 [Homo sapiens]
zinc finger protein Aiolos isoform 6 [Homo sapiens]
gi|38045967|ref|NP_899055.1|

Protein

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