znf229[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 14

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Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3896228	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 44,896,740-44,938,688 , GRCh38.p12 chr19: 44,392,576-44,434,513	ZNF229, ZNF285
nsv3902184	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 44,901,526-44,935,485 , GRCh38.p12 chr19: 44,397,361-44,431,310	ZNF229, ZNF285
nsv3904145	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 44,858,873-44,934,653 , GRCh38.p12 chr19: 44,354,721-44,430,478	ZNF229, ZNF285, 1 more genes
nsv3891669	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 43,013,365-47,241,534 , GRCh38.p12 chr19: 42,509,213-46,738,277	ZNF229, MIR320E, 189 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	ZNF229, 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	ZNF229, 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	ZNF229, 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	ZNF229, BCKDHA, 1102 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	ZNF229, ZNF461, 735 more genes
nsv4676357	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308	ZNF229, MIR4324, 485 more genes
nsv3890841	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 44,300,416-45,639,540 , GRCh38.p12 chr19: 43,796,264-45,136,282	ZNF229, ZNF225, 57 more genes
nsv1398140	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 44,466,919-45,029,206 , GRCh38.p12 chr19: 43,962,767-44,525,173	ZNF229, CEACAM20, 23 more genes
nsv7095657	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 44,011,002-45,213,778 , GRCh38.p12 chr19: 43,506,850-44,710,506	ZNF229, RN7SL368P, 52 more genes
nsv4436634	complex substitution	1	nstd102	human	Uncertain significance	GRCh38.p12 chr19: 43,997,366-44,819,487 , GRCh37 chr19: 44,501,518-45,322,744	ZNF229, BCL3, 34 more genes

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znf229[All Fields] AND 1[has_clinical] (15)
dbVar
Human respiratory syncytial virus strain RSVA/human/USA/A1997-12-35/1997, comple...
Human respiratory syncytial virus strain RSVA/human/USA/A1997-12-35/1997, complete genome
gi|392976429|gb|JX069800.1|

Nucleotide
CG31955 uncharacterized protein [Drosophila melanogaster]
CG31955 uncharacterized protein [Drosophila melanogaster]
Gene ID:319045

Gene

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