Related gene-specific medical variations for Gene (Select 441234) - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 814976	GRCh37/hg19 7p11.2(chr7:57252805-57923840)x3	ZNF716	Copy number gain	not provided	GLikely benign
Select item 563377	GRCh37/hg19 7p11.2-11.1(chr7:57261122-58025410)x3	ZNF716	Copy number gain	not provided	GLikely benign
Select item 443818	GRCh37/hg19 7p11.2(chr7:57261122-57950667)x3	ZNF716	Copy number gain	See cases	GUncertain significance
Select item 443029	GRCh37/hg19 7p11.2-11.1(chr7:57524118-58025410)x3	ZNF716	Copy number gain	See cases	GLikely benign
Select item 442862	GRCh37/hg19 7p11.2(chr7:57252722-57919516)x3	ZNF716	Copy number gain	See cases	GUncertain significance
Select item 442679	GRCh37/hg19 7p11.2(chr7:57261122-57832850)x3	ZNF716	Copy number gain	See cases	GLikely benign
Select item 442308	GRCh37/hg19 7p11.2(chr7:57261122-57923504)x3	ZNF716	Copy number gain	See cases	GLikely benign
Select item 442065	GRCh37/hg19 7p11.2(chr7:57261122-57950845)x3	ZNF716	Copy number gain	See cases	GUncertain significance
Select item 442058	GRCh37/hg19 7p11.2(chr7:57261122-57919405)x3	ZNF716	Copy number gain	See cases	Gconflicting data from submitters
Select item 442053	GRCh37/hg19 7p11.2(chr7:57260919-57936172)x3	ZNF716	Copy number gain	See cases	GUncertain significance
Select item 442003	GRCh37/hg19 7p11.2(chr7:57261122-57914510)x3	ZNF716	Copy number gain	See cases	GUncertain significance
Select item 441688	GRCh37/hg19 7p11.2(chr7:57261122-57914385)x3	ZNF716	Copy number gain	See cases	GUncertain significance
Select item 441678	GRCh37/hg19 7p11.2(chr7:57261122-57861682)x3	ZNF716	Copy number gain	See cases	GUncertain significance
Select item 441578	GRCh37/hg19 7p11.2(chr7:57252722-57914510)x3	ZNF716	Copy number gain	See cases	GUncertain significance
Select item 223124	NC_000007.13:g.(?_57260919)_(57882330_?)dup	ZNF716	Duplication	Autism spectrum disorder	GUncertain significance
Select item 221825	GRCh37/hg19 7p11.2(chr7:57481104-57621951)x3	ZNF716	Copy number gain	Premature ovarian failure	GBenign
Select item 157054	Single allele	ZNF716	Duplication	Preeclampsia	Gnot provided