ClinVar for Gene (Select 101928455) - ClinVar - NCBI

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Links from Gene

Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 150244	GRCh38/hg38 2q22.2-22.3(chr2:143294079-147713830)x1	ARHGAP15, ARHGAP15-AS1 +43 more	Copy number loss	See cases	GPathogenic
Select item 149932	GRCh38/hg38 2q22.3(chr2:144213114-144668146)x1	GTDC1, LINC01412 +15 more	Copy number loss	See cases	GPathogenic
Select item 148432	GRCh38/hg38 2q22.1-22.3(chr2:136937358-146681810)x1	ARHGAP15, ARHGAP15-AS1 +75 more	Copy number loss	See cases	GPathogenic
Select item 146076	GRCh38/hg38 2q22.3-24.1(chr2:143900149-158321624)x3	ACVR1, ACVR1C +238 more	Copy number gain	See cases	GPathogenic
Select item 144170	GRCh38/hg38 2q22.3(chr2:144434699-146191493)x1	LINC01412, LINC01966 +15 more	Copy number loss	See cases	GPathogenic
Select item 60214	GRCh38/hg38 2q22.3(chr2:143988786-144558029)x1	GTDC1, LINC01412 +13 more	Copy number loss	See cases	GPathogenic
Select item 60212	GRCh38/hg38 2q22.2-22.3(chr2:141666537-147845662)x1	ACVR2A, ARHGAP15 +57 more	Copy number loss	See cases	GPathogenic
Select item 59149	GRCh38/hg38 2q22.3(chr2:144461848-144665266)x3	LINC01412, LINC02993 +3 more	Copy number gain	See cases	GPathogenic
Select item 57333	GRCh38/hg38 2q22.1-22.3(chr2:140186521-146528244)x1	ARHGAP15, ARHGAP15-AS1 +50 more	Copy number loss	See cases	GPathogenic
Select item 57256	GRCh38/hg38 2q22.3(chr2:144500115-144728038)x1	LINC01412, LINC02993 +4 more	Copy number loss	See cases	GPathogenic
Select item 34454	GRCh38/hg38 2q22.3(chr2:143900149-144668138)x3	GTDC1, LINC01412 +17 more	Copy number gain	See cases	GUncertain significance
Select item 4765	NC_000002.12:g.(144114719_144303837)_(144566562_144681958)del	GTDC1, LINC01412 +15 more	Deletion	Mowat-Wilson syndrome	GPathogenic