"ISCA site 1"[submitter] AND "TMEM132D"[gene] - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 155589	GRCh38/hg38 12q24.21-24.33(chr12:114268403-133201316)x3	ANKLE2, ARL6IP4 +906 more	Copy number gain	See cases	GPathogenic
Select item 148578	GRCh38/hg38 12q24.31-24.33(chr12:120697672-133202490)x3	AACS, ABCB9 +663 more	Copy number gain	See cases	GPathogenic
Select item 146222	GRCh38/hg38 12q24.31-24.33(chr12:123509825-133191400)x3	LOC130009168, LOC130009169 +408 more	Copy number gain	See cases	GPathogenic
Select item 147998	GRCh38/hg38 12q24.32-24.33(chr12:127900499-129778294)x3	GLT1D1, LINC00507 +43 more	Copy number gain	See cases	GUncertain significance
Select item 151149	GRCh38/hg38 12q24.32-24.33(chr12:128487318-129325819)x3	GLT1D1, LOC100128276 +30 more	Copy number gain	See cases	GUncertain significance
Select item 150016	GRCh38/hg38 12q24.32-24.33(chr12:128510404-129187569)x4	GLT1D1, LOC100128276 +28 more	Copy number gain	See cases	GUncertain significance
Select item 153212	GRCh38/hg38 12q24.33(chr12:129318948-130000929)x3	LOC126861687, LOC126861688 +5 more	Copy number gain	See cases	GUncertain significance
Select item 32384	GRCh38/hg38 12q24.33(chr12:129325762-129943507)x3	LOC126861687, LOC126861688 +4 more	Copy number gain	See cases	GUncertain significance
Select item 148025	GRCh38/hg38 12q24.33(chr12:129475355-129675925)x1	LOC126861687, TMEM132D	Copy number loss	See cases	GUncertain significance
Select item 441984	GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)	HMGA2, HNF1A +1006 more	Copy number gain	See cases	GPathogenic
Select item 441983	GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)x3	A2M, A2ML1 +1006 more	Copy number gain	See cases	GPathogenic