ClinVar for Gene (Select 374987) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1707456	Single allele	ACADM, AK5 +188 more	Duplication	not specified	GUncertain significance
Select item 1233836	NM_144573.4(NEXN):c.-53+141G>T	LOC129930796, NEXN +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 1194335	NM_144573.4(NEXN):c.-53+36T>G	NEXN, NEXN-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 298084	NM_144573.3(NEXN):c.-212_-210GGC[7]	LOC129930795, NEXN +1 more	Microsatellite (non-coding transcript variant)	Dilated Cardiomyopathy, Dominant +2 more	GUncertain significance
Select item 152108	GRCh38/hg38 1p31.1(chr1:77777821-79122486)x1	ADGRL4, DNAJB4 +33 more	Copy number loss	See cases	GUncertain significance
Select item 150045	GRCh38/hg38 1p31.1-22.2(chr1:76419302-88628464)x1	ADGRL2, ADGRL4 +241 more	Copy number loss	See cases	GPathogenic
Select item 147765	GRCh38/hg38 1p32.1-22.3(chr1:58819605-86098611)x1	MIGA1, MIR101-1 +558 more	Copy number loss	See cases	GPathogenic
Select item 138513	NM_144573.4(NEXN):c.-58T>C	NEXN-AS1, NEXN	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GBenign

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