ClinVar for Gene (Select 129935618) - ClinVar - NCBI

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Links from Gene

Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 334386	NM_025216.2(WNT10A):c.-249G>C	LOC129935618, WNT10A	Single nucleotide variant (genic upstream transcript variant)	SchC6pf-Schulz-Passarge syndrome +3 more	GUncertain significance
Select item 334385	NM_025216.2(WNT10A):c.-270G>C	LOC129935618, WNT10A	Single nucleotide variant (genic upstream transcript variant)	SchC6pf-Schulz-Passarge syndrome +2 more	GUncertain significance
Select item 334384	NM_025216.2(WNT10A):c.-285C>T	LOC129935618, WNT10A	Single nucleotide variant (genic upstream transcript variant)	SchC6pf-Schulz-Passarge syndrome +2 more	GUncertain significance
Select item 334383	NM_025216.2(WNT10A):c.-312C>T	LOC129935618, WNT10A	Single nucleotide variant (genic upstream transcript variant)	SchC6pf-Schulz-Passarge syndrome +2 more	GLikely benign
Select item 334382	NM_025216.2(WNT10A):c.-341A>G	LOC129935618, WNT10A	Single nucleotide variant (genic upstream transcript variant)	SchC6pf-Schulz-Passarge syndrome +2 more	GUncertain significance
Select item 334381	NM_025216.2(WNT10A):c.-358G>A	LOC129935618, WNT10A	Single nucleotide variant (genic upstream transcript variant)	SchC6pf-Schulz-Passarge syndrome +2 more	GUncertain significance
Select item 334380	NM_025216.2(WNT10A):c.-370C>A	LOC129935618, WNT10A	Single nucleotide variant (genic upstream transcript variant)	SchC6pf-Schulz-Passarge syndrome +2 more	GUncertain significance
Select item 334379	NM_025216.2(WNT10A):c.-400T>G	LOC129935618, WNT10A	Single nucleotide variant (genic upstream transcript variant)	SchC6pf-Schulz-Passarge syndrome +2 more	GLikely benign
Select item 334378	NM_025216.2(WNT10A):c.-433C>G	LOC129935618, WNT10A	Single nucleotide variant (genic upstream transcript variant)	SchC6pf-Schulz-Passarge syndrome +2 more	GUncertain significance
Select item 155149	GRCh38/hg38 2q35-37.3(chr2:218101759-242126245)x3	LOC110120629, LOC110120691 +986 more	Copy number gain	See cases	GPathogenic
Select item 154206	GRCh38/hg38 2q32.2-37.3(chr2:189436149-241841232)x3	AAMP, ABCA12 +1687 more	Copy number gain	See cases	GPathogenic
Select item 150620	GRCh38/hg38 2q31.3-36.2(chr2:180513793-224302848)x3	INPP1, ITGA4 +1097 more	Copy number gain	See cases	GPathogenic
Select item 146683	GRCh38/hg38 2q34-37.3(chr2:210579676-242126245)x3	AAMP, ABCA12 +1148 more	Copy number gain	See cases	GPathogenic
Select item 59159	GRCh38/hg38 2q32.2-37.3(chr2:190310736-241892770)x3	LOC129935726, LOC129935727 +1665 more	Copy number gain	See cases	GPathogenic
Select item 59158	GRCh38/hg38 2q32.2-37.3(chr2:188818195-242065208)x3	LOC129935343, LOC129935344 +1703 more	Copy number gain	See cases	GPathogenic
Select item 57419	GRCh38/hg38 2q32.3-37.3(chr2:194898783-236473913)x3	LOC129935713, LOC129935714 +1299 more	Copy number gain	See cases	GPathogenic