FILNC1[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 150937	GRCh38/hg38 6q13-24.1(chr6:74382807-142040500)x3	LOC129996876, LOC129996877 +1449 more	Copy number gain	See cases	GPathogenic
Select item 155377	GRCh38/hg38 6q23.2-27(chr6:133537271-165875545)x3	LOC129997450, LOC129997451 +1002 more	Copy number gain	See cases	GPathogenic
Select item 1684644	Single allele	ABRACL, AHI1 +260 more	Deletion	Autoinflammatory syndrome, familial, Behcet-like	GPathogenic
Select item 147665	GRCh38/hg38 6q23.3-25.3(chr6:135358150-155455117)x3	LOC129389692, LOC129389693 +614 more	Copy number gain	See cases	GPathogenic
Select item 148927	GRCh38/hg38 6q24.1(chr6:139002616-140199336)x3	ABRACL, CITED2 +42 more	Copy number gain	See cases	GUncertain significance
Select item 155708	GRCh38/hg38 6q24.1(chr6:139397617-139932971)x3	FILNC1, LINC01625 +11 more	Copy number gain	See cases	GUncertain significance
Select item 148816	GRCh38/hg38 6q24.1(chr6:139455977-140318558)x3	FILNC1, LINC01625 +14 more	Copy number gain	See cases	GLikely benign

ClinVar