LINC02987[gene] - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 144406	GRCh38/hg38 19p13.2-q13.31(chr19:11227942-44626354)x3	ABHD8, ACP5 +2135 more	Copy number gain	See cases	GPathogenic
Select item 59114	GRCh38/hg38 19p13.12-q11(chr19:13974677-27839676)x3	ABHD8, ADGRE2 +695 more	Copy number gain	See cases	GPathogenic
Select item 57042	GRCh38/hg38 19p13.11-q13.11(chr19:17176767-34924150)x3	LOC130064154, LOC130064155 +625 more	Copy number gain	See cases	GPathogenic
Select item 148736	GRCh38/hg38 19q11(chr19:27362299-27992601)x3	ERVK-19, LINC00662 +2 more	Copy number gain	See cases	GLikely benign
Select item 148322	GRCh38/hg38 19q11-12(chr19:27362299-28388381)x4	ERVK-19, LINC00662 +8 more	Copy number gain	See cases	GLikely benign
Select item 148321	GRCh38/hg38 19q11-12(chr19:27362299-28388381)x3	ERVK-19, LINC00662 +8 more	Copy number gain	See cases	GLikely benign
Select item 146537	GRCh38/hg38 19q11-12(chr19:27362299-28373339)x3	ERVK-19, LINC00662 +6 more	Copy number gain	See cases	GUncertain significance
Select item 146328	GRCh38/hg38 19q11-12(chr19:27362299-28249987)x4	ERVK-19, LINC00662 +5 more	Copy number gain	See cases	GLikely benign
Select item 145666	GRCh38/hg38 19q11(chr19:27362299-27940935)x4	ERVK-19, LINC00662 +2 more	Copy number gain	See cases	GUncertain significance
Select item 60275	GRCh38/hg38 19q11-12(chr19:27362299-28173816)x3	ERVK-19, LINC00662 +5 more	Copy number gain	See cases	GUncertain significance
Select item 154980	GRCh38/hg38 19q11-12(chr19:27362301-28373332)x3	ERVK-19, LINC00662 +6 more	Copy number gain	See cases	GLikely benign
Select item 154866	GRCh38/hg38 19q11(chr19:27362301-27992620)x3	ERVK-19, LINC00662 +2 more	Copy number gain	See cases	GLikely benign
Select item 155638	GRCh38/hg38 19q11-13.11(chr19:27780238-34783942)x3	ANKRD27, C19orf12 +210 more	Copy number gain	See cases	GUncertain significance
Select item 145259	GRCh38/hg38 19q11(chr19:27781589-27992542)x3	LINC00662, LINC02987 +1 more	Copy number gain	See cases	GBenign
Select item 151465	GRCh38/hg38 19q11(chr19:27799110-27839617)x3	LINC02987	Copy number gain	See cases	GBenign
Select item 154766	GRCh38/hg38 19q11(chr19:27806964-27827471)x1	LINC02987	Copy number loss	See cases	GLikely benign
Select item 151455	GRCh38/hg38 19q11(chr19:27917896-28021290)x4	LINC02987	Copy number gain	See cases	GBenign