"GeneDx"[submitter] AND "LMNB2"[gene] - ClinVar

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Search results

Items: 33

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59081	GRCh38/hg38 19p13.3(chr19:1565575-4108128)x3	ABHD17A, ADAT3 +362 more	Copy number gain	See cases	GPathogenic
Select item 59082	GRCh38/hg38 19p13.3-13.2(chr19:1972245-9648879)x3	LOC130063254, LOC130063255 +810 more	Copy number gain	See cases	GPathogenic
Select item 1245133	NM_032737.4(LMNB2):c.*272G>C	LMNB2	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1229867	NM_032737.4(LMNB2):c.1822-220C>T	LMNB2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1235386	NM_032737.4(LMNB2):c.1821+291C>T	LMNB2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1248663	NM_032737.4(LMNB2):c.1821+274A>C	LMNB2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1276055	NM_032737.4(LMNB2):c.1591-173C>T	LMNB2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1174345	NM_032737.4(LMNB2):c.1590+237G>A	LMNB2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1248243	NM_032737.4(LMNB2):c.1590+71A>G	LMNB2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 475776	NM_032737.4(LMNB2):c.1554G>C (p.Thr518=)	LMNB2	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 1279540	NM_032737.4(LMNB2):c.1483-34T>C	LMNB2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1288914	NM_032737.4(LMNB2):c.1483-182A>G	LMNB2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1273813	NM_032737.4(LMNB2):c.1483-260G>A	LMNB2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 129488	NM_032737.4(LMNB2):c.1416T>C (p.Gly472=)	LMNB2	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 1284131	NM_032737.4(LMNB2):c.1202+48A>G	LMNB2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1241642	NM_032737.4(LMNB2):c.982-38T>C	LMNB2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1267290	NM_032737.4(LMNB2):c.856-30G>A	LMNB2, MIR7108	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 1287600	NM_032737.4(LMNB2):c.685-165C>T	LMNB2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1221219	NM_032737.4(LMNB2):c.685-287A>G	LMNB2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1288705	NM_032737.4(LMNB2):c.684+163G>A	LMNB2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1277996	NM_032737.4(LMNB2):c.684+42G>A	LMNB2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1244022	NM_032737.4(LMNB2):c.402-136G>A	LMNB2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1179296	NM_032737.4(LMNB2):c.402-149G>T	LMNB2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1274497	NM_032737.4(LMNB2):c.402-262G>C	LMNB2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1241543	NM_032737.4(LMNB2):c.402-272A>G	LMNB2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1228861	NM_032737.4(LMNB2):c.401+39T>C	LMNB2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1182410	NM_032737.4(LMNB2):c.265-27G>A	LMNB2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1251087	NM_032737.4(LMNB2):c.265-70C>T	LMNB2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1272536	NM_032737.4(LMNB2):c.265-224C>T	LMNB2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1257297	NM_032737.4(LMNB2):c.265-295G>A	LMNB2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1254069	NM_032737.4(LMNB2):c.264+260G>T	LOC130063064, LMNB2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 253917	GRCh37/hg19 19p13.3(chr19:1952590-2698712)x3	GADD45B, BTBD2 +19 more	Copy number gain	See cases	GUncertain significance
Select item 253623	GRCh37/hg19 19p13.3(chr19:277373-2555164)x3	ABCA7, ABHD17A +87 more	Copy number gain	See cases	GPathogenic

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Items: 33