TGFB2-AS1[gene] - ClinVar

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Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58112	GRCh38/hg38 1q31.1-42.11(chr1:187143981-224299417)x3	LOC129932539, LOC129932540 +1148 more	Copy number gain	See cases	GPathogenic
Select item 153790	GRCh38/hg38 1q32.1-42.12(chr1:204764914-225408698)x3	LOC129388734, LOC129388735 +723 more	Copy number gain	See cases	GPathogenic
Select item 155660	GRCh38/hg38 1q32.2-44(chr1:207346642-248930485)x3	ABCB10, ACBD3 +1428 more	Copy number gain	See cases	GPathogenic
Select item 1809607	GRCh38/hg38 1q32.2-42.13(chr1:228006998-228061271)x2	LOC126806029, LOC129932471 +720 more	Copy number loss	Orofacial cleft 2	Gassociation
Select item 58116	GRCh38/hg38 1q32.2-44(chr1:209646207-248931113)x3	LOC120908923, LOC120947224 +1352 more	Copy number gain	See cases	GPathogenic
Select item 145652	GRCh38/hg38 1q32.2-44(chr1:209963625-248918469)x3	ABCB10, ACBD3 +1326 more	Copy number gain	See cases	GPathogenic
Select item 57302	GRCh38/hg38 1q32.3-44(chr1:214023812-248918469)x3	LOC129932855, LOC129932856 +1168 more	Copy number gain	See cases	GPathogenic
Select item 161040	GRCh38/hg38 1q41(chr1:215206760-222004068)x1	BPNT1, C1orf115 +138 more	Copy number loss	See cases	GPathogenic
Select item 34890	GRCh38/hg38 1q41(chr1:215206760-222004068)x1	BPNT1, C1orf115 +138 more	Copy number loss	See cases	GPathogenic
Select item 58129	GRCh38/hg38 1q41(chr1:215447347-221971832)x3	BPNT1, C1orf115 +135 more	Copy number gain	See cases	GPathogenic
Select item 438260	Single allele	BPNT1, C1orf115 +146 more	Deletion	Usher syndrome	GLikely pathogenic
Select item 60081	GRCh38/hg38 1q41(chr1:216518607-219827290)x1	ESRRG, GPATCH2 +55 more	Copy number loss	See cases	GPathogenic
Select item 60082	GRCh38/hg38 1q41(chr1:217452423-218818361)x1	GPATCH2, LINC00210 +22 more	Copy number loss	See cases	GPathogenic
Select item 154219	GRCh38/hg38 1q41(chr1:217558925-218732002)x3	GPATCH2, LINC00210 +19 more	Copy number gain	See cases	GUncertain significance
Select item 57198	GRCh38/hg38 1q41(chr1:218321722-218961624)x1	LINC01710, LINC02869 +9 more	Copy number loss	See cases	GUncertain significance
Select item 1249061	NC_000001.11:g.218345083CTTC[1]	TGFB2, TGFB2-AS1	Microsatellite	not provided	GBenign
Select item 1241729	NC_000001.11:g.218345173A>C	TGFB2, TGFB2-AS1	Single nucleotide variant	not provided	GBenign
Select item 295455	NM_003238.6(TGFB2):c.-1302A>G	TGFB2, TGFB2-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 295456	NM_003238.6(TGFB2):c.-1278AAGAGA[3]	TGFB2, TGFB2-AS1	Microsatellite (5 prime UTR variant +1 more)	Loeys-Dietz syndrome 4 +1 more	GUncertain significance
Select item 295457	NM_003238.6(TGFB2):c.-1271A>G	TGFB2, TGFB2-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	Loeys-Dietz syndrome 4	GUncertain significance
Select item 875513	NM_003238.6(TGFB2):c.-1249G>A	TGFB2, TGFB2-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	Loeys-Dietz syndrome 4	GUncertain significance
Select item 875514	NM_003238.6(TGFB2):c.-1237G>C	TGFB2, TGFB2-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	Loeys-Dietz syndrome 4	GUncertain significance
Select item 675714	NM_003238.6(TGFB2):c.-1230G>A	TGFB2, TGFB2-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	Loeys-Dietz syndrome 4 +1 more	GBenign/Likely benign
Select item 295458	NM_003238.6(TGFB2):c.-1153G>T	TGFB2, TGFB2-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	Loeys-Dietz syndrome 4	GUncertain significance

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Items: 24