LINC01881[gene] - ClinVar

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Items: 34

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 146683	GRCh38/hg38 2q34-37.3(chr2:210579676-242126245)x3	AAMP, ABCA12 +1148 more	Copy number gain	See cases	GPathogenic
Select item 155149	GRCh38/hg38 2q35-37.3(chr2:218101759-242126245)x3	LOC110120629, LOC110120691 +986 more	Copy number gain	See cases	GPathogenic
Select item 161051	GRCh38/hg38 2q37.1-37.3(chr2:231770279-242126245)x1	LOC129935965, LOC129935966 +455 more	Copy number loss	See cases	GPathogenic
Select item 34724	GRCh38/hg38 2q37.1-37.3(chr2:231770279-242126245)x1	ACKR3, AGAP1 +455 more	Copy number loss	See cases	GPathogenic
Select item 58852	GRCh38/hg38 2q37.1-37.3(chr2:233453611-242099155)x1	RAB17-DT, RAMP1 +359 more	Copy number loss	See cases	GPathogenic
Select item 57457	GRCh38/hg38 2q37.1-37.3(chr2:234345842-242126245)x1	HDAC4, HDAC4-AS1 +334 more	Copy number loss	See cases	GPathogenic
Select item 58880	GRCh38/hg38 2q37.1-37.3(chr2:234668159-242126245)x1	PRLH, PRR21 +325 more	Copy number loss	See cases	GPathogenic
Select item 59176	GRCh38/hg38 2q37.2-37.3(chr2:235268768-242126245)x3	ACKR3, AGAP1 +311 more	Copy number gain	See cases	GPathogenic
Select item 151026	GRCh38/hg38 2q37.3(chr2:236413722-242126251)x1	LOC122889015, LOC122889016 +287 more	Copy number loss	See cases	GPathogenic
Select item 57420	GRCh38/hg38 2q37.3(chr2:236555233-242126245)x1	ACKR3, AGXT +276 more	Copy number loss	See cases	GPathogenic
Select item 1684635	Single allele	LOC122889013, LOC122889014 +274 more	Deletion	Chromosome 2q37 deletion syndrome	GPathogenic
Select item 150710	GRCh38/hg38 2q37.3(chr2:236775762-242126251)x1	AGXT, ANKMY1 +274 more	Copy number loss	See cases	GPathogenic
Select item 57432	GRCh38/hg38 2q37.3(chr2:237643996-242126245)x1	COPS9, CROCC2 +250 more	Copy number loss	See cases	GPathogenic
Select item 151032	GRCh38/hg38 2q37.3(chr2:237902870-242126251)x1	AGXT, ANKMY1 +235 more	Copy number loss	See cases	GPathogenic
Select item 149058	GRCh38/hg38 2q37.3(chr2:238833519-242126245)x1	AGXT, ANKMY1 +185 more	Copy number loss	See cases	GPathogenic
Select item 147508	GRCh38/hg38 2q37.3(chr2:240067206-242126245)x1	AGXT, ANKMY1 +145 more	Copy number loss	See cases	GPathogenic
Select item 149568	GRCh38/hg38 2q37.3(chr2:240187901-242126245)x1	AGXT, ANKMY1 +140 more	Copy number loss	See cases	GLikely pathogenic
Select item 151964	GRCh38/hg38 2q37.3(chr2:240228628-242126245)x1	AGXT, ANKMY1 +140 more	Copy number loss	See cases	GUncertain significance
Select item 152539	GRCh38/hg38 2q37.3(chr2:240671231-242092126)x1	LOC132088835, LOC132088836 +96 more	Copy number loss	See cases	GLikely pathogenic
Select item 144757	GRCh38/hg38 2q37.3(chr2:241481406-242126245)x1	ATG4B, BOK +44 more	Copy number loss	See cases	GUncertain significance
Select item 144361	GRCh38/hg38 2q37.3(chr2:241522479-242126245)x3	ATG4B, BOK +39 more	Copy number gain	See cases	GUncertain significance
Select item 153126	GRCh38/hg38 2q37.3(chr2:241565848-242110155)x1	ATG4B, BOK +32 more	Copy number loss	See cases	GUncertain significance
Select item 147220	GRCh38/hg38 2q37.3(chr2:241910444-242110184)x1	LINC01237, LINC01238 +6 more	Copy number loss	See cases	GBenign
Select item 144460	GRCh38/hg38 2q37.3(chr2:241914437-242126245)x1	LINC01237, LINC01238 +6 more	Copy number loss	See cases	GBenign
Select item 154414	GRCh38/hg38 2q37.3(chr2:241914448-242126251)x1	LINC01237, LINC01238 +6 more	Copy number loss	See cases	GBenign
Select item 150732	GRCh38/hg38 2q37.3(chr2:241914448-242126243)x1	LINC01237, LINC01238 +6 more	Copy number loss	See cases	GBenign
Select item 156829	Single allele	LINC03100, LOC122889016 +6 more	Deletion	Gestational diabetes mellitus uncontrolled +1 more	Gnot provided
Select item 221694	GRCh38/hg38 2q37.3(chr2:241975583-242092368)x0	LINC01237, LOC285097 +6 more	Copy number loss	Premature ovarian failure	GBenign
Select item 156831	NR_110592.1(LINC01238):n.972-495_131503del	LINC01880, LOC132205954 +6 more	Deletion	Large for gestational age +2 more	Gnot provided
Select item 156834	NR_110592.1(LOC102723927):n.2507_131503del	LINC01237, LINC01880 +5 more	Deletion	Gestational diabetes mellitus uncontrolled	Gnot provided
Select item 156835	Single allele	LINC03100, LOC122889016 +5 more	Deletion	Normal pregnancy	Gnot provided
Select item 160979	GRCh38/hg38 2q37.3(chr2:241988449-242126245)x1	LINC01237, LINC01880 +4 more	Copy number loss	See cases	GBenign
Select item 32448	GRCh38/hg38 2q37.3(chr2:241988449-242126245)x1	LINC01237, LINC01880 +4 more	Copy number loss	See cases	GBenign
Select item 145508	GRCh38/hg38 2q37.3(chr2:242011430-242126251)x1	LINC01237, LINC01880 +3 more	Copy number loss	See cases	GBenign/Likely benign

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Items: 34