Related gene-specific medical variations for Gene (Select 56884) - ClinVar - NCBI

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Links from Gene

Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2399824	NM_020116.5(FSTL5):c.130G>A (p.Glu44Lys)	FSTL5, LOC101928052 (E43K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1809215	GRCh37/hg19 4q32.2(chr4:162443332-163119356)x3	FSTL5	Copy number gain	not provided	GUncertain significance
Select item 1808848	GRCh37/hg19 4q32.2(chr4:162134811-162505383)x1	FSTL5	Copy number loss	not provided	GUncertain significance
Select item 980705	GRCh37/hg19 4q32.1-32.2(chr4:161257840-162828600)x3	FSTL5	Copy number gain	not provided	GUncertain significance
Select item 814619	GRCh37/hg19 4q32.2(chr4:162967232-163493491)x3	FSTL5	Copy number gain	not provided	GLikely benign
Select item 689167	GRCh37/hg19 4q32.1-32.2(chr4:160370966-162561746)x3	FSTL5	Copy number gain	not provided	GUncertain significance
Select item 688685	GRCh37/hg19 4q32.2(chr4:162570888-162611000)x1	FSTL5	Copy number loss	not provided	GUncertain significance
Select item 687450	GRCh37/hg19 4q32.2(chr4:162006823-163053043)x1	FSTL5	Copy number loss	not provided	GUncertain significance
Select item 686161	GRCh37/hg19 4q32.2(chr4:162605160-162876877)x1	FSTL5	Copy number loss	not provided	GUncertain significance
Select item 685536	GRCh37/hg19 4q32.2(chr4:162515367-162987364)x1	FSTL5	Copy number loss	not provided	GUncertain significance
Select item 685259	GRCh37/hg19 4q32.2(chr4:162671220-163119235)x1	FSTL5	Copy number loss	not provided	GUncertain significance
Select item 562992	GRCh37/hg19 4q32.2(chr4:162698219-163047747)x1	FSTL5	Copy number loss	not provided	GUncertain significance
Select item 562991	GRCh37/hg19 4q32.2(chr4:162519814-163118339)x1	FSTL5	Copy number loss	not provided	GUncertain significance
Select item 562990	GRCh37/hg19 4q32.2(chr4:161937082-162744835)x1	FSTL5	Copy number loss	not provided	GLikely benign
Select item 524193	t(4;13)(q31;q12)dn	FSTL5	Translocation	not specified	GUncertain significance
Select item 443055	GRCh37/hg19 4q32.2(chr4:162682118-163073720)x1	FSTL5	Copy number loss	See cases	GUncertain significance
Select item 442140	GRCh37/hg19 4q32.2(chr4:162894136-163127979)x1	FSTL5	Copy number loss	See cases	GLikely benign
Select item 155186	GRCh38/hg38 4q32.2(chr4:161650057-161905408)x1	FSTL5	Copy number loss	See cases	GUncertain significance