"GeneDx"[submitter] AND "GNRH1"[gene] - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59735	GRCh38/hg38 8p23.3-12(chr8:96310-30614703)x3	ADAM28, ADAM7 +979 more	Copy number gain	See cases	GPathogenic
Select item 152909	GRCh38/hg38 8p23.3-12(chr8:226452-34491890)x3	LOC130000099, LOC130000100 +1040 more	Copy number gain	See cases	GPathogenic
Select item 59766	GRCh38/hg38 8p23.1-11.1(chr8:12750796-43532444)x3	ADAM18, ADAM2 +922 more	Copy number gain	See cases	GPathogenic
Select item 59769	GRCh38/hg38 8p22-q11.21(chr8:14940110-47929925)x3	LOC130000309, LOC130000310 +900 more	Copy number gain	See cases	GPathogenic
Select item 58413	GRCh38/hg38 8p21.2(chr8:23961808-25436108)x3	ADAM28, ADAM7 +26 more	Copy number gain	See cases	GUncertain significance
Select item 60359	GRCh38/hg38 8p21.2-12(chr8:24910364-31210737)x1	ADRA1A, BNIP3L +259 more	Copy number loss	See cases	GPathogenic
Select item 1195648	NC_000008.11:g.25419218C>T	GNRH1	Single nucleotide variant	not provided	GLikely benign
Select item 1204009	NM_001083111.2(GNRH1):c.238-179dup	GNRH1	Duplication (intron variant)	not provided	GLikely benign
Select item 1185918	NM_001083111.2(GNRH1):c.141+281A>G	GNRH1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1214136	NM_001083111.2(GNRH1):c.141+202A>G	GNRH1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1255191	NM_001083111.2(GNRH1):c.141+85A>G	GNRH1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1230178	NM_001083111.2(GNRH1):c.141+40T>G	GNRH1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1229585	NC_000008.11:g.25425076T>C	GNRH1	Single nucleotide variant	not provided	GBenign
Select item 1211454	NC_000008.11:g.25425267dup	GNRH1	Duplication	not provided	GLikely benign
Select item 1262901	NC_000008.11:g.25425333A>G	GNRH1	Single nucleotide variant	not provided	GBenign
Select item 253392	GRCh37/hg19 8p23.1-21.2(chr8:12580132-26774307)x3	ADAM28, ADAM7 +82 more	Copy number gain	See cases	GPathogenic