GDF10[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 152998	GRCh38/hg38 10p15.1-q11.22(chr10:4604734-48074662)x3	AGAP4, AGAP9 +1221 more	Copy number gain	See cases	GBenign
Select item 154900	GRCh38/hg38 10q11.21-21.3(chr10:42112187-67400675)x3	A1CF, ADO +561 more	Copy number gain	See cases	GPathogenic
Select item 145479	GRCh38/hg38 10q11.21-11.23(chr10:42395201-50877059)x3	LOC130003758, LOC130003759 +309 more	Copy number gain	See cases	GPathogenic
Select item 145481	GRCh38/hg38 10q11.21-22.2(chr10:42685306-73715908)x3	A1CF, ADAMTS14 +902 more	Copy number gain	See cases	GPathogenic
Select item 144977	GRCh38/hg38 10q11.21-21.1(chr10:42884294-52265317)x3	FAM170B, FAM170B-AS1 +306 more	Copy number gain	See cases	GPathogenic
Select item 2498203	NC_000010.11:g.45704708_(49974954_50015268)del	AGAP4, AGAP6 +122 more	Deletion	10q11.22q11.23 deletion syndrome	GLikely pathogenic
Select item 154709	GRCh38/hg38 10q11.22-11.23(chr10:45710242-49929364)x1	AGAP10, AGAP4 +118 more	Copy number loss	See cases	GPathogenic
Select item 58543	GRCh38/hg38 10q11.22-11.23(chr10:45710242-50151325)x1	AGAP10, AGAP4 +125 more	Copy number loss	See cases	GPathogenic
Select item 146781	GRCh38/hg38 10q11.22-11.23(chr10:45710248-50021141)x1	RBP3, SLC18A3 +123 more	Copy number loss	See cases	GPathogenic
Select item 151967	GRCh38/hg38 10q11.22-11.23(chr10:45788078-50066466)x1	AGAP10, AGAP4 +122 more	Copy number loss	See cases	GUncertain significance
Select item 3235900	GRCh38/hg38 10q11.22-11.23(chr10:45795500-50134000)	AGAP4, AGAP6 +122 more	Copy number loss	Pulmonary arterial hypertension	GLikely pathogenic
Select item 148682	GRCh38/hg38 10q11.22-11.23(chr10:45810008-50066466)x1	AGAP10, AGAP4 +121 more	Copy number loss	See cases	GLikely pathogenic
Select item 154220	GRCh38/hg38 10q11.22-11.23(chr10:45931517-50035809)x3	AGAP10, AGAP6 +119 more	Copy number gain	See cases	GUncertain significance
Select item 150121	GRCh38/hg38 10q11.22-11.23(chr10:45931517-49929364)x1	AGAP10, AGAP9 +114 more	Copy number loss	See cases	GLikely pathogenic
Select item 149971	GRCh38/hg38 10q11.22-11.23(chr10:45931517-49929364)x1	AGAP9, ANTXRL +113 more	Copy number loss	See cases	GLikely pathogenic
Select item 144985	GRCh38/hg38 10q11.22-11.23(chr10:45931517-49929364)x1	AGAP10, AGAP9 +114 more	Copy number loss	See cases	GPathogenic
Select item 58551	GRCh38/hg38 10q11.22-11.23(chr10:45931517-50655311)x1	AGAP6, AGAP9 +147 more	Copy number loss	See cases	GPathogenic
Select item 150503	GRCh38/hg38 10q11.22-11.23(chr10:45999930-49937908)x1	AGAP9, ANTXRL +112 more	Copy number loss	See cases	GLikely pathogenic
Select item 58548	GRCh38/hg38 10q11.22-11.23(chr10:45999930-49937908)x1	AGAP9, ANTXRL +112 more	Copy number loss	See cases	GUncertain significance
Select item 57411	GRCh38/hg38 10q11.22-11.23(chr10:45999930-49937908)x3	AGAP9, ANTXRL +112 more	Copy number gain	See cases	GPathogenic
Select item 150650	GRCh38/hg38 10q11.22(chr10:46146977-47987500)x3	AGAP10, AGAP9 +35 more	Copy number gain	See cases	GBenign
Select item 146825	GRCh38/hg38 10q11.22(chr10:46146977-47987500)x3	AGAP9, ANTXRL +34 more	Copy number gain	See cases	GBenign
Select item 545135	Single allele	LOC130003791, LOC130003792 +109 more	Duplication	Schizophrenia	GLikely pathogenic
Select item 161043	GRCh38/hg38 10q11.22(chr10:46157935-47923579)x1	AGAP10, AGAP9 +34 more	Copy number loss	See cases	GBenign
Select item 161022	GRCh38/hg38 10q11.22(chr10:46157935-47923579)x3	AGAP10, AGAP9 +34 more	Copy number gain	See cases	GBenign
Select item 160988	GRCh38/hg38 10q11.22(chr10:46157935-47923579)x3	AGAP10, AGAP9 +34 more	Copy number gain	See cases	GBenign
Select item 154864	GRCh38/hg38 10q11.22(chr10:46157935-47923579)x3	AGAP10, AGAP9 +34 more	Copy number gain	See cases	GBenign
Select item 154844	GRCh38/hg38 10q11.22(chr10:46157935-47923579)x1	AGAP10, AGAP9 +34 more	Copy number loss	See cases	GBenign
Select item 150698	GRCh38/hg38 10q11.22(chr10:46157935-47923579)x3	AGAP9, ANTXRL +33 more	Copy number gain	See cases	GBenign
Select item 150663	GRCh38/hg38 10q11.22(chr10:46157935-47923579)x3	AGAP10, AGAP9 +34 more	Copy number gain	See cases	GBenign
Select item 150472	GRCh38/hg38 10q11.22(chr10:46157935-47923579)x3	AGAP10, AGAP9 +34 more	Copy number gain	See cases	GBenign
Select item 150205	GRCh38/hg38 10q11.22(chr10:46157935-47923579)x3	AGAP10, AGAP9 +34 more	Copy number gain	See cases	GBenign
Select item 149982	GRCh38/hg38 10q11.22(chr10:46157935-47923579)x3	AGAP10, AGAP9 +34 more	Copy number gain	See cases	GBenign
Select item 149897	GRCh38/hg38 10q11.22(chr10:46157935-47923579)x3	AGAP10, AGAP9 +34 more	Copy number gain	See cases	GBenign
Select item 148133	GRCh38/hg38 10q11.22(chr10:46157935-47923579)x3	AGAP10, AGAP9 +34 more	Copy number gain	See cases	GBenign
Select item 148103	GRCh38/hg38 10q11.22(chr10:46157935-48054380)x3	AGAP10, AGAP9 +36 more	Copy number gain	See cases	GBenign
Select item 147214	GRCh38/hg38 10q11.22(chr10:46157935-47923579)x3	AGAP10, AGAP9 +34 more	Copy number gain	See cases	GBenign
Select item 146806	GRCh38/hg38 10q11.22(chr10:46157935-47923579)x1	AGAP10, AGAP9 +34 more	Copy number loss	See cases	GBenign
Select item 146805	GRCh38/hg38 10q11.22(chr10:46157935-47923579)x3	AGAP10, AGAP9 +34 more	Copy number gain	See cases	GBenign
Select item 146700	GRCh38/hg38 10q11.22(chr10:46157935-47923579)x3	AGAP10, AGAP9 +34 more	Copy number gain	See cases	GBenign
Select item 145488	GRCh38/hg38 10q11.22(chr10:46157935-47923579)x3	AGAP10, AGAP9 +34 more	Copy number gain	See cases	GBenign
Select item 145457	GRCh38/hg38 10q11.22(chr10:46157935-47923579)x3	AGAP10, AGAP9 +34 more	Copy number gain	See cases	GBenign
Select item 144354	GRCh38/hg38 10q11.22(chr10:46157935-47923579)x3	AGAP10, AGAP9 +34 more	Copy number gain	See cases	GBenign
Select item 144187	GRCh38/hg38 10q11.22(chr10:46157935-47923579)x3	AGAP9, ANTXRL +33 more	Copy number gain	See cases	GBenign
Select item 33676	GRCh38/hg38 10q11.22(chr10:46157935-47923579)x3	AGAP10, AGAP9 +34 more	Copy number gain	See cases	GBenign
Select item 32820	GRCh38/hg38 10q11.22(chr10:46157935-47923579)x3	AGAP10, AGAP9 +34 more	Copy number gain	See cases	GBenign
Select item 32321	GRCh38/hg38 10q11.22(chr10:46157935-47923579)x3	AGAP10, AGAP9 +34 more	Copy number gain	See cases	GBenign
Select item 32317	GRCh38/hg38 10q11.22(chr10:46157935-47923579)x3	AGAP10, AGAP9 +34 more	Copy number gain	See cases	GBenign
Select item 31951	GRCh38/hg38 10q11.22(chr10:46157935-47923579)x1	GDF2, GPRIN2 +34 more	Copy number loss	See cases	GBenign
Select item 154978	GRCh38/hg38 10q11.22(chr10:46375049-47987500)x3	AGAP10, AGAP9 +30 more	Copy number gain	See cases	GBenign
Select item 154430	GRCh38/hg38 10q11.22(chr10:46375049-47987500)x3	AGAP9, ANXA8 +29 more	Copy number gain	See cases	GBenign
Select item 153030	GRCh38/hg38 10q11.22(chr10:46375049-47987500)x3	AGAP10, AGAP9 +30 more	Copy number gain	See cases	GBenign
Select item 32955	GRCh38/hg38 10q11.22(chr10:46375049-47987500)x1	AGAP9, ANXA8 +29 more	Copy number loss	See cases	GBenign
Select item 148137	GRCh38/hg38 10q11.22(chr10:46489780-47923579)x1	AGAP10, AGAP9 +26 more	Copy number loss	See cases	GBenign
Select item 145472	GRCh38/hg38 10q11.22(chr10:46489780-47923579)x3	AGAP10, AGAP9 +26 more	Copy number gain	See cases	GBenign/Likely benign
Select item 145409	GRCh38/hg38 10q11.22(chr10:46489780-47923579)x3	SYT15B, ZNF488 +26 more	Copy number gain	See cases	GBenign
Select item 154420	GRCh38/hg38 10q11.22(chr10:46490281-47923579)x1	AGAP10, AGAP9 +26 more	Copy number loss	See cases	GBenign
Select item 154419	GRCh38/hg38 10q11.22(chr10:46490281-47923579)x3	AGAP10, AGAP9 +26 more	Copy number gain	See cases	GBenign
Select item 148134	GRCh38/hg38 10q11.22(chr10:46490281-47923579)x3	AGAP10, AGAP9 +26 more	Copy number gain	See cases	GBenign
Select item 145473	GRCh38/hg38 10q11.22(chr10:46490281-47923579)x1	AGAP10, AGAP9 +26 more	Copy number loss	See cases	GBenign
Select item 144481	GRCh38/hg38 10q11.22(chr10:46490281-48074662)x1	AGAP10, AGAP9 +28 more	Copy number loss	See cases	GLikely benign
Select item 2545455	NM_004962.5(GDF10):c.40C>A (p.Pro14Thr)	GDF10 (P14T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099227	NM_004962.5(GDF10):c.62T>C (p.Leu21Pro)	GDF10 (L21P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2267020	NM_004962.5(GDF10):c.193G>A (p.Ala65Thr)	GDF10 (A65T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241320	NM_004962.5(GDF10):c.221T>C (p.Met74Thr)	GDF10 (M74T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272008	NM_004962.5(GDF10):c.235A>G (p.Met79Val)	GDF10 (M79V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099222	NM_004962.5(GDF10):c.283G>A (p.Gly95Arg)	GDF10 (G95R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515595	NM_004962.5(GDF10):c.314G>C (p.Arg105Thr)	GDF10 (R105T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099223	NM_004962.5(GDF10):c.338C>T (p.Ala113Val)	GDF10 (A113V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099224	NM_004962.5(GDF10):c.340G>A (p.Val114Met)	GDF10 (V114M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099225	NM_004962.5(GDF10):c.374C>T (p.Ser125Leu)	GDF10 (S125L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099226	NM_004962.5(GDF10):c.491T>C (p.Leu164Pro)	GDF10 (L164P)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2236658	NM_004962.5(GDF10):c.627C>G (p.Ile209Met)	GDF10 (I209M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099228	NM_004962.5(GDF10):c.667G>A (p.Ala223Thr)	GDF10 (A223T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321872	NM_004962.5(GDF10):c.668C>T (p.Ala223Val)	GDF10 (A223V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461323	NM_004962.5(GDF10):c.694C>G (p.Pro232Ala)	GDF10 (P232A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235018	NM_004962.5(GDF10):c.775G>A (p.Val259Met)	GDF10 (V259M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367322	NM_004962.5(GDF10):c.862G>A (p.Val288Met)	GDF10 (V288M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2479303	NM_004962.5(GDF10):c.890C>G (p.Pro297Arg)	GDF10 (P297R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099229	NM_004962.5(GDF10):c.893T>G (p.Leu298Arg)	GDF10 (L298R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099230	NM_004962.5(GDF10):c.899A>G (p.Asp300Gly)	GDF10 (D300G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548773	NM_004962.5(GDF10):c.910C>G (p.Pro304Ala)	GDF10 (P304A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 768363	NM_004962.5(GDF10):c.912G>A (p.Pro304=)	GDF10	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2458136	NM_004962.5(GDF10):c.955C>T (p.His319Tyr)	GDF10 (H319Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2313112	NM_004962.5(GDF10):c.974C>T (p.Pro325Leu)	GDF10 (P325L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548774	NM_004962.5(GDF10):c.989C>G (p.Ala330Gly)	GDF10 (A330G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546894	NM_004962.5(GDF10):c.1000C>G (p.Arg334Gly)	GDF10 (R334G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 786156	NM_004962.5(GDF10):c.1045A>G (p.Met349Val)	GDF10 (M349V)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3099219	NM_004962.5(GDF10):c.1089G>C (p.Gln363His)	GDF10 (Q363H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 161627	NM_004962.5(GDF10):c.1217C>T (p.Ala406Val)	GDF10 (A406V)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 2463551	NM_004962.5(GDF10):c.1222G>T (p.Ala408Ser)	GDF10 (A408S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2609287	NM_004962.5(GDF10):c.1349C>G (p.Ser450Cys)	GDF10 (S450C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462065	NM_004962.5(GDF10):c.1379G>A (p.Arg460Gln)	GDF10 (R460Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099221	NM_004962.5(GDF10):c.1382A>C (p.Asn461Thr)	GDF10 (N461T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339629	NM_004962.5(GDF10):c.1387G>A (p.Val463Ile)	GDF10 (V463I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3148882	GRCh37/hg19 10q11.22-11.23(chr10:46975077-51089085)x3	AGAP10, AGAP9 +28 more	Copy number gain	See cases	GUncertain significance
Select item 2684603	GRCh37/hg19 10q11.22-11.23(chr10:48349961-51817663)x3	AGAP6, ARHGAP22 +25 more	Copy number gain	not provided	GUncertain significance
Select item 2684602	GRCh37/hg19 10q11.21-24.2(chr10:42709645-100834951)x3	RRP12, RTKN2 +332 more	Copy number gain	not provided	GPathogenic
Select item 2580332	GRCh37/hg19 10q11.22-11.23(chr10:46284269-51870080)x1	AGAP10, AGAP4 +37 more	Copy number loss	See cases	GPathogenic
Select item 2574696	GRCh37/hg19 10p14-q26.3(chr10:11138692-135427143)	MTG1, NPS +679 more	Copy number gain	Distal trisomy 10q	GPathogenic

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