"GeneDx"[submitter] AND "DNAJC13"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 152454	GRCh38/hg38 3q22.1-23(chr3:129817243-141425155)x1	A4GNT, ACAD11 +282 more	Copy number loss	See cases	GPathogenic
Select item 1286197	NM_015268.4(DNAJC13):c.-13-317dup	DNAJC13	Duplication (intron variant)	not provided	GBenign
Select item 1265743	NM_015268.4(DNAJC13):c.-13-266G>C	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1265563	NM_015268.4(DNAJC13):c.-13-249C>G	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1230766	NM_015268.4(DNAJC13):c.-13-206_-13-194del	DNAJC13	Deletion (intron variant)	not provided	GBenign
Select item 1283119	NM_015268.4(DNAJC13):c.-13-140dup	DNAJC13	Duplication (intron variant)	not provided	GBenign
Select item 1293955	NM_015268.4(DNAJC13):c.-13-49_-13-48insAG	DNAJC13	Insertion (intron variant)	not provided	GBenign
Select item 1245418	NM_015268.4(DNAJC13):c.68+150A>G	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1263992	NM_015268.4(DNAJC13):c.69-264T>A	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1230045	NM_015268.4(DNAJC13):c.69-141A>T	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1249398	NM_015268.4(DNAJC13):c.144+209del	DNAJC13	Deletion (intron variant)	not provided	GBenign
Select item 1251735	NM_015268.4(DNAJC13):c.145-160A>G	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1210107	NM_015268.4(DNAJC13):c.246T>G (p.Thr82=)	DNAJC13	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1293993	NM_015268.4(DNAJC13):c.294+167C>T	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1258123	NM_015268.4(DNAJC13):c.336+111G>A	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1293951	NM_015268.4(DNAJC13):c.336+232C>T	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1283403	NM_015268.4(DNAJC13):c.537+26dup	DNAJC13	Duplication (intron variant)	not provided	GBenign
Select item 1272004	NM_015268.4(DNAJC13):c.537+14T>A	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1286886	NM_015268.4(DNAJC13):c.538-34A>T	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1183713	NM_015268.4(DNAJC13):c.744+47C>T	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 767932	NM_015268.4(DNAJC13):c.932+16del	DNAJC13	Deletion (intron variant)	not provided	GBenign
Select item 1263155	NM_015268.4(DNAJC13):c.932+280G>A	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1252150	NM_015268.4(DNAJC13):c.933-320A>G	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1273243	NM_015268.4(DNAJC13):c.1349+102C>T	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1237746	NM_015268.4(DNAJC13):c.1349+103C>A	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1182502	NM_015268.4(DNAJC13):c.1449+45C>G	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1293950	NM_015268.4(DNAJC13):c.1449+98G>C	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1249456	NM_015268.4(DNAJC13):c.1449+179C>T	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 767933	NM_015268.4(DNAJC13):c.1450-9dup	DNAJC13	Duplication (intron variant)	not provided	GBenign
Select item 1240697	NM_015268.4(DNAJC13):c.1557+34T>C	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1256917	NM_015268.4(DNAJC13):c.1557+194T>C	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1276998	NM_015268.4(DNAJC13):c.1558-243C>T	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1234786	NM_015268.4(DNAJC13):c.1558-207_1558-199del	DNAJC13	Deletion (intron variant)	not provided	GBenign
Select item 1270351	NM_015268.4(DNAJC13):c.1770+127T>G	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1276325	NM_015268.4(DNAJC13):c.1770+285T>C	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1249225	NM_015268.4(DNAJC13):c.1771-96del	DNAJC13	Deletion (intron variant)	not provided	GBenign
Select item 1293944	NM_015268.4(DNAJC13):c.1892+257A>G	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1177734	NM_015268.4(DNAJC13):c.2064+176T>A	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1293960	NM_015268.4(DNAJC13):c.2208+30G>A	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1263399	NM_015268.4(DNAJC13):c.2291+58T>C	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1279810	NM_015268.4(DNAJC13):c.2292-316dup	DNAJC13	Duplication (intron variant)	not provided	GBenign
Select item 1279764	NM_015268.4(DNAJC13):c.2292-277del	DNAJC13	Deletion (intron variant)	not provided	GBenign
Select item 1297822	NM_015268.4(DNAJC13):c.2292-108_2292-106del	DNAJC13	Deletion (intron variant)	not provided	GBenign
Select item 1270837	NM_015268.4(DNAJC13):c.2292-107_2292-106del	DNAJC13	Deletion (intron variant)	not provided	GBenign
Select item 1262022	NM_015268.4(DNAJC13):c.2292-109_2292-106del	DNAJC13	Deletion (intron variant)	not provided	GBenign
Select item 1245473	NM_015268.4(DNAJC13):c.2292-106del	DNAJC13	Deletion (intron variant)	not provided	GBenign
Select item 1229655	NM_015268.4(DNAJC13):c.2292-107C>T	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1297821	NM_015268.4(DNAJC13):c.2292-89_2292-88dup	DNAJC13	Duplication (intron variant)	not provided	GBenign
Select item 1231088	NM_015268.4(DNAJC13):c.2292-106C>T	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1261936	NM_015268.4(DNAJC13):c.2445+72T>A	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1293964	NM_015268.4(DNAJC13):c.2445+153G>T	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1277056	NM_015268.4(DNAJC13):c.2446-272C>T	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1233462	NM_015268.4(DNAJC13):c.2549+25G>A	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1210029	NM_015268.4(DNAJC13):c.2550-9A>T	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1255091	NM_015268.4(DNAJC13):c.2710-272C>G	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1259611	NM_015268.4(DNAJC13):c.2710-76T>G	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1266915	NM_015268.4(DNAJC13):c.2710-14A>G	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1242088	NM_015268.4(DNAJC13):c.2772+23C>T	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1266759	NM_015268.4(DNAJC13):c.2875-351T>G	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1289905	NM_015268.4(DNAJC13):c.2980-206C>T	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1249739	NM_015268.4(DNAJC13):c.3182+28T>A	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1278791	NM_015268.4(DNAJC13):c.3267+79T>C	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1293973	NM_015268.4(DNAJC13):c.3267+167C>T	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1289826	NM_015268.4(DNAJC13):c.3422+72T>C	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1233468	NM_015268.4(DNAJC13):c.3422+258A>G	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1266241	NM_015268.4(DNAJC13):c.3469-86T>A	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1282465	NM_015268.4(DNAJC13):c.3651C>T (p.Ala1217=)	DNAJC13	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1262107	NM_015268.4(DNAJC13):c.3825+288T>C	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1233977	NM_015268.4(DNAJC13):c.3826-320dup	DNAJC13	Duplication (intron variant)	not provided	GBenign
Select item 1293956	NM_015268.4(DNAJC13):c.3826-303A>G	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1279966	NM_015268.4(DNAJC13):c.3942-152del	DNAJC13	Deletion (intron variant)	not provided	GBenign
Select item 1233787	NM_015268.4(DNAJC13):c.4020+186C>T	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1242285	NM_015268.4(DNAJC13):c.4156+264G>A	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1183164	NM_015268.4(DNAJC13):c.4157-267G>A	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1273834	NM_015268.4(DNAJC13):c.4157-174G>A	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1210022	NM_015268.4(DNAJC13):c.4157-13T>G	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1293945	NM_015268.4(DNAJC13):c.4341+42C>T	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1233327	NM_015268.4(DNAJC13):c.4342-135dup	DNAJC13	Duplication (intron variant)	not provided	GBenign
Select item 1209902	NM_015268.4(DNAJC13):c.4387G>T (p.Ala1463Ser)	DNAJC13 (A1463S +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1179668	NM_015268.4(DNAJC13):c.4416+172T>C	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1229280	NM_015268.4(DNAJC13):c.4416+231T>C	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1293962	NM_015268.4(DNAJC13):c.4417-84T>C	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1277871	NM_015268.4(DNAJC13):c.4537-41del	DNAJC13	Deletion (intron variant)	not provided	GBenign
Select item 1221771	NM_015268.4(DNAJC13):c.4885-163T>C	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1210040	NM_015268.4(DNAJC13):c.4885-18G>A	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1209984	NM_015268.4(DNAJC13):c.5018A>G (p.Tyr1673Cys)	DNAJC13 (Y1673C +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1235275	NM_015268.4(DNAJC13):c.5116-203A>G	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1277734	NM_015268.4(DNAJC13):c.5293+22C>T	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1179309	NM_015268.4(DNAJC13):c.5386-139T>A	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1264478	NM_015268.4(DNAJC13):c.5485+158G>A	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1255197	NM_015268.4(DNAJC13):c.5485+198G>C	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1283718	NM_015268.4(DNAJC13):c.5486-280A>G	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1264251	NM_015268.4(DNAJC13):c.5486-244G>T	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1258182	NM_015268.4(DNAJC13):c.5486-222A>C	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1230866	NM_015268.4(DNAJC13):c.5486-219A>G	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1238752	NM_015268.4(DNAJC13):c.5486-189C>T	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1210109	NM_015268.4(DNAJC13):c.5560+4A>T	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1242170	NM_015268.4(DNAJC13):c.5673+134C>G	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1247215	NM_015268.4(DNAJC13):c.5673+330G>A	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1247208	NM_015268.4(DNAJC13):c.5674-162C>T	DNAJC13	Single nucleotide variant (intron variant)	not provided	GBenign

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