ClinVar for Gene (Select 653423) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3242300	GRCh37/hg19 8p23.1(chr8:7153587-12245784)x3	BLK, C8orf74 +48 more	Copy number gain	not provided	GPathogenic
Select item 3148928	GRCh37/hg19 8p23.3-22(chr8:158049-16225393)x3	AGPAT5, ANGPT2 +77 more	Copy number gain	See cases	GPathogenic
Select item 3063027	GRCh37/hg19 8p23.3-11.21(chr8:158048-41600696)x3	ADAM18, ADAM2 +234 more	Copy number gain	not specified	GPathogenic
Select item 3063013	GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3	AARD, ABRA +665 more	Copy number gain	not specified	GPathogenic
Select item 2685283	GRCh37/hg19 8p23.3-23.1(chr8:158049-8192683)x1	DEFB104A, DEFB104B +39 more	Copy number loss	not provided	GPathogenic
Select item 2685282	GRCh37/hg19 8p23.3-23.1(chr8:158049-11898696)x1	DEFB105A, DEFB107B +64 more	Copy number loss	not provided	GPathogenic
Select item 2685281	GRCh37/hg19 8p23.3-23.1(chr8:158049-10007143)x1	DEFB1, DEFB107A +46 more	Copy number loss	not provided	GPathogenic
Select item 2685280	GRCh37/hg19 8p23.3-23.1(chr8:158049-8093066)x1	CLN8, CSMD1 +39 more	Copy number loss	not provided	GPathogenic
Select item 2684517	GRCh37/hg19 8p23.2-11.21(chr8:2201405-41723095)x3	SMIM18, SORBS3 +225 more	Copy number gain	not provided	GPathogenic
Select item 2658365	NM_001395484.1(SPAG11A):c.217G>A (p.Asp73Asn)	SPAG11A (D73N +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2580328	GRCh37/hg19 8p23.3-23.1(chr8:10501-11142629)x1	AGPAT5, ANGPT2 +55 more	Copy number loss	See cases	GPathogenic
Select item 2580324	GRCh37/hg19 8p23.1(chr8:7080281-12045269)x3	BLK, C8orf74 +47 more	Copy number gain	8p23.1 duplication syndrome	GPathogenic
Select item 2579290	GRCh38/hg38 8p23.3-21.2(chr8:449893-23854904)x1	LOC126860300, LOC126860301 +720 more	Copy number loss	Neurodevelopmental disorder	GPathogenic
Select item 2390934	NM_001395484.1(SPAG11A):c.209A>G (p.Tyr70Cys)	SPAG11A (Y70C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390932	NM_001395484.1(SPAG11A):c.202C>T (p.Pro68Ser)	SPAG11A (P68S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349486	NM_001395484.1(SPAG11A):c.236G>A (p.Arg79Lys)	SPAG11A (R79K)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 2345605	NM_001395484.1(SPAG11A):c.163C>T (p.Arg55Cys)	SPAG11A (R55C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321551	NM_001395484.1(SPAG11A):c.136C>A (p.Gln46Lys)	SPAG11A (Q46K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292392	NM_001395484.1(SPAG11A):c.169G>T (p.Ala57Ser)	SPAG11A (A57S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1808721	GRCh37/hg19 8p23.3-23.1(chr8:158049-10965627)x1	AGPAT5, ANGPT2 +53 more	Copy number loss	not provided	GPathogenic
Select item 1808083	GRCh37/hg19 8p23.1(chr8:6284373-9047178)x3	AGPAT5, ANGPT2 +33 more	Copy number gain	not provided	GUncertain significance
Select item 1807751	GRCh37/hg19 8p23.3-22(chr8:158049-18936715)x1	AGPAT5, ANGPT2 +93 more	Copy number loss	not provided	GPathogenic
Select item 1711134	Single allele	CDCA2, CLDN23 +250 more	Complex	See cases	GPathogenic
Select item 1708195	GRCh37/hg19 8p23.3-23.1(chr8:158048-11281408)x1	AGPAT5, ANGPT2 +56 more	Copy number loss	See cases	GPathogenic
Select item 1707427	GRCh37/hg19 8p23.3-12(chr8:158048-30187456)x1	ADAM28, ADAM7 +180 more	Copy number loss	See cases	GPathogenic
Select item 1703666	GRCh37/hg19 8p23.3-23.1(chr8:158048-10348413)	AGPAT5, ANGPT2 +46 more	Copy number gain	Neurodevelopmental delay	GPathogenic
Select item 1703665	Single allele	ADAMDEC1, ADGRA2 +251 more	Complex	8p inverted duplication/deletion syndrome	GPathogenic
Select item 1703544	GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)	AARD, ABRA +665 more	Copy number gain	Polydactyly	GPathogenic
Select item 1339975	GRCh37/hg19 8p23.3-23.1(chr8:158048-11936107)x3	AGPAT5, ANGPT2 +64 more	Copy number gain	not provided	GPathogenic
Select item 997076	GRCh37/hg19 8p23.3-11.1(chr8:176814-43396776)	SPAG11A, STMN4 +252 more	Copy number gain	Abnormal fetal cardiovascular morphology	GPathogenic
Select item 974794	GRCh37/hg19 8p23.3-23.1(chr8:176814-11472913)x1	DEFB106B, XKR5 +57 more	Copy number loss	Intellectual disability +1 more	GPathogenic
Select item 815084	GRCh37/hg19 8p23.1(chr8:6999219-8641125)x3	CLDN23, DEFB103A +19 more	Copy number gain	not provided	GUncertain significance
Select item 815083	GRCh37/hg19 8p23.1(chr8:6999219-11895232)x3	DEFB105B, DEFB106A +43 more	Copy number gain	not provided	GPathogenic
Select item 815066	GRCh37/hg19 8p23.3-23.1(chr8:158048-9025197)x1	AGPAT5, ANGPT2 +43 more	Copy number loss	not provided	GPathogenic
Select item 815065	GRCh37/hg19 8p23.3-23.1(chr8:158048-8102819)x3	AGPAT5, ANGPT2 +39 more	Copy number gain	not provided	GPathogenic
Select item 687787	GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3	BAALC, CNOT7 +665 more	Copy number gain	not provided	GPathogenic
Select item 687060	GRCh37/hg19 8p23.3-22(chr8:158048-14214722)x1	USP17L4, USP17L7 +75 more	Copy number loss	not provided	GPathogenic
Select item 684955	GRCh37/hg19 8p23.3-23.1(chr8:158048-9393052)x1	AGPAT5, ANGPT2 +43 more	Copy number loss	not provided	GPathogenic
Select item 625669	GRCh37/hg19 8p23.3-23.1(chr8:194617-7787444)	AGPAT5, ANGPT2 +37 more	Copy number loss	Tetralogy of Fallot	GPathogenic
Select item 625668	GRCh37/hg19 8p23.3-22(chr8:194617-13947374)	DEFB130A, DEFB134 +75 more	Copy number gain	not provided	GPathogenic
Select item 624505	GRCh37/hg19 8p23.3-23.1(chr8:176814-7753583)x1	AGPAT5, ANGPT2 +36 more	Copy number loss	not provided	GLikely pathogenic
Select item 563553	GRCh37/hg19 8p23.3-21.2(chr8:1825200-24533193)x3	ADAM28, ADAM7 +136 more	Copy number gain	not provided	GPathogenic
Select item 563551	GRCh37/hg19 8p23.3-22(chr8:158048-15423270)x3	LONRF1, NEIL2 +76 more	Copy number gain	not provided	GPathogenic
Select item 563550	GRCh37/hg19 8p23.3-22(chr8:158048-13974319)x3	DEFB105A, USP17L1 +75 more	Copy number gain	not provided	GPathogenic
Select item 563548	GRCh37/hg19 8p23.3-22(chr8:168483-13147575)x1,2	MTMR9, MYOM2 +73 more	Copy number gain	not provided	GPathogenic
Select item 563547	GRCh37/hg19 8p23.3-23.1(chr8:158048-10939681)x1	AGPAT5, ANGPT2 +53 more	Copy number loss	not provided	GPathogenic
Select item 563545	GRCh37/hg19 8p23.3-23.1(chr8:158048-9750676)x3	AGPAT5, ANGPT2 +44 more	Copy number gain	not provided	GPathogenic
Select item 563541	GRCh37/hg19 8p23.1(chr8:6999219-11898980)x3	DEFB105B, DEFB106A +43 more	Copy number gain	not provided	GPathogenic
Select item 563525	GRCh37/hg19 8p23.1(chr8:6999219-8881836)x3	CLDN23, DEFB103A +21 more	Copy number gain	not provided	GLikely pathogenic
Select item 443921	GRCh37/hg19 8p23.3-23.1(chr8:158048-9749574)x1	AGPAT5, ANGPT2 +44 more	Copy number loss	See cases	GPathogenic
Select item 442870	GRCh37/hg19 8p23.3-22(chr8:158048-13309069)x1	AGPAT5, ANGPT2 +73 more	Copy number loss	See cases	GLikely pathogenic
Select item 442201	GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771)x3	AARD, ABRA +665 more	Copy number gain	See cases	GPathogenic
Select item 442200	GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771)	FGF20, FGFR1 +665 more	Copy number gain	See cases	GPathogenic
Select item 394884	GRCh37/hg19 8p23.3-q24.3(chr8:158991-146280828)x3	SCRT1, SCX +665 more	Copy number gain	See cases	GPathogenic
Select item 394656	GRCh37/hg19 8p23.3-22(chr8:158991-17536147)x4	AGPAT5, ANGPT2 +86 more	Copy number gain	See cases	GPathogenic
Select item 253407	GRCh37/hg19 8p23.3-22(chr8:158991-13304906)x3	DEFB135, DEFB136 +73 more	Copy number gain	See cases	GPathogenic
Select item 252967	GRCh37/hg19 8p23.3-23.1(chr8:164984-11860845)x3	AGPAT5, ANGPT2 +64 more	Copy number gain	See cases	GPathogenic
Select item 161070	GRCh38/hg38 8p23.1(chr8:7514108-8222398)x3	DEFB103A, DEFB104A +28 more	Copy number gain	See cases	GBenign
Select item 161038	GRCh38/hg38 8p23.3-23.1(chr8:241530-7895064)x1	AGPAT5, ANGPT2 +166 more	Copy number loss	See cases	GPathogenic
Select item 161037	GRCh38/hg38 8p23.2-21.1(chr8:2475295-27504279)x1	ADAM28, ADAM7 +773 more	Copy number loss	See cases	GPathogenic
Select item 161036	GRCh38/hg38 8p23.3-23.1(chr8:241530-7895064)x3	AGPAT5, ANGPT2 +166 more	Copy number gain	See cases	GPathogenic
Select item 161012	GRCh38/hg38 8p23.1(chr8:7411297-8222398)x1	DEFB103A, DEFB103B +35 more	Copy number loss	See cases	GBenign
Select item 161011	GRCh38/hg38 8p23.1(chr8:7411297-8222398)x3	DEFB103A, DEFB103B +35 more	Copy number gain	See cases	GBenign
Select item 161010	GRCh38/hg38 8p23.1(chr8:7411297-7895064)x1	DEFB103A, DEFB103B +26 more	Copy number loss	See cases	GBenign
Select item 160912	GRCh38/hg38 8p23.1(chr8:7411297-7895064)x3	DEFB103A, DEFB103B +26 more	Copy number gain	See cases	GBenign
Select item 155181	GRCh38/hg38 8p23.3-23.1(chr8:226452-12698554)x3	LOC129999827, LOC129999828 +393 more	Copy number gain	See cases	GPathogenic
Select item 154906	GRCh38/hg38 8p23.1(chr8:7300731-7948701)x1	DEFB103A, DEFB103B +34 more	Copy number loss	See cases	GBenign
Select item 154894	GRCh38/hg38 8p23.1(chr8:6786638-8364508)x3	DEFA1, DEFA1B +73 more	Copy number gain	See cases	GBenign
Select item 154791	GRCh38/hg38 8p23.3-q24.3(chr8:226452-145068712)x3	AARD, ABRA +3663 more	Copy number gain	See cases	GPathogenic
Select item 154780	GRCh38/hg38 8p23.1(chr8:7256137-7981415)x1	DEFB103A, DEFB103B +43 more	Copy number loss	See cases	GBenign
Select item 154529	GRCh38/hg38 8p23.3-23.1(chr8:241530-10458484)x1	AGPAT5, ANGPT2 +256 more	Copy number loss	See cases	GPathogenic
Select item 154431	GRCh38/hg38 8p23.1(chr8:7311988-8273109)x3	FAM90A17, FAM90A18 +48 more	Copy number gain	See cases	GBenign
Select item 154427	GRCh38/hg38 8p23.1(chr8:7381949-7948705)x1	DEFB103A, DEFB103B +28 more	Copy number loss	See cases	GBenign
Select item 154417	GRCh38/hg38 8p23.1(chr8:7512656-7895074)x1	DEFB103A, DEFB104A +19 more	Copy number loss	See cases	GBenign
Select item 154415	GRCh38/hg38 8p23.1(chr8:7411303-7948705)x3	DEFB103A, DEFB103B +27 more	Copy number gain	See cases	GBenign
Select item 154409	GRCh38/hg38 8p23.1(chr8:7195674-7948705)x1	DEFB103A, DEFB103B +41 more	Copy number loss	See cases	GBenign
Select item 154404	GRCh38/hg38 8p23.1(chr8:7311988-7948705)x1	DEFB103A, DEFB103B +34 more	Copy number loss	See cases	GBenign
Select item 154403	GRCh38/hg38 8p23.1(chr8:7311988-7948705)x3	DEFB103A, DEFB103B +34 more	Copy number gain	See cases	GBenign
Select item 154367	GRCh38/hg38 8p23.1(chr8:7381949-7895074)x1	DEFB103A, DEFB103B +27 more	Copy number loss	See cases	GBenign
Select item 154364	GRCh38/hg38 8p23.1(chr8:7311988-7895074)x3	DEFB103A, DEFB103B +33 more	Copy number gain	See cases	GBenign
Select item 154363	GRCh38/hg38 8p23.1(chr8:7311988-8222390)x1	DEFB103A, DEFB103B +42 more	Copy number loss	See cases	GBenign
Select item 154362	GRCh38/hg38 8p23.1(chr8:7311988-8222390)x3	DEFB103A, DEFB103B +42 more	Copy number gain	See cases	GBenign
Select item 154354	GRCh38/hg38 8p23.1(chr8:7195674-7895074)x1	DEFB103A, DEFB103B +40 more	Copy number loss	See cases	GBenign
Select item 154342	GRCh38/hg38 8p23.1(chr8:7256134-8188790)x1	DEFB103A, DEFB103B +48 more	Copy number loss	See cases	GBenign
Select item 154336	GRCh38/hg38 8p23.1(chr8:7311988-7895074)x1	DEFB103A, DEFB103B +33 more	Copy number loss	See cases	GBenign
Select item 154334	GRCh38/hg38 8p23.1(chr8:7195674-8222390)x1	DEFB103A, DEFB103B +49 more	Copy number loss	See cases	GBenign
Select item 154327	GRCh38/hg38 8p23.1(chr8:7381949-8222390)x1	DEFB103A, DEFB103B +36 more	Copy number loss	See cases	GBenign
Select item 154326	GRCh38/hg38 8p23.1(chr8:7381949-8222390)x3	DEFB103A, DEFB103B +36 more	Copy number gain	See cases	GBenign
Select item 153413	GRCh38/hg38 8p23.3-q24.3(chr8:208048-145070385)x3	LOC126860438, LOC126860439 +3663 more	Copy number gain	See cases	GPathogenic
Select item 153029	GRCh38/hg38 8p23.1(chr8:7311968-8222398)x3	DEFB103A, DEFB103B +42 more	Copy number gain	See cases	GBenign
Select item 153028	GRCh38/hg38 8p23.1(chr8:7381969-7948707)x1	DEFB103A, DEFB103B +28 more	Copy number loss	See cases	GBenign
Select item 152994	GRCh38/hg38 8p23.1(chr8:7381969-8222339)x1	DEFB103A, DEFB103B +36 more	Copy number loss	See cases	GBenign
Select item 152969	GRCh38/hg38 8p23.1(chr8:7514108-7948707)x3	DEFB103A, DEFB104A +20 more	Copy number gain	See cases	GBenign
Select item 152917	GRCh38/hg38 8p23.3-22(chr8:226452-16280146)x3	LOC101929290, LOC102723313 +448 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 151133	GRCh38/hg38 8p23.1-11.22(chr8:7141697-38695546)x3	DPYSL2, DUSP26 +1020 more	Copy number gain	See cases	GPathogenic
Select item 151040	GRCh38/hg38 8p23.1(chr8:7546074-8222390)x3	DEFB103A, DEFB104A +27 more	Copy number gain	See cases	GBenign
Select item 150887	GRCh38/hg38 8p23.1(chr8:7205665-7948701)x3	DEFB103A, DEFB103B +41 more	Copy number gain	See cases	GBenign
Select item 150441	GRCh38/hg38 8p23.1(chr8:7142958-7895074)x3	DEFB103A, DEFB103B +40 more	Copy number gain	See cases	GBenign
Select item 150403	GRCh38/hg38 8p23.1(chr8:7300731-7981415)x3	DEFB103A, DEFB103B +37 more	Copy number gain	See cases	GBenign

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