CENPV[gene] - ClinVar

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Items: 63

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58693	GRCh38/hg38 17p12-11.2(chr17:10892259-17964282)x3	LOC130060335, LOC130060336 +242 more	Copy number gain	See cases	GPathogenic
Select item 1707454	Single allele	ADORA2B, ARHGAP44 +228 more	Duplication	not specified	GPathogenic
Select item 154979	GRCh38/hg38 17p12-11.2(chr17:15066799-17472457)x1	ADORA2B, CCDC144A +137 more	Copy number loss	See cases	GPathogenic
Select item 148088	GRCh38/hg38 17p12-11.2(chr17:15210400-18280816)x3	LOC284191, LRRC75A +216 more	Copy number gain	See cases	GPathogenic
Select item 58104	GRCh38/hg38 17p12-11.2(chr17:15234685-20620700)x3	ADORA2B, AKAP10 +333 more	Copy number gain	See cases	GPathogenic
Select item 58107	GRCh38/hg38 17p12-11.2(chr17:15259164-20925299)x3	ADORA2B, AKAP10 +337 more	Copy number gain	See cases	GPathogenic
Select item 153990	GRCh38/hg38 17p12-11.2(chr17:15552362-19014200)x3	ADORA2B, ALKBH5 +240 more	Copy number gain	See cases	GPathogenic
Select item 155418	GRCh38/hg38 17p12-11.2(chr17:15729893-20510251)x1	LOC126862516, LOC126862517 +314 more	Copy number loss	See cases	GPathogenic
Select item 56996	GRCh38/hg38 17p12-11.2(chr17:15776915-18771753)x1	LOC130060335, LOC130060336 +217 more	Copy number loss	See cases	GPathogenic
Select item 153341	GRCh38/hg38 17p12-11.2(chr17:15784832-16860143)x3	ADORA2B, CCDC144A +64 more	Copy number gain	See cases	GUncertain significance
Select item 155583	GRCh38/hg38 17p12-11.2(chr17:15850859-20649235)x1	FAM106C, FAM83G +311 more	Copy number loss	See cases	GPathogenic
Select item 155110	GRCh38/hg38 17p12-11.2(chr17:15883037-20658018)x1	ADORA2B, AKAP10 +311 more	Copy number loss	See cases	GPathogenic
Select item 150691	GRCh38/hg38 17p12-11.2(chr17:15883037-20620700)x1	ADORA2B, AKAP10 +311 more	Copy number loss	See cases	GPathogenic
Select item 57018	GRCh38/hg38 17p12-11.2(chr17:15898032-20620700)x1	ADORA2B, AKAP10 +311 more	Copy number loss	See cases	GPathogenic
Select item 60429	GRCh38/hg38 17p12-11.2(chr17:15952071-18362819)x1	ADORA2B, ALKBH5 +199 more	Copy number loss	See cases	GPathogenic
Select item 60433	GRCh38/hg38 17p11.2(chr17:16117885-18362819)x1	ALKBH5, ATPAF2 +190 more	Copy number loss	See cases	GPathogenic
Select item 2522990	NM_181716.3(CENPV):c.803A>C (p.Asn268Thr)	CENPV (N268T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401142	NM_181716.3(CENPV):c.665A>G (p.Tyr222Cys)	CENPV (Y222C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257450	NM_181716.3(CENPV):c.652G>A (p.Val218Ile)	CENPV (V218I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478671	NM_181716.3(CENPV):c.556G>C (p.Ala186Pro)	CENPV (A186P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3142446	NM_181716.3(CENPV):c.469G>C (p.Glu157Gln)	CENPV (E157Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 736394	NM_181716.3(CENPV):c.259C>T (p.Pro87Ser)	CENPV, LOC130060319 (P87S)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2372415	NM_181716.3(CENPV):c.182C>T (p.Pro61Leu)	CENPV, LOC130060319 (P61L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396310	NM_181716.3(CENPV):c.160G>A (p.Glu54Lys)	CENPV, LOC130060319 (E54K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222213	NM_181716.3(CENPV):c.110C>T (p.Thr37Ile)	CENPV, LOC130060319 (T37I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3142443	NM_181716.3(CENPV):c.100C>G (p.Pro34Ala)	CENPV, LOC130060319 (P34A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2284177	NM_181716.3(CENPV):c.92C>T (p.Ala31Val)	CENPV, LOC130060319 (A31V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345449	NM_181716.3(CENPV):c.82G>C (p.Ala28Pro)	CENPV, LOC130060319 (A28P)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3142447	NM_181716.3(CENPV):c.74C>G (p.Ala25Gly)	CENPV, LOC130060319 (A25G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2408777	NM_181716.3(CENPV):c.74C>A (p.Ala25Glu)	CENPV, LOC130060319 (A25E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204433	NM_181716.3(CENPV):c.56G>C (p.Gly19Ala)	CENPV, LOC130060319 (G19A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3142445	NM_181716.3(CENPV):c.44A>C (p.Gln15Pro)	CENPV, LOC130060319 (Q15P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3265956	NM_181716.3(CENPV):c.18C>A (p.Ser6Arg)	CENPV, LOC130060319 (S6R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3142444	NM_181716.3(CENPV):c.17G>T (p.Ser6Ile)	CENPV, LOC130060319 (S6I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463015	NM_181716.3(CENPV):c.16A>T (p.Ser6Cys)	CENPV, LOC130060319 (S6C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2493765	NM_181716.3(CENPV):c.11C>G (p.Ser4Trp)	CENPV, LOC130060319 (S4W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3063519	GRCh37/hg19 17p11.2(chr17:16096240-16317075)x3	CENPV, NCOR1 +2 more	Copy number gain	not specified	GUncertain significance
Select item 3063517	GRCh37/hg19 17p12-11.2(chr17:15759103-20564268)x1	ADORA2B, AKAP10 +61 more	Copy number loss	not specified	GPathogenic
Select item 3063493	GRCh37/hg19 17p12-11.2(chr17:15872060-16909718)x3	ADORA2B, CCDC144A +11 more	Copy number gain	not specified	GUncertain significance
Select item 3063486	GRCh37/hg19 17p13.3-11.2(chr17:525-21510992)x3	ABR, ACADVL +329 more	Copy number gain	not specified	GPathogenic
Select item 2685597	GRCh37/hg19 17p12-11.2(chr17:15694772-20582794)x1	ADORA2B, AKAP10 +61 more	Copy number loss	not provided	GPathogenic
Select item 2684837	GRCh37/hg19 17p11.2(chr17:16193908-16490573)x3	CENPV, LRRC75A +4 more	Copy number gain	not provided	GUncertain significance
Select item 2684836	GRCh37/hg19 17p12-11.2(chr17:15633208-16567624)x3	ADORA2B, CENPV +10 more	Copy number gain	not provided	GUncertain significance
Select item 1809485	GRCh37/hg19 17p12-11.2(chr17:15754174-16657319)x3	ADORA2B, CCDC144A +10 more	Copy number gain	not provided	GUncertain significance
Select item 1808102	GRCh37/hg19 17p12-11.2(chr17:15722840-16653256)x3	ADORA2B, CCDC144A +10 more	Copy number gain	not provided	GUncertain significance
Select item 1703602	Single allele	ADORA2B, AKAP10 +78 more	Complex	PMP22-RAI1 contiguous gene duplication syndrome	GPathogenic
Select item 980122	GRCh37/hg19 17p12-11.2(chr17:15688146-16769801)x3	CENPV, LRRC75A +10 more	Copy number gain	not provided	GUncertain significance
Select item 980121	GRCh37/hg19 17p12-11.2(chr17:15688146-16756345)x1	UBB, TRPV2 +10 more	Copy number loss	not provided	GUncertain significance
Select item 980120	GRCh37/hg19 17p12-11.2(chr17:15810015-18537436)x1	ADORA2B, ALKBH5 +37 more	Copy number loss	not provided	GPathogenic
Select item 832395	NC_000017.11:g.(?_16217207)_(16972095_?)dup	CCDC144A, CENPV +7 more	Duplication	not provided	GUncertain significance
Select item 815910	GRCh37/hg19 17p12-11.2(chr17:15730101-16591260)x3	ZNF287, CENPV +9 more	Copy number gain	not provided	GUncertain significance
Select item 815909	GRCh37/hg19 17p12-11.2(chr17:15722839-16763698)x3	ZSWIM7, ADORA2B +10 more	Copy number gain	not provided	GUncertain significance
Select item 815908	GRCh37/hg19 17p12-11.2(chr17:15632431-18726389)x1	ADORA2B, ALKBH5 +42 more	Copy number loss	not provided	GPathogenic
Select item 688231	GRCh37/hg19 17p12-11.2(chr17:15722823-16796616)x3	ADORA2B, CCDC144A +10 more	Copy number gain	not provided	GUncertain significance
Select item 688172	GRCh37/hg19 17p12-11.2(chr17:15659400-16591180)x1	ADORA2B, CENPV +9 more	Copy number loss	not provided	GUncertain significance
Select item 686461	GRCh37/hg19 17p12-11.2(chr17:15599193-16756435)x3	ADORA2B, CCDC144A +12 more	Copy number gain	not provided	GUncertain significance
Select item 686350	GRCh37/hg19 17p12-11.2(chr17:15688146-16591261)x3	ADORA2B, CENPV +9 more	Copy number gain	not provided	GUncertain significance
Select item 442472	GRCh37/hg19 17p12-11.2(chr17:15688146-16727265)x3	ADORA2B, CCDC144A +10 more	Copy number gain	See cases	GLikely benign
Select item 441816	GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)x3	ALOX12, ALOX12B +1143 more	Copy number gain	See cases	GPathogenic
Select item 441815	GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)	SPEM2, TBCD +1143 more	Copy number gain	See cases	GPathogenic
Select item 394560	GRCh37/hg19 17p12-11.2(chr17:15745315-20261191)x1	ADORA2B, AKAP10 +59 more	Copy number loss	See cases	GPathogenic
Select item 253611	GRCh37/hg19 17p12-11.2(chr17:15767020-20261250)x3	ADORA2B, AKAP10 +59 more	Copy number gain	See cases	GPathogenic
Select item 221346	Single allele	ADORA2B, ADPRM +41 more	Complex	Breast ductal adenocarcinoma	GUncertain significance

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Items: 63