ClinVar for Gene (Select 924) - ClinVar

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Links from Gene

Items: 47

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3264869	NM_006137.7(CD7):c.460G>A (p.Ala154Thr)	CD7 (A154T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3243134	NC_000017.10:g.(?_79477716)_(80901020_?)dup	ACTG1, ALYREF +52 more	Duplication	not provided	GUncertain significance
Select item 3242977	NC_000017.10:g.(?_80039865)_(80901020_?)dup	CCDC57, CD7 +18 more	Duplication	Epileptic encephalopathy	GUncertain significance
Select item 3140656	NM_006137.7(CD7):c.685C>A (p.Arg229Ser)	CD7 (R229S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140655	NM_006137.7(CD7):c.618G>C (p.Lys206Asn)	CD7 (K206N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140654	NM_006137.7(CD7):c.464C>T (p.Pro155Leu)	CD7 (P155L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2671602	Single allele	ASPSCR1, B3GNTL1 +28 more	Duplication	not provided	GUncertain significance
Select item 2606103	NM_006137.7(CD7):c.281A>G (p.Gln94Arg)	CD7 (Q94R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590760	NM_006137.7(CD7):c.577G>A (p.Gly193Ser)	CD7 (G193S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554400	NM_006137.7(CD7):c.56G>T (p.Gly19Val)	CD7 (G19V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535716	NM_006137.7(CD7):c.329G>A (p.Gly110Asp)	CD7 (G110D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521121	NM_006137.7(CD7):c.476C>T (p.Ser159Phe)	CD7 (S159F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516972	NM_006137.7(CD7):c.260G>A (p.Arg87His)	CD7 (R87H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516851	NM_006137.7(CD7):c.308G>A (p.Arg103His)	CD7 (R103H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2499662	GRCh38/hg38 17q25.3(chr17:82004063-83087346)	ASPSCR1, B3GNTL1 +130 more	Copy number loss	Anomalous pulmonary venous return	GUncertain significance
Select item 2488938	NM_006137.7(CD7):c.644A>G (p.Asn215Ser)	CD7 (N215S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2445210	Single allele	FOXK2, GCGR +51 more	Deletion	See cases	GPathogenic
Select item 2425655	NC_000017.10:g.(?_79891090)_(80333370_?)del	ASPSCR1, CCDC57 +17 more	Deletion	not provided	GPathogenic
Select item 2424500	NC_000017.10:g.(?_79477716)_(80900339_?)dup	ACTG1, ALYREF +52 more	Duplication	not provided	GUncertain significance
Select item 2387364	NM_006137.7(CD7):c.370G>A (p.Gly124Ser)	CD7 (G124S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357629	NM_006137.7(CD7):c.243C>A (p.Asp81Glu)	CD7 (D81E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286477	NM_006137.7(CD7):c.10C>G (p.Pro4Ala)	CD7 (P4A)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2275757	NM_006137.7(CD7):c.136A>G (p.Ile46Val)	CD7 (I46V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255493	NM_006137.7(CD7):c.14C>T (p.Pro5Leu)	CD7 (P5L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211590	NM_006137.7(CD7):c.635G>A (p.Arg212Gln)	CD7 (R212Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1701331	GRCh37/hg19 17q25.1-25.3(chr17:73481509-81043199)x3	EVPL, EXOC7 +146 more	Copy number gain	not provided	GPathogenic
Select item 1526589	GRCh37/hg19 17q25.3(chr17:79976464-81041938)	B3GNTL1, CCDC57 +27 more	Copy number loss	not specified	GUncertain significance
Select item 689209	GRCh37/hg19 17q24.1-25.3(chr17:62778720-81041938)x3	AANAT, AATK +226 more	Copy number gain	not provided	GPathogenic
Select item 687727	GRCh37/hg19 17q25.3(chr17:78608912-81041938)x3	AATK, ACTG1 +65 more	Copy number gain	not provided	GPathogenic
Select item 564478	GRCh37/hg19 17q25.3(chr17:80243845-80374899)x1	SECTM1, UTS2R +3 more	Copy number loss	not provided	GLikely benign
Select item 564476	GRCh37/hg19 17q25.3(chr17:76552611-81041938)x3	AATK, ACTG1 +88 more	Copy number gain	not provided	GLikely pathogenic
Select item 564463	GRCh37/hg19 17q24.1-25.3(chr17:63689671-81041938)x3	AANAT, AATK +222 more	Copy number gain	not provided	GPathogenic
Select item 443488	GRCh37/hg19 17q24.2-25.3(chr17:67002415-81041938)x3	AANAT, AATK +202 more	Copy number gain	See cases	GPathogenic
Select item 443446	GRCh37/hg19 17q25.1-25.3(chr17:73951701-81041938)x3	AANAT, AATK +128 more	Copy number gain	See cases	GPathogenic
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 395646	GRCh37/hg19 17q21.31-25.3(chr17:42580684-81085615)x3	AANAT, AATK +458 more	Copy number gain	See cases	GPathogenic
Select item 155275	GRCh38/hg38 17q24.3-25.3(chr17:69916435-83102552)x3	AANAT, AATK +1013 more	Copy number gain	See cases	GPathogenic
Select item 153720	GRCh38/hg38 17q25.3(chr17:81401966-83084062)x1	ACTG1, ALYREF +226 more	Copy number loss	See cases	GLikely pathogenic
Select item 149717	GRCh38/hg38 17q25.3(chr17:81008196-83102584)x3	AATK, ACTG1 +262 more	Copy number gain	See cases	GPathogenic
Select item 148281	GRCh38/hg38 17q25.3(chr17:82072338-83102552)x1	LOC130062052, LOC130062053 +112 more	Copy number loss	See cases	GLikely pathogenic
Select item 60176	GRCh38/hg38 17q25.3(chr17:82078456-82568008)x3	CCDC57, CD7 +73 more	Copy number gain	See cases	GUncertain significance
Select item 60175	GRCh38/hg38 17q25.3(chr17:81885863-82358856)x3	LOC130062008, LOC130062009 +95 more	Copy number gain	See cases	GUncertain significance
Select item 58714	GRCh38/hg38 17q25.3(chr17:78918650-83021095)x3	AATK, ACTG1 +385 more	Copy number gain	See cases	GPathogenic
Select item 58703	GRCh38/hg38 17q24.3-25.3(chr17:69209079-83086677)x3	MIR636, MIR6516 +1033 more	Copy number gain	See cases	GPathogenic
Select item 57263	GRCh38/hg38 17q25.3(chr17:78901959-83086677)x3	AATK, ACTG1 +387 more	Copy number gain	See cases	GPathogenic
Select item 57076	GRCh38/hg38 17q25.3(chr17:78092236-83086677)x3	AATK, ACTG1 +513 more	Copy number gain	See cases	GPathogenic

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Links from Gene

Items: 47