ClinVar for Gene (Select 10156) - ClinVar

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Links from Gene

Items: 28

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685259	GRCh37/hg19 7q22.1(chr7:102138955-102744237)x1	NFE4, POLR2J2 +11 more	Copy number loss	not provided	GUncertain significance
Select item 2657886	NM_006989.6(RASA4):c.834C>T (p.His278=)	RASA4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2373150	NM_006989.6(RASA4):c.1001G>T (p.Arg334Leu)	RASA4 (R334L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356682	NM_006989.6(RASA4):c.946G>A (p.Gly316Arg)	RASA4 (G316R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343710	NM_006989.6(RASA4):c.331G>A (p.Asp111Asn)	RASA4 (D111N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2247386	NM_006989.6(RASA4):c.1001G>C (p.Arg334Pro)	RASA4 (R334P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1808822	GRCh37/hg19 7q22.1(chr7:102101275-102406667)x1	ALKBH4, FAM185A +9 more	Copy number loss	not provided	GUncertain significance
Select item 1708459	GRCh37/hg19 7p22.3-q36.3(chr7:56604613-96692931)x1	AASS, ABCA13 +896 more	Copy number loss	See cases	GUncertain significance
Select item 1703560	Single allele	CACNA2D1, CADPS2 +896 more	Complex	Ring chromosome 7	GPathogenic
Select item 1527380	GRCh37/hg19 7q22.1-31.31(chr7:100676872-119156160)	ALKBH4, ANKRD7 +95 more	Copy number loss	not specified	GPathogenic
Select item 1527379	GRCh37/hg19 7q22.1-31.1(chr7:99417471-111586308)	ACHE, ACTL6B +123 more	Copy number loss	not specified	GPathogenic
Select item 1252701	NM_006989.6(RASA4):c.339T>C (p.Asp113=)	RASA4	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1224860	NM_006989.6(RASA4):c.422A>G (p.Glu141Gly)	RASA4 (E141G)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 929826	GRCh37/hg19 7q22.1(chr7:99593346-102470275)x1	ACHE, ACTL6B +77 more	Copy number loss	See cases	GLikely pathogenic
Select item 687427	GRCh37/hg19 7p22.3-q36.3(chr7:10365-159119707)x3	PRSS1, PRSS37 +896 more	Copy number gain	not provided	GPathogenic
Select item 563422	GRCh37/hg19 7q22.1-36.3(chr7:98693388-159119707)x3	AASS, ABCB8 +436 more	Copy number gain	not provided	GPathogenic
Select item 563415	GRCh37/hg19 7q22.1(chr7:98847725-102472176)x1	CYP3A43, GJC3 +99 more	Copy number loss	not provided	GPathogenic
Select item 442834	GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707)x3	AVL9, AZGP1 +896 more	Copy number gain	See cases	GPathogenic
Select item 442833	GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707)	MCM7, MDFIC +896 more	Copy number gain	See cases	GPathogenic
Select item 402244	TMEM106B-BRAF fusion	AASS, ABCA13 +678 more	Deletion	Pleomorphic xanthoastrocytoma	GPathogenic
Select item 242972	NC_000007.13:g.(20954043_21001537)_(114528369_114556605)inv	ARMC10, ASB4 +504 more	Inversion	Childhood apraxia of speech	GPathogenic
Select item 154898	GRCh38/hg38 7q22.1(chr7:102514724-102643741)x3	POLR2J2-UPK3BL1, POLR2J3 +6 more	Copy number gain	See cases	GLikely benign
Select item 150163	GRCh38/hg38 7q22.1(chr7:102514724-102692431)x3	POLR2J2, POLR2J2-UPK3BL1 +8 more	Copy number gain	See cases	GLikely benign
Select item 148448	GRCh38/hg38 7q22.1-31.31(chr7:102196924-121278641)x1	ALKBH4, ANKRD7 +474 more	Copy number loss	See cases	GPathogenic
Select item 147547	GRCh38/hg38 7q21.3-36.3(chr7:97419852-158923762)x3	LOC123956257, LOC123956258 +2213 more	Copy number gain	See cases	GPathogenic
Select item 146075	GRCh38/hg38 7p22.3-q36.3(chr7:54185-159282390)x1	CUL1, CUX1 +4737 more	Copy number loss	See cases	GPathogenic
Select item 57255	GRCh38/hg38 7q22.1-31.1(chr7:101807149-112414850)x1	ALKBH4, ARMC10 +292 more	Copy number loss	See cases	GPathogenic
Select item 57092	GRCh38/hg38 7q22.1-22.3(chr7:101525795-105432462)x3	ALKBH4, ARMC10 +149 more	Copy number gain	See cases	GPathogenic

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Links from Gene

Items: 28