MIR570HG[gene] - ClinVar

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Items: 33

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 145614	GRCh38/hg38 3q13.11-29(chr3:103426882-198110178)x3	LOC115995524, LOC115995525 +2647 more	Copy number gain	See cases	GPathogenic
Select item 57983	GRCh38/hg38 3q24-29(chr3:147521892-198096565)x3	LOC123453201, LOC123453202 +1450 more	Copy number gain	See cases	GPathogenic
Select item 150609	GRCh38/hg38 3q25.1-29(chr3:152100512-198118383)x3	LOC129938169, LOC129938170 +1318 more	Copy number gain	See cases	GPathogenic
Select item 154213	GRCh38/hg38 3q25.31-29(chr3:156118441-198125115)x3	LOC108281160, LOC108281177 +1247 more	Copy number gain	See cases	GPathogenic
Select item 152257	GRCh38/hg38 3q25.31-29(chr3:156321878-198113452)x3	ABCC5, ABCC5-AS1 +1245 more	Copy number gain	See cases	GPathogenic
Select item 57984	GRCh38/hg38 3q25.31-29(chr3:157293378-198134727)x3	LOC132088897, LOC132088898 +1201 more	Copy number gain	See cases	GPathogenic
Select item 155627	GRCh38/hg38 3q26.1-29(chr3:166137209-198125115)x3	LOC129938260, LOC129938261 +1064 more	Copy number gain	See cases	GPathogenic
Select item 148012	GRCh38/hg38 3q26.2-29(chr3:168167568-198110178)x3	LOC129938077, LOC129938078 +1041 more	Copy number gain	See cases	GPathogenic
Select item 149685	GRCh38/hg38 3q26.32-29(chr3:176168525-198118383)x3	ZMAT3, ZNF639 +867 more	Copy number gain	See cases	GPathogenic
Select item 148947	GRCh38/hg38 3q26.32-29(chr3:176439911-198118383)x3	LOC129938282, LOC129938283 +866 more	Copy number gain	See cases	GPathogenic
Select item 57868	GRCh38/hg38 3q27.2-29(chr3:185485849-198110178)x1	MIR944, MUC20 +557 more	Copy number loss	See cases	GPathogenic
Select item 57997	GRCh38/hg38 3q28-29(chr3:189265371-198110178)x3	ACAP2, APOD +411 more	Copy number gain	See cases	GPathogenic
Select item 57998	GRCh38/hg38 3q28-29(chr3:190667663-198110178)x3	LOC126806930, LOC126806931 +375 more	Copy number gain	See cases	GPathogenic
Select item 148761	GRCh38/hg38 3q29(chr3:192752937-198118383)x3	ACAP2, APOD +337 more	Copy number gain	See cases	GPathogenic
Select item 155434	GRCh38/hg38 3q29(chr3:193704605-198125115)x3	TM4SF19-DYNLT2B, TMEM44 +313 more	Copy number gain	See cases	GPathogenic
Select item 149477	GRCh38/hg38 3q29(chr3:194296197-198110198)x3	ACAP2, APOD +273 more	Copy number gain	See cases	GPathogenic
Select item 147306	GRCh38/hg38 3q29(chr3:194338534-197693741)x1	ACAP2, APOD +239 more	Copy number loss	See cases	GPathogenic
Select item 58000	GRCh38/hg38 3q29(chr3:194424496-198168758)x3	RUBCN, SENP5 +264 more	Copy number gain	See cases	GPathogenic
Select item 147389	GRCh38/hg38 3q29(chr3:195147600-195711857)x3	ACAP2, APOD +30 more	Copy number gain	See cases	GUncertain significance
Select item 149646	GRCh38/hg38 3q29(chr3:195537024-195730806)x1	APOD, LOC105374297 +12 more	Copy number loss	See cases	GLikely benign
Select item 149645	GRCh38/hg38 3q29(chr3:195537024-195730806)x3	MUC20, PPP1R2 +12 more	Copy number gain	See cases	GLikely benign
Select item 146658	GRCh38/hg38 3q29(chr3:195537179-195732718)x3	APOD, LOC105374297 +12 more	Copy number gain	See cases	GBenign
Select item 147685	GRCh38/hg38 3q29(chr3:195537187-195736631)x3	APOD, LOC105374297 +12 more	Copy number gain	See cases	GBenign
Select item 150546	GRCh38/hg38 3q29(chr3:195622114-195737540)x3	LOC105374297, MIR570 +2 more	Copy number gain	See cases	GLikely benign
Select item 151826	GRCh38/hg38 3q29(chr3:195631406-195838288)x3	LINC01983, LOC105374297 +10 more	Copy number gain	See cases	GBenign
Select item 144844	GRCh38/hg38 3q29(chr3:195631406-195699004)x4	LOC105374297, MIR570HG	Copy number gain	See cases	GBenign
Select item 144843	GRCh38/hg38 3q29(chr3:195631406-195699004)x3	LOC105374297, MIR570HG	Copy number gain	See cases	GBenign/Likely benign
Select item 152486	GRCh38/hg38 3q29(chr3:195631451-195699004)x3	LOC105374297, MIR570HG	Copy number gain	See cases	GBenign
Select item 145209	GRCh38/hg38 3q29(chr3:195654549-195699004)x3	MIR570HG	Copy number gain	See cases	GBenign/Likely benign
Select item 147029	GRCh38/hg38 3q29(chr3:195692326-195711622)x1	MIR570, MIR570HG	Copy number loss	See cases	GBenign
Select item 147028	GRCh38/hg38 3q29(chr3:195692326-195711622)x3	MIR570, MIR570HG	Copy number gain	See cases	GBenign
Select item 148016	GRCh38/hg38 3q29(chr3:195711798-198110178)x3	BDH1, CEP19 +169 more	Copy number gain	See cases	GPathogenic
Select item 59685	GRCh38/hg38 3q29(chr3:195711798-197976152)x3	LOC129938284, LOC129938285 +166 more	Copy number gain	See cases	GUncertain significance

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Items: 33