"ISCA site 1"[submitter] AND "LRP1B"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 148432	GRCh38/hg38 2q22.1-22.3(chr2:136937358-146681810)x1	LOC129934870, LOC129934871 +75 more	Copy number loss	See cases	GPathogenic
Select item 148593	GRCh38/hg38 2q22.1-22.2(chr2:140659197-142948096)x3	KYNU, LOC111556162 +11 more	Copy number gain	See cases	GUncertain significance
Select item 148502	GRCh38/hg38 2q22.1-22.2(chr2:140956605-141529733)x1	LOC129388925, LOC129388926 +2 more	Copy number loss	See cases	GUncertain significance
Select item 154604	GRCh38/hg38 2q22.1-22.2(chr2:141241948-142692191)x1	LOC126806360, LOC129934864 +1 more	Copy number loss	See cases	GUncertain significance
Select item 153491	GRCh38/hg38 2q22.1-22.2(chr2:141491329-142523598)x3	LOC126806360, LOC129934864 +1 more	Copy number gain	See cases	GUncertain significance
Select item 146253	GRCh38/hg38 2q22.2(chr2:141717273-142086270)x1	LRP1B	Copy number loss	See cases	GUncertain significance
Select item 442998	GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)	DCAF17, DCDC2C +1214 more	Copy number gain	See cases	GPathogenic
Select item 442997	GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)x3	AAK1, AAMP +1214 more	Copy number gain	See cases	GPathogenic
Select item 442837	GRCh37/hg19 2q22.1(chr2:139835063-141273974)x1	LRP1B	Copy number loss	See cases	GUncertain significance
Select item 441676	GRCh37/hg19 2q14.2-22.1(chr2:120571363-141627287)x1	ACMSD, AMER3 +74 more	Copy number loss	See cases	GPathogenic