esv13033 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
esv27425	sequence alteration	1	estd20	human		NCBI36 chr2: 105,028,475-105,031,989 , GRCh37.p13 chr2: 105,662,043-105,665,557 , GRCh38.p12 chr2: 105,045,585-105,049,099	MRPS9
esv13033	copy number variation	1	estd20	human		NCBI36 chr2: 105,028,475-105,031,989 , GRCh37.p13 chr2: 105,662,043-105,665,557 , GRCh38.p12 chr2: 105,045,585-105,049,099	MRPS9