esv20995 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
esv29172	sequence alteration	4	estd20	human		NCBI36 chr2: 230,781,222-231,176,091 , GRCh37.p13 chr2: 231,072,978-231,467,847 , GRCh38.p12 chr2: 230,208,263-230,603,132	SP110, LOC101928816, 9 more genes
esv20995	copy number variation	1	estd20	human		NCBI36 chr2: 231,138,003-231,138,630 , GRCh37.p13 chr2: 231,429,759-231,430,386 , GRCh38.p12 chr2: 230,565,044-230,565,671	0