dbVar for OMIM (Select 303100) - dbVar

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Links from OMIM

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7137164	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chrX: 85,166,265-85,166,342 , GRCh38 chrX: 85,911,260-85,911,337	CHM
nsv5381815	inversion	1	nstd102	human	Pathogenic	GRCh37 chrX: 85,296,960-85,303,374 , GRCh38 chrX: 86,041,956-86,048,370	CHM
nsv997151	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chrX: 85,116,185-85,302,569 , GRCh38.p12 chrX: 85,861,180-86,047,565	CHM, MIR361