dbVar for OMIM (Select 238331) - dbVar - NCBI

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Items: 3

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Number of Variants: 3

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7097603	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 107,412,489-107,559,714 , GRCh38.p12 chr7: 107,772,044-107,919,269	LOC105375444, DLD, 3 more genes
nsv6312606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 107,556,049-107,558,012 , GRCh38.p12 chr7: 107,915,604-107,917,567	DLD
nsv4682811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 107,542,173-107,546,823 , GRCh38.p12 chr7: 107,901,728-107,906,378	DLD

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dbVar for OMIM (Select 238331) (4)
dbVar
Sargocentron sp. mixed lineage leukemia-like protein (Mll) gene, partial cds
Sargocentron sp. mixed lineage leukemia-like protein (Mll) gene, partial cds
gi|5833326|gb|AF137240.1|

Nucleotide
Homo sapiens uncharacterized LOC100506124 (LOC100506124), long non-coding RNA
Homo sapiens uncharacterized LOC100506124 (LOC100506124), long non-coding RNA
gi|920816792|ref|NR_045375.2|

Nucleotide

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