dbVar for OMIM (Select 133701) - dbVar - NCBI

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Items: 16

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Number of Variants: 16

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6309215	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 44,219,359-44,228,529 , GRCh38.p12 chr11: 44,197,809-44,206,979	EXT2
nsv6309214	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 44,129,235-44,129,808 , GRCh38.p12 chr11: 44,107,685-44,108,258	EXT2
nsv6309111	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 44,129,235-44,151,698 , GRCh38.p12 chr11: 44,107,685-44,130,148	EXT2
nsv6308939	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 44,109,277-44,109,441 , GRCh37 chr11: 44,130,827-44,130,991	EXT2
nsv4683778	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 44,117,783-44,151,708 , GRCh38.p12 chr11: 44,096,233-44,130,158	EXT2
nsv4682485	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 44,129,213-44,129,818 , GRCh38.p12 chr11: 44,107,663-44,108,268	EXT2
nsv4681665	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 44,146,319-44,148,525 , GRCh38.p12 chr11: 44,124,769-44,126,975	EXT2
nsv4681231	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 44,193,141-44,228,529 , GRCh38.p12 chr11: 44,171,591-44,206,979	EXT2
nsv4681130	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 44,117,783-44,265,938 , GRCh38.p12 chr11: 44,096,233-44,244,388	EXT2
nsv4453361	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 44,124,906-44,135,425 , GRCh37.p13 chr11: 44,146,456-44,156,975	EXT2
nsv3889783	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 44,228,323-44,228,529 , GRCh38 chr11: 44,206,773-44,206,979	EXT2
nsv3884709	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 44,193,141-44,193,312 , GRCh38 chr11: 44,171,591-44,171,762	EXT2
nsv3874010	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 44,228,343-44,228,509 , GRCh38 chr11: 44,206,793-44,206,959	EXT2
nsv3872432	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 44,144,227-44,198,038 , GRCh37 chr11: 44,165,777-44,219,588	EXT2
nsv3871801	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 44,107,663-44,130,158 , GRCh37 chr11: 44,129,213-44,151,708	EXT2
nsv997192	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chr11: 44,117,099-44,266,980 , GRCh38.p12 chr11: 44,095,549-44,245,430	EXT2

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dbVar for OMIM (Select 133701) (18)
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