dbVar for OMIM (Select 614436) - dbVar - NCBI

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Items: 17

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Number of Variants: 17

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7098422	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr9: 130,241,728-130,244,069 , GRCh38.p12 chr9: 127,479,449-127,481,790	LRSAM1
nsv7098055	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr9: 130,248,084-130,254,631 , GRCh38.p12 chr9: 127,485,805-127,492,352	LRSAM1
nsv7098054	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 130,245,209-130,245,319 , GRCh38.p12 chr9: 127,482,930-127,483,040	LRSAM1
nsv7098053	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 130,229,999-130,230,129 , GRCh38.p12 chr9: 127,467,720-127,467,850	LRSAM1
nsv7097687	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 130,221,262-130,224,672 , GRCh38.p12 chr9: 127,458,983-127,462,393	LRSAM1
nsv6314300	insertion	1	nstd102	human	Uncertain significance	GRCh38 chr9: 127,455,636-127,455,636 , GRCh37 chr9: 130,217,915-130,217,915	LRSAM1
nsv6313249	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 130,216,807-130,265,178 , GRCh38.p12 chr9: 127,454,528-127,502,899	LRSAM1
nsv6312750	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 130,265,033-130,265,178 , GRCh38.p12 chr9: 127,502,754-127,502,899	LRSAM1
nsv6312749	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 130,216,797-130,224,662 , GRCh38.p12 chr9: 127,454,518-127,462,383	LRSAM1
nsv6312666	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr9: 130,242,098-130,242,160 , GRCh38 chr9: 127,479,819-127,479,881	LRSAM1
nsv4683869	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 130,223,442-130,236,220 , GRCh38.p12 chr9: 127,461,163-127,473,941	LRSAM1
nsv4683261	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr9: 130,265,043-130,265,188 , GRCh38.p12 chr9: 127,502,764-127,502,909	LRSAM1
nsv4682914	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 130,216,797-130,265,188 , GRCh38.p12 chr9: 127,454,518-127,502,909	LRSAM1
nsv4454380	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr9: 130,241,728-130,244,069 , GRCh38 chr9: 127,479,449-127,481,790	LRSAM1
nsv4449900	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 127,501,000-127,501,153 , GRCh37 chr9: 130,263,279-130,263,432	LRSAM1
nsv3881934	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr9: 130,264,298-130,265,271 , GRCh38 chr9: 127,502,019-127,502,992	LRSAM1
nsv3880744	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 130,265,053-130,265,780 , GRCh38 chr9: 127,502,774-127,503,501	NIBAN2, LRSAM1

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