dbVar for Gene (Select 26468) - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6871210	copy number variation	1	nstd229	human		GRCh38 chr9: 122,210,976-122,211,167 , GRCh37.p13 chr9: 124,973,255-124,973,446	LHX6
nsv6870436	copy number variation	1	nstd229	human		GRCh38 chr9: 122,185,573-122,197,533 , GRCh37.p13 chr9: 124,947,852-124,959,812	LHX6, MORN5
nsv6859395	copy number variation	1	nstd229	human		GRCh38 chr9: 122,186,139-122,196,346 , GRCh37.p13 chr9: 124,948,418-124,958,625	LHX6, MORN5
nsv6637981	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 124,018,736-129,995,568 , GRCh38.p12 chr9: 121,256,458-127,233,289	PBX3-DT, ADGRD2, 119 more genes
nsv6634454	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944	HNRNPA1P41, GAS1RR, 1868 more genes
nsv6442897	copy number variation	1	nstd223	human		GRCh38 chr9: 122,185,307-122,189,620 , GRCh37.p13 chr9: 124,947,586-124,951,899	LHX6, MORN5
nsv6314001	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 116,422,275-131,713,233 , GRCh38.p12 chr9: 113,659,995-128,950,954	LOC105376244, RN7SL187P, 286 more genes
nsv6313546	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937	FAM27C, DPM2, 2166 more genes
nsv6291398	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 120,045,175-127,335,905 , GRCh38.p12 chr9: 117,282,896-124,573,626	ZBTB6, LOC105376253, 107 more genes
nsv6187096	copy number variation	1	nstd214	human		GRCh38 chr9: 122,185,431-122,185,564 , GRCh37.p13 chr9: 124,947,710-124,947,843	MORN5, LHX6
nsv6187048	copy number variation	1	nstd214	human		GRCh38 chr9: 122,185,417-122,185,549 , GRCh37.p13 chr9: 124,947,696-124,947,828	LHX6, MORN5
nsv6176497	copy number variation	1	nstd214	human		GRCh38 chr9: 122,185,148-122,185,314 , GRCh37.p13 chr9: 124,947,427-124,947,593	LHX6, MORN5
nsv6137052	copy number variation	1	nstd213	human		GRCh37 chr9: 123,200,000-125,840,001 , GRCh38.p12 chr9: 120,437,722-123,077,722	MEGF9, GGTA1, 61 more genes
nsv6014056	copy number variation	1	nstd212	human		GRCh38 chr9: 122,185,424-122,185,559 , GRCh37.p13 chr9: 124,947,703-124,947,838	MORN5, LHX6
nsv5924292	copy number variation	1	nstd209	human		GRCh38 chr9: 122,185,417-122,185,549 , GRCh37.p13 chr9: 124,947,696-124,947,828	LHX6, MORN5
nsv5640866	insertion	1	nstd207	human		GRCh38 chr9: 122,191,048-122,191,048 , GRCh37.p13 chr9: 124,953,327-124,953,327	LHX6, MORN5
nsv5634759	insertion	1	nstd207	human		GRCh38 chr9: 122,185,417-122,185,417 , GRCh37.p13 chr9: 124,947,696-124,947,696	LHX6, MORN5
nsv5631269	insertion	1	nstd207	human		GRCh38 chr9: 122,189,561-122,189,561 , GRCh37.p13 chr9: 124,951,840-124,951,840	LHX6, MORN5
nsv5604518	copy number variation	1	nstd207	human		GRCh38 chr9: 122,185,417-122,185,549 , GRCh37.p13 chr9: 124,947,696-124,947,828	LHX6, MORN5
nsv5476659	copy number variation	1	nstd206	human		GRCh38 chr9: 122,229,067-122,229,261 , GRCh37.p13 chr9: 124,991,346-124,991,540	LHX6

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 150

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Number of Variants: 20

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