dbVar for Gene (Select 406987) - 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
nsv4679000	copy number variation	1	nstd189	human		GRCh37.p13 chr9: 73,419,492-73,912,696 , GRCh38.p12 chr9: 70,804,576-71,297,780	TRPM3, MIR204, 3 more genes
nsv4457273	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936	CDRT15P14, MIR548AW, 2167 more genes
nsv4455928	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 70,974,661-81,829,792 , GRCh38.p12 chr9: 68,359,745-79,214,877	RPL35AP21, LOC105376097, 134 more genes
nsv4455186	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937	LOC105376327, ENG, 1304 more genes
nsv4436161	complex substitution	1	nstd102	human	Likely pathogenic	GRCh38.p12 chr9: 23,524,428-84,744,973 , GRCh37 chr9: 23,524,426-87,359,888	ACO1, ALDH1A1, 779 more genes
nsv3923489	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr9: 71,455,395-73,762,803 , GRCh37.p13 chr9: 72,265,575-74,572,983 , GRCh38.p12 chr9: 69,650,659-71,958,067	LOC105376079, PIGUP1, 26 more genes
nsv3922915	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 73,012,899-74,599,032 , GRCh38 chr9: 70,397,983-71,984,116 , NCBI36 chr9: 72,202,719-73,788,852	LOC105376079, PIGUP1, 14 more genes
nsv3922684	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897	TDRD7, CDK9, 2170 more genes
nsv3921598	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 203,861-138,125,937 , NCBI36 chr9: 193,861-140,140,210 , GRCh37 chr9: 203,861-141,020,389	PGAP4, ECPAS, 2167 more genes
nsv3920777	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 70,259,583-78,057,599 , GRCh38 chr9: 68,454,847-76,252,863 , GRCh37 chr9: 71,130,848-78,867,779	ANXA1, LOC105376080, 96 more genes
nsv3920713	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 193,862-140,140,210 , GRCh38 chr9: 203,862-138,125,937 , GRCh37 chr9: 203,862-141,020,389	ABHD17B, LOC100533707, 2167 more genes
nsv3919257	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 204,193-141,073,897 , GRCh38 chr9: 204,193-138,179,445 , NCBI36 chr9: 194,193-140,193,718	LOC107987031, LOC105376234, 2169 more genes
nsv3918139	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr9: 70,429,219-73,833,573 , GRCh37 chr9: 71,239,399-74,643,753 , GRCh38 chr9: 68,624,483-72,028,837	APBA1, KLF9, 40 more genes
nsv3917022	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 214,367-141,008,915 , GRCh38 chr9: 193,412-138,114,463 , NCBI36 chr9: 204,367-140,128,736	RN7SKP87, SPATA6L, 2168 more genes
nsv3915973	copy number variation	2	nstd102	human	Pathogenic	GRCh38 chr9: 193,412-138,159,073 , GRCh37 chr9: 68,420,641-141,053,525 , NCBI36 chr9: 67,910,461-140,173,346	CTNNAL1, QSOX2, 2170 more genes
nsv3915174	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 70,304,266-85,474,962 , GRCh38 chr9: 68,499,530-83,670,227 , GRCh37 chr9: 71,130,848-86,285,142	LOC107987086, PGM5, 183 more genes
nsv3915095	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 193,412-74,615,913 , NCBI36 chr9: 194,193-76,420,649 , GRCh37 chr9: 204,193-77,230,829	MTCO3P36, BMS1P14, 934 more genes
nsv3914702	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 71,130,848-109,341,774 , NCBI36 chr9: 70,225,166-108,381,595 , GRCh38 chr9: 68,420,430-106,579,493	CDCA7P2, ASPN, 603 more genes
nsv3912576	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 194,104-81,682,551 , GRCh37 chr9: 204,104-82,492,731 , GRCh38 chr9: 193,412-79,877,816	CDK2AP2P1, TRBV21OR9-2, 996 more genes
nsv3912247	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 2,934-140,273,252 , GRCh37.p13 chr9: 12,934-141,153,431 , GRCh38.p12 chr9: 12,934-138,262,981	ALOX15P2, LOC107987061, 2184 more genes

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Number of Variants: 20

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Has Clinical Interpretation

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Items: 1 to 20 of 88

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Number of Variants: 20

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