dbVar for Gene (Select 100286938) - 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
nsv4728915	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 79,706,373-79,971,001 , GRCh38.p12 chr9: 77,091,457-77,356,085	VPS13A-AS1, VPS13A
nsv4605260	copy number variation	1	nstd183	human		GRCh37 chr9: 79,770,637-79,792,552 , GRCh38.p12 chr9: 77,155,721-77,177,636	VPS13A-AS1, VPS13A
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
nsv4455073	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 78,672,613-83,349,616 , GRCh38.p12 chr9: 76,057,697-80,734,701	LOC105376100, NPAP1P6, 49 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
nsv4424474	copy number variation	1	nstd174	human		GRCh37 chr9: 79,763,087-79,795,677 , GRCh38.p12 chr9: 77,148,171-77,180,761	VPS13A, VPS13A-AS1
nsv4349215	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 79,520,825-97,201,274 , GRCh38.p12 chr9: 76,905,909-94,438,992	SPATA31C1, LINC02893, 280 more genes
nsv3923526	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 74,029,084-79,136,863 , GRCh37 chr9: 74,839,264-79,947,043 , GRCh38 chr9: 72,224,348-77,332,127	GCNT1, NMRK1, 65 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
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
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
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
nsv3913696	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr9: 78,801,475-79,219,782 , GRCh37 chr9: 79,611,655-80,029,962 , GRCh38 chr9: 76,996,739-77,415,046	VPS13A-AS1, LOC105376096, 4 more genes
nsv3913411	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 75,511,422-82,175,364 , GRCh37 chr9: 76,321,602-82,985,544 , GRCh38 chr9: 73,706,686-80,370,629	OTX2P1, RPSAP9, 72 more genes

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Number of Variants: 20

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