dbVar for Gene (Select 653162) - 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
nsv5480328	copy number variation	1	nstd206	human		GRCh38 chr9: 76,398,626-76,398,690 , GRCh37.p13 chr9: 79,013,542-79,013,606	RPSAP9
nsv4552239	insertion	1	nstd166	human		GRCh37.p13 chr9: 79,013,159-79,013,159 , GRCh38.p12 chr9: 76,398,243-76,398,243	RPSAP9
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
nsv4456241	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 78,787,760-79,180,790 , GRCh38.p12 chr9: 76,172,844-76,565,874	RBM22P5, GCNT1, 6 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
nsv4191004	copy number variation	1	nstd166	human		GRCh37.p13 chr9: 79,010,888-79,019,199 , GRCh38.p12 chr9: 76,395,972-76,404,283	RPSAP9
nsv3924278	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr9: 76,127,281-76,968,483 , NCBI36 chr9: 77,932,017-78,773,219 , GRCh37 chr9: 78,742,197-79,583,399	GCNT1, LOC105376093, 10 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
nsv3915966	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr9: 77,978,209-78,371,220 , GRCh37.p13 chr9: 78,788,389-79,181,400 , GRCh38.p12 chr9: 76,173,473-76,566,484	RBM22P5, GCNT1, 6 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

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Has Clinical Interpretation

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Items: 1 to 20 of 106

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Number of Variants: 20

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