dbVar for Gene (Select 7763) - 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
nsv5856410	copy number variation	1	nstd209	human		GRCh38 chr9: 72,349,264-72,350,363 , GRCh37.p13 chr9: 74,964,180-74,965,279	ZFAND5
nsv4968364	copy number variation	1	nstd200	human		GRCh38 chr9: 72,356,152-72,356,330 , GRCh37.p13 chr9: 74,971,068-74,971,246	ZFAND5
nsv4968363	copy number variation	1	nstd200	human		GRCh38 chr9: 72,352,836-72,354,344 , GRCh37.p13 chr9: 74,967,752-74,969,260	ZFAND5
nsv4814043	copy number variation	1	nstd200	human		GRCh37 chr9: 74,967,752-74,969,260 , GRCh38.p12 chr9: 72,352,836-72,354,344	ZFAND5
nsv4728828	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 74,173,350-75,170,163 , GRCh38.p12 chr9: 71,558,434-72,555,247	LOC100289320, TMC1, 16 more genes
nsv4679980	copy number variation	1	nstd189	human		GRCh37.p13 chr9: 74,891,446-75,224,013 , GRCh38.p12 chr9: 72,276,530-72,609,097	ZFAND5, TMC1, 6 more genes
nsv4604654	copy number variation	1	nstd183	human		GRCh37 chr9: 74,975,116-74,984,763 , GRCh38.p12 chr9: 72,360,200-72,369,847	ZFAND5
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
nsv4181076	copy number variation	1	nstd166	human		GRCh37.p13 chr9: 74,977,482-74,978,799 , GRCh38.p12 chr9: 72,362,566-72,363,883	ZFAND5
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
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
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
nsv3916525	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 72,023,067-72,497,412 , GRCh37 chr9: 74,637,983-75,112,328 , NCBI36 chr9: 73,827,803-74,302,148	LOC100289351, C9orf57, 8 more genes

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Items: 1 to 20 of 149

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Number of Variants: 20

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