avl9[All Fields] AND 1[has_clinical] - 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
nsv3907598	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 32,549,976-32,550,976 , GRCh38.p12 chr7: 32,510,364-32,511,364	AVL9
nsv3919826	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840	AVL9, RNU6-438P, 2682 more genes
nsv3888815	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467	AVL9, LOC107986817, 2014 more genes
nsv3892894	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 22,935,369-32,621,975 , GRCh38.p12 chr7: 22,895,750-32,582,363	AVL9, NPVF, 168 more genes
nsv4674822	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 23,877,135-33,139,446 , GRCh38.p12 chr7: 23,837,516-33,099,834	AVL9, RP9P, 156 more genes
nsv6315453	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 25,451,740-33,864,069 , GRCh38.p12 chr7: 25,412,121-33,824,457	AVL9, PLEKHA8, 141 more genes
nsv6636445	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 27,133,786-34,466,477 , GRCh38.p12 chr7: 27,094,167-34,426,865	AVL9, MIR550A1, 119 more genes
nsv3894780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842	AVL9, RNU6-565P, 2684 more genes
nsv4455091	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017	AVL9, RPL23AP51, 2684 more genes
nsv3909087	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 44,935-159,126,310 , GRCh38.p12 chr7: 44,935-159,333,620	AVL9, MNX1-AS2, 2682 more genes
nsv3908592	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr7: 43,361-159,119,707 , GRCh38.p12 chr7: 43,361-159,327,017	AVL9, TRGV3, 2682 more genes
nsv3915802	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-41,915,483 , GRCh38 chr7: 54,185-41,875,885 , NCBI36 chr7: 149,268-41,882,008	AVL9, RPL23AP52, 638 more genes
nsv3899194	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 11,048,840-52,863,626 , GRCh38.p12 chr7: 11,009,213-52,795,933	AVL9, BRWD1P3, 590 more genes
nsv3918785	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-37,129,317 , NCBI36 chr7: 149,268-37,095,842 , GRCh38 chr7: 54,185-37,089,712	AVL9, MMD2, 554 more genes
nsv3895449	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 11,562,624-36,395,416 , GRCh38.p12 chr7: 11,522,997-36,355,807	AVL9, HOXA7, 343 more genes
nsv3898448	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 30,463,886-43,470,805 , GRCh38.p12 chr7: 30,424,270-43,431,206	AVL9, INMT, 193 more genes
nsv3917886	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 30,427,074-34,566,802 , GRCh38 chr7: 30,420,933-34,560,665 , GRCh37 chr7: 30,460,549-34,600,277	AVL9, INMT, 48 more genes
nsv6315223	complex substitution	1	nstd102	human	Pathogenic	GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017	AVL9, AOC1, 2682 more genes
nsv4352523	inversion	1	nstd102	human	Pathogenic	GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550	AVL9, ACHE, 1532 more genes
nsv3921383	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr7: 30,944,510-33,407,133 , GRCh37 chr7: 30,977,985-33,440,608 , GRCh38 chr7: 30,938,370-33,400,996	AVL9, ADCYAP1R1, 31 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 24

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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