dlx5[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
nsv3919858	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 96,391,401-96,624,516 , GRCh37 chr7: 96,553,465-96,786,580 , GRCh38 chr7: 96,924,153-97,157,268	DLX5, DLX6, 5 more genes
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	DLX5, 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	DLX5, LOC107986817, 2014 more genes
nsv3892887	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 92,445,452-99,686,985 , GRCh38.p12 chr7: 92,816,138-100,089,362	DLX5, LOC105375402, 153 more genes
nsv6636271	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 92,721,627-98,311,537 , GRCh38.p12 chr7: 93,092,314-98,682,225	DLX5, MARK2P10, 97 more genes
nsv3911538	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 92,226,394-97,035,894 , GRCh38 chr7: 92,759,144-97,568,646 , GRCh37 chr7: 92,388,458-97,197,958	DLX5, LOC105375410, 75 more genes
nsv3901032	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 93,700,162-96,950,914 , GRCh38.p12 chr7: 94,070,850-97,321,602	DLX5, LOC105375404, 52 more genes
nsv3922980	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 94,756,382-97,502,799 , GRCh38 chr7: 95,127,070-97,873,487 , NCBI36 chr7: 94,594,318-97,340,735	DLX5, RNU6-532P, 41 more genes
nsv6312877	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 95,434,042-96,747,209 , GRCh38.p12 chr7: 95,804,730-97,117,897	DLX5, DYNC1I1, 18 more genes
nsv6636511	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 96,264,152-96,860,892 , GRCh38.p12 chr7: 96,634,840-97,231,580	DLX5, SDHAF3, 9 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	DLX5, 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	DLX5, 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	DLX5, 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	DLX5, TRGV3, 2682 more genes
nsv5381780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 87,477,185-100,333,327 , GRCh38.p12 chr7: 87,847,870-100,735,704	DLX5, ARPC1A, 265 more genes
nsv6315223	complex substitution	1	nstd102	human	Pathogenic	GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017	DLX5, 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	DLX5, ACHE, 1532 more genes
nsv4685991	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr7: 95,911,538-97,301,820 , GRCh38.p12 chr7: 96,282,226-97,672,508	DLX5, DLX6, 22 more genes
nsv6634332	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635	DLX5, RRBP1P1, 2680 more genes
nsv3899656	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 96,066,104-97,428,089 , GRCh38.p12 chr7: 96,436,792-97,798,777	DLX5, LOC107984034, 18 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 21

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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