ecd[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
nsv3898940	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 96,112,693-96,117,336 , GRCh38.p12 chr7: 96,483,381-96,488,024	LOC105375411, SEM1
nsv3894477	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 96,116,424-96,118,498 , GRCh38.p12 chr7: 96,487,112-96,489,186	LOC105375411, SEM1
nsv3904262	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 96,049,191-96,208,580 , GRCh38.p12 chr7: 96,419,879-96,579,268	SEM1, LOC105375411, 3 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	RNU6-438P, LOC105375300, 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	LOC107986817, DNAJB9, 2014 more genes
nsv7137209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639	ECD, RNU7-12P, 1876 more genes
nsv3922335	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 60,196,226-76,174,974 , GRCh38 chr10: 58,436,466-74,415,216 , NCBI36 chr10: 59,866,232-75,844,980	ECD, UNC5B-AS1, 250 more genes
nsv3917822	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 63,402,579-75,296,099 , GRCh37 chr10: 65,162,339-77,055,857 , NCBI36 chr10: 64,832,345-76,725,863	ECD, MYL6P3, 220 more genes
nsv6314185	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 68,735,254-78,885,714 , GRCh38.p12 chr10: 66,975,496-77,125,956	ECD, SLC25A16, 204 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	LOC105375402, LOC112267858, 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	MARK2P10, PON2, 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	LOC105375410, LOC107984034, 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	LOC105375404, LOC107984034, 52 more genes
nsv3908984	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 93,285,237-96,280,817 , GRCh38.p12 chr7: 93,655,925-96,651,505	LOC105375402, PPP1R9A-AS1, 51 more genes
nsv3910545	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 74,150,392-77,042,138 , GRCh38 chr10: 72,720,628-75,612,374 , GRCh37 chr10: 74,480,386-77,372,132	ECD, CAMK2G, 73 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	RNU6-532P, DLX6-AS1, 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	DYNC1I1, DLX6-AS1, 18 more genes
nsv6636425	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 95,258,682-96,465,856 , GRCh38.p12 chr7: 95,629,370-96,836,544	RNU7-188P, RNU6-364P, 14 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	SDHAF3, DLX6, 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	RNU6-565P, LAMB1, 2684 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 41

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Number of Variants: 20

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Supplemental Content

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