garem1[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
nsv3893977	copy number variation	1	nstd102	human	Benign	GRCh37 chr18: 29,885,871-29,889,203 , GRCh38.p12 chr18: 32,305,908-32,309,240	GAREM1
nsv3891912	copy number variation	1	nstd102	human	Benign	GRCh37 chr18: 29,888,503-29,890,042 , GRCh38.p12 chr18: 32,308,540-32,310,079	GAREM1
nsv6314722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 1,262,334-53,254,751 , GRCh38.p12 chr18: 1,262,333-55,587,520	GAREM1, LOC107985176, 632 more genes
nsv3900710	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 20,069,932-36,887,326 , GRCh38.p12 chr18: 22,489,969-39,307,362	GAREM1, CABLES1, 174 more genes
nsv3912224	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 27,945,491-39,904,182 , GRCh38 chr18: 32,111,530-44,070,219 , GRCh37 chr18: 29,691,493-41,650,184	GAREM1, SYT4, 94 more genes
nsv4676233	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 22,868,759-34,335,753 , GRCh38.p12 chr18: 25,288,795-36,755,790	GAREM1, DHFRP1, 116 more genes
nsv3912888	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 27,024,475-37,983,616 , NCBI36 chr18: 25,278,473-36,237,614 , GRCh38 chr18: 29,444,510-40,403,652	GAREM1, KLHL14, 107 more genes
nsv4729854	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 23,971,647-33,737,300 , GRCh38.p12 chr18: 26,391,683-36,157,337	GAREM1, CLUHP6, 100 more genes
nsv3897721	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 29,711,972-35,866,193 , GRCh38.p12 chr18: 32,132,009-38,286,229	GAREM1, LOC105372073, 56 more genes
nsv6315530	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271	GAREM1, LOC105372145, 947 more genes
nsv3907444	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 12,842-78,015,180 , GRCh38.p12 chr18: 12,842-80,257,297	GAREM1, GALNT1, 947 more genes
nsv3890669	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 13,034-78,015,180 , GRCh38.p12 chr18: 13,034-80,257,297	GAREM1, MYL12B, 947 more genes
nsv3918488	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 43,345-76,068,860 , GRCh38 chr18: 53,345-80,209,986 , GRCh37 chr18: 53,345-77,967,869	GAREM1, LOC105372027, 945 more genes
nsv3924351	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 108,760-76,113,817 , GRCh38 chr18: 118,760-80,254,946 , GRCh37 chr18: 118,760-78,012,829	GAREM1, MIX23P1, 942 more genes
nsv3919004	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr18: 136,226-80,256,240 , GRCh37 chr18: 136,226-78,014,123 , NCBI36 chr18: 126,226-76,115,097	GAREM1, LIVAR, 941 more genes
nsv3899451	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 136,226-78,014,123 , GRCh38.p12 chr18: 136,226-80,256,240	GAREM1, BOLA2P1, 941 more genes
nsv3924706	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 136,227-78,014,123 , GRCh38 chr18: 136,227-80,256,240 , NCBI36 chr18: 126,227-76,115,097	GAREM1, LOC100420948, 941 more genes
nsv3907722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 136,227-78,014,123 , GRCh38.p12 chr18: 136,227-80,256,240	GAREM1, ROCK1, 941 more genes
nsv3910887	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 139,089-76,113,807 , GRCh37 chr18: 149,089-78,012,819 , GRCh38 chr18: 149,089-80,254,936	GAREM1, LPIN2, 941 more genes
nsv3912925	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr18: 138,963-76,111,023 , GRCh38 chr18: 148,963-80,252,149 , GRCh37 chr18: 148,963-78,010,032	GAREM1, LOC105372038, 941 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 42

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Number of Variants: 20

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Supplemental Content

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