ahsg[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
nsv3915488	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 185,203,637-197,837,049 , NCBI36 chr3: 186,686,331-199,321,446 , GRCh38 chr3: 185,485,849-198,110,178	AHSG, SNAR-I, 260 more genes
nsv3914166	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 180,856,452-192,229,812 , GRCh38 chr3: 181,138,664-192,512,023 , NCBI36 chr3: 182,339,146-193,712,506	AHSG, SNORA4, 199 more genes
nsv3920607	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 187,082,628-197,946,692 , GRCh37.p13 chr3: 185,599,934-196,462,295 , GRCh38.p12 chr3: 185,882,146-196,735,424	AHSG, FGF12, 212 more genes
nsv3882335	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 182,650,681-191,275,809 , GRCh38.p12 chr3: 182,932,893-191,558,020	AHSG, VPS8, 171 more genes
nsv6313539	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 182,189,525-187,212,935 , GRCh38.p12 chr3: 182,471,737-187,495,147	AHSG, ALG3, 133 more genes
nsv3884529	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 186,291,045-191,037,240 , GRCh38.p12 chr3: 186,573,256-191,319,451	AHSG, TPRG1-AS2, 75 more genes
nsv6315366	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 183,556,940-188,083,060 , GRCh38.p12 chr3: 183,839,152-188,365,272	AHSG, MASP1, 115 more genes
nsv3875526	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 184,300,169-188,285,627 , GRCh38.p12 chr3: 184,582,381-188,567,839	AHSG, RPL29P9, 78 more genes
nsv4728604	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 182,877,291-186,830,759 , GRCh38.p12 chr3: 183,159,503-187,112,971	AHSG, LOC105374253, 111 more genes
nsv3886610	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 183,178,932-186,838,042 , GRCh38.p12 chr3: 183,461,144-187,120,254	AHSG, HTR3D, 104 more genes
nsv3876960	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 186,018,854-189,514,047 , GRCh38.p12 chr3: 186,301,065-189,796,258	AHSG, ADIPOQ, 60 more genes
nsv4674249	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 185,879,162-187,446,035 , GRCh38.p12 chr3: 186,161,373-187,728,247	AHSG, RTP1, 43 more genes
nsv3884018	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 185,419,048-186,575,415 , GRCh38.p12 chr3: 185,701,260-186,857,626	AHSG, SNORA63B, 33 more genes
nsv4683580	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 186,256,465-187,009,440 , GRCh38.p12 chr3: 186,538,676-187,291,652	AHSG, RPL39P19, 32 more genes
nsv3880942	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 186,256,465-186,980,528 , GRCh38.p12 chr3: 186,538,676-187,262,740	AHSG, SNORA81, 31 more genes
nsv3885606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156	AHSG, RNU4-62P, 2880 more genes
nsv3889228	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115	AHSG, NDUFB4, 2876 more genes
nsv3880617	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391	AHSG, RPL23AP49, 2875 more genes
nsv3918981	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446	AHSG, LINC02614, 1469 more genes
nsv3918692	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 147,521,892-198,096,565 , GRCh37 chr3: 147,239,679-197,823,436 , NCBI36 chr3: 148,722,369-199,307,833	AHSG, LOC105374179, 785 more genes

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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 45

Page of 3

Number of Variants: 20

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Supplemental Content

Find related data

Search details

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