fign[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
nsv3876704	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 164,401,462-164,470,460 , GRCh38.p12 chr2: 163,544,952-163,613,950	FIGN
nsv3910630	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331	FIGN, DAZAP2P1, 2991 more genes
nsv4768307	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 163,078,055-182,119,617 , GRCh38.p12 chr2: 162,221,545-181,254,890	FIGN, RBM45, 258 more genes
nsv6315160	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 160,347,642-174,075,851 , GRCh38.p12 chr2: 159,491,131-173,211,123	FIGN, EIF3EP3, 158 more genes
nsv3877758	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 157,970,774-169,270,675 , GRCh38.p12 chr2: 157,114,262-168,414,165	FIGN, GCA, 121 more genes
nsv3921316	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 155,624,215-165,414,901 , GRCh37.p13 chr2: 155,915,969-165,706,655 , GRCh38.p12 chr2: 155,059,457-164,850,145	FIGN, LOC105373712, 121 more genes
nsv3904389	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 158,382,388-166,605,758 , GRCh37 chr2: 159,238,900-167,462,268 , NCBI36 chr2: 158,947,146-167,170,514	FIGN, TANC1, 95 more genes
nsv6313780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 161,551,326-167,762,790 , GRCh38.p12 chr2: 160,694,815-166,906,280	FIGN, SCN9A, 60 more genes
nsv4346986	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 162,485,583-168,295,583 , GRCh38.p12 chr2: 161,629,073-167,439,073	FIGN, CYP2C56P, 49 more genes
nsv3920656	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 164,217,738-169,989,662 , GRCh37.p13 chr2: 164,509,492-170,281,416 , GRCh38.p12 chr2: 163,652,982-169,424,906	FIGN, RNU6-766P, 48 more genes
nsv3887115	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 164,366,067-169,069,454 , GRCh38.p12 chr2: 163,509,557-168,212,944	FIGN, EIF3EP3, 32 more genes
nsv3921931	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 161,464,472-165,033,549 , GRCh37.p13 chr2: 161,756,226-165,325,303 , GRCh38.p12 chr2: 160,899,715-164,468,793	FIGN, MXRA7P1, 35 more genes
nsv3907730	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 164,020,046-167,527,078 , GRCh37 chr2: 164,311,800-167,818,832 , GRCh38 chr2: 163,455,290-166,962,322	FIGN, LOC100506124, 28 more genes
nsv3871848	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 161,542,325-164,640,864 , GRCh38.p12 chr2: 160,685,814-163,784,354	FIGN, LOC105373722, 34 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	FIGN, LOC112268439, 3737 more genes
nsv3874648	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305	FIGN, IGKV2OR2-10, 3737 more genes
nsv3885544	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609	FIGN, RNU6-674P, 3735 more genes
nsv3882615	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232	FIGN, MTND2P22, 3724 more genes
nsv4674383	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 163,233,162-211,927,188 , GRCh38.p12 chr2: 162,376,652-211,062,464	FIGN, SNORA41, 663 more genes
nsv3875392	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 152,409,978-179,325,736 , GRCh38.p12 chr2: 151,553,464-178,461,009	FIGN, MIR10B, 359 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 31

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Number of Variants: 20

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Supplemental Content

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