tnfrsf4[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
nsv3888775	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 1,130,727-1,154,157 , GRCh38.p12 chr1: 1,195,347-1,218,777	TNFRSF4, TNFRSF18, 2 more genes
nsv5381061	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr1: 1,146,915-1,168,668 , GRCh38.p12 chr1: 1,211,535-1,233,288	TNFRSF4, B3GALT6, 1 more genes
nsv7095697	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 1,146,935-1,168,648 , GRCh38.p12 chr1: 1,211,555-1,233,268	TNFRSF4, SDF4, 1 more genes
nsv6290672	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 849,466-17,525,065 , GRCh38.p12 chr1: 914,086-17,198,570	TNFRSF4, RPL9P11, 466 more genes
nsv3873030	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 746,608-15,077,159 , GRCh38.p12 chr1: 811,228-14,750,663	TNFRSF4, RN7SL451P, 376 more genes
nsv3888433	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-12,699,337 , GRCh38.p12 chr1: 82,154-12,639,316	TNFRSF4, AURKAIP1, 356 more genes
nsv4436105	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-11,784,118 , GRCh38.p12 chr1: 82,154-11,724,061	TNFRSF4, PARK7, 325 more genes
nsv3899046	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 844,347-12,470,133 , GRCh37 chr1: 779,727-12,530,188 , NCBI36 chr1: 769,590-12,452,775	TNFRSF4, PRKCZ-DT, 315 more genes
nsv6637093	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 849,467-12,448,956 , GRCh38.p12 chr1: 914,087-12,388,897	TNFRSF4, VWA1, 311 more genes
nsv6315409	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 849,466-10,258,804 , GRCh38.p12 chr1: 914,086-10,198,746	TNFRSF4, VAMP3, 245 more genes
nsv4436631	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 554,375-9,779,842 , GRCh38.p12 chr1: 618,995-9,719,784	TNFRSF4, LINC02606, 253 more genes
nsv3913374	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 4,737-8,767,973 , GRCh37.p13 chr1: 14,874-8,845,386 , GRCh38.p12 chr1: 14,874-8,785,327	TNFRSF4, LOC105378593, 252 more genes
nsv3907841	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 837,491-9,616,363 , GRCh38 chr1: 902,111-9,556,305 , NCBI36 chr1: 827,354-9,538,950	TNFRSF4, PRKCZ-AS1, 224 more genes
nsv3890178	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 839,329-9,549,767 , GRCh37 chr1: 849,466-9,627,180 , GRCh38 chr1: 914,086-9,567,122	TNFRSF4, ANKRD65, 224 more genes
nsv3909850	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 846,680-9,389,984 , GRCh38 chr1: 911,300-9,329,925 , NCBI36 chr1: 836,543-9,312,571	TNFRSF4, LOC105378590, 221 more genes
nsv3889222	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 849,466-8,901,938 , GRCh38.p12 chr1: 914,086-8,841,879	TNFRSF4, PLEKHG5, 205 more genes
nsv3894118	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 554,268-8,520,391 , GRCh38 chr1: 629,025-8,537,745 , GRCh37 chr1: 564,405-8,597,804	TNFRSF4, TNFRSF14, 223 more genes
nsv3898457	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 859,215-8,747,647 , GRCh37 chr1: 794,595-8,807,706 , NCBI36 chr1: 784,458-8,730,293	TNFRSF4, NOC2L, 205 more genes
nsv3885153	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-7,936,272 , GRCh38.p12 chr1: 82,154-7,876,212	TNFRSF4, TTLL10-AS1, 226 more genes
nsv4435992	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-7,637,060 , GRCh38.p12 chr1: 82,154-7,577,000	TNFRSF4, SNORD167, 222 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 170

Page of 9

Number of Variants: 20

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Supplemental Content

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Search details

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