tradd[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
nsv3916762	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 62,213,235-67,804,317 , GRCh38 chr16: 62,179,331-67,770,414 , NCBI36 chr16: 60,770,736-66,361,818	TRADD, RANBP10, 87 more genes
nsv4675201	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 65,669,673-70,180,183 , GRCh38.p12 chr16: 65,635,770-70,146,280	TRADD, LOC100420066, 143 more genes
nsv3910745	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 62,902,680-66,653,415 , GRCh38 chr16: 64,311,275-68,062,011 , GRCh37 chr16: 64,345,179-68,095,914	TRADD, PSMB10, 95 more genes
nsv7094682	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr16: 65,821,800-67,208,957 , GRCh38.p12 chr16: 65,787,897-67,175,054	TRADD, RNA5SP428, 38 more genes
nsv3918405	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 66,245,888-67,473,023 , NCBI36 chr16: 64,837,292-66,064,427 , GRCh37 chr16: 66,279,791-67,506,926	TRADD, PLEKHG4, 53 more genes
nsv3923505	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 65,285,584-66,456,849 , GRCh37 chr16: 66,728,083-67,899,348 , GRCh38 chr16: 66,694,180-67,865,445	TRADD, DYNC1LI2, 56 more genes
nsv4350223	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 67,132,790-68,166,320 , GRCh38.p12 chr16: 67,098,887-68,132,417	TRADD, CBFB, 55 more genes
nsv3906108	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224	TRADD, CKLF, 1882 more genes
nsv3904593	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973	TRADD, LOC100128079, 1879 more genes
nsv3901410	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287	TRADD, LINC02175, 1877 more genes
nsv3909417	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867	TRADD, PRSS53, 1868 more genes
nsv3892266	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654	TRADD, FTLP14, 1868 more genes
nsv3921269	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345	TRADD, LOC105371237, 985 more genes
nsv6314755	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654	TRADD, ATMIN, 826 more genes
nsv3915506	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 51,490,596-88,682,563 , GRCh38 chr16: 52,899,183-90,088,654 , GRCh37 chr16: 52,933,095-90,155,062	TRADD, CFAP69P1, 716 more genes
nsv3891306	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 57,051,473-89,797,669 , GRCh38.p12 chr16: 57,017,561-89,731,261	TRADD, LOC107984894, 613 more genes
nsv3913913	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 62,980,782-88,675,894 , GRCh38 chr16: 64,389,378-90,081,985 , GRCh37 chr16: 64,423,281-90,148,393	TRADD, ATP5F1AP3, 534 more genes
nsv3919817	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 63,904,799-88,675,894 , GRCh37 chr16: 65,347,298-90,148,393 , GRCh38 chr16: 65,313,395-90,081,985	TRADD, LOC105376772, 527 more genes
nsv3910304	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 64,102,887-88,690,904 , GRCh38 chr16: 65,511,483-90,096,995 , GRCh37 chr16: 65,545,386-90,163,403	TRADD, MC1R, 528 more genes
nsv3920399	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 61,517,334-83,176,902 , GRCh37 chr16: 62,959,833-84,619,401 , GRCh38 chr16: 62,925,929-84,585,795	TRADD, LOC654780, 385 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 48

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Number of Variants: 20

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Supplemental Content

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Search details

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