traf7[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
nsv3907467	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 2,218,090-2,247,362 , GRCh38.p12 chr16: 2,168,089-2,197,361	TRAF7, CASKIN1
nsv3893007	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 1,734,363-2,285,561 , GRCh38.p12 chr16: 1,684,362-2,235,560	TRAF7, IGFALS, 49 more genes
nsv6637664	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 2,021,144-2,266,791 , GRCh38.p12 chr16: 1,971,143-2,216,790	TRAF7, SNHG19, 22 more genes
nsv6315012	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 2,066,081-2,241,220 , GRCh37.p13 chr16: 2,116,082-2,291,221	TRAF7, CASKIN1, 16 more genes
nsv6315010	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 2,047,157-2,220,112 , GRCh37.p13 chr16: 2,097,158-2,270,113	TRAF7, RAB26, 14 more genes
nsv4716573	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 2,157,801-2,288,100 , GRCh38.p12 chr16: 2,107,800-2,238,099	TRAF7, MIR3180-5, 12 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	TRAF7, 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	TRAF7, 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	TRAF7, 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	TRAF7, 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	TRAF7, FTLP14, 1868 more genes
nsv1398297	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 102,839-28,327,676 , GRCh38.p12 chr16: 52,839-28,316,355	TRAF7, BMERB1, 701 more genes
nsv3903116	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 85,880-22,442,007 , GRCh38.p12 chr16: 35,880-22,430,686	TRAF7, NPIPA8, 616 more genes
nsv3900978	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 85,880-19,806,921 , GRCh38.p12 chr16: 35,880-19,795,599	TRAF7, LOC105371091, 543 more genes
nsv3915829	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 656,663-15,744,462 , GRCh38 chr16: 666,662-15,743,104 , GRCh37 chr16: 716,662-15,836,961	TRAF7, RPL35AP34, 429 more genes
nsv3923267	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 93,732-13,420,663 , GRCh38 chr16: 43,732-13,326,806 , NCBI36 chr16: 33,732-13,328,164	TRAF7, METRN, 413 more genes
nsv3917929	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 96,766-11,619,372 , GRCh38 chr16: 46,766-11,525,516 , NCBI36 chr16: 36,766-11,526,873	TRAF7, LOC100130283, 386 more genes
nsv3913858	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 73,141-11,390,552 , GRCh38 chr16: 23,141-11,296,695 , NCBI36 chr16: 13,141-11,298,053	TRAF7, TPSP1, 382 more genes
nsv3904496	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 85,880-11,209,288 , GRCh38.p12 chr16: 35,880-11,115,431	TRAF7, HBA2, 372 more genes
nsv3896813	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 85,880-9,883,129 , GRCh38.p12 chr16: 35,880-9,789,272	TRAF7, HMOX2, 348 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 66

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Number of Variants: 20

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