sec14l5[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
nsv4675986	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 5,023,441-5,080,086 , GRCh38.p12 chr16: 4,973,440-5,030,085	SEC14L5, NAGPA
nsv6291523	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr16: 4,971,767-5,023,403 , GRCh38.p12 chr16: 4,921,766-4,973,402	SEC14L5, PPL, 1 more genes
nsv3912877	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 2,900,735-7,160,698 , NCBI36 chr16: 2,840,736-7,100,699 , GRCh38 chr16: 2,850,734-7,110,697	SEC14L5, TRP-CGG1-2, 129 more genes
nsv3909798	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 3,146,027-6,362,229 , GRCh38.p12 chr16: 3,096,026-6,312,228	SEC14L5, LINC01569, 102 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	SEC14L5, 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	SEC14L5, 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	SEC14L5, 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	SEC14L5, 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	SEC14L5, 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	SEC14L5, BMERB1, 701 more genes
nsv4729901	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 2,959,279-30,190,593 , GRCh38.p12 chr16: 2,909,278-30,179,272	SEC14L5, NPIPB9, 597 more genes
nsv6637429	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029	SEC14L5, MIR6511B2, 535 more genes
nsv3910441	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 4,634,894-29,089,642 , GRCh37 chr16: 4,694,893-29,182,141 , GRCh38 chr16: 4,644,892-29,170,820	SEC14L5, LOC729945, 450 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	SEC14L5, 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	SEC14L5, 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	SEC14L5, 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	SEC14L5, 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	SEC14L5, 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	SEC14L5, 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	SEC14L5, HBA2, 372 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 34

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Number of Variants: 20

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Supplemental Content

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