foxp4[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 12

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3885596	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 41,504,126-41,514,706 , GRCh38.p12 chr6: 41,536,388-41,546,968	FOXP4, FOXP4-AS1
nsv3872719	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 41,514,247-41,514,706 , GRCh38.p12 chr6: 41,546,509-41,546,968	FOXP4, FOXP4-AS1
nsv3876335	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 41,514,298-41,514,706 , GRCh38.p12 chr6: 41,546,560-41,546,968	FOXP4, FOXP4-AS1
nsv3919521	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 37,853,123-45,729,558 , GRCh37 chr6: 37,745,145-45,621,580 , GRCh38 chr6: 37,777,369-45,653,843	FOXP4, RPL23P6, 184 more genes
nsv7097826	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 41,126,341-43,752,536 , GRCh38.p12 chr6: 41,158,603-43,784,799	FOXP4, USP49, 96 more genes
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	FOXP4, LOC105378061, 2914 more genes
nsv3879811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083	FOXP4, RNU6-411P, 2910 more genes
nsv3887898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394	FOXP4, SOD1P1, 2905 more genes
nsv3889814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382	FOXP4, ITPR3, 2905 more genes
nsv4350067	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650	FOXP4, HLA-DPB2, 1001 more genes
nsv3913920	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028	FOXP4, TRR-ACG1-2, 1385 more genes
nsv7097825	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 41,126,341-43,737,486 , GRCh38.p12 chr6: 41,158,603-43,769,749	FOXP4, DNPH1, 96 more genes

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foxp4[All Fields] AND 1[has_clinical] (13)
dbVar
Mus musculus RAB3C, member RAS oncogene family (Rab3c), transcript variant 2, mR...
Mus musculus RAB3C, member RAS oncogene family (Rab3c), transcript variant 2, mRNA
gi|1335348646|ref|NM_001360099.1|

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