dbVar for Gene (Select 11211) - 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
nsv5494141	copy number variation	1	nstd206	human		GRCh38 chr12: 129,527,330-130,603,455 , GRCh37.p13 chr12: 130,011,875-131,088,000	LINC02419, RIMBP2, 10 more genes
nsv5276501	copy number variation	1	nstd204	human		GRCh38.p13 chr12: 130,054,901-130,248,200 , GRCh37.p13 chr12: 130,539,446-130,732,745	LOC105370077, LINC02419, 3 more genes
nsv4729329	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr12: 130,192,184-131,023,667 , GRCh38.p12 chr12: 129,707,639-130,539,122	RPS20P30, FZD10, 10 more genes
nsv4456888	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 126,470,636-133,777,902 , GRCh38.p12 chr12: 125,986,090-133,201,316	LINC02347, LOC107987176, 145 more genes
nsv4416499	copy number variation	1	nstd174	human		GRCh37 chr12: 130,423,119-130,718,971 , GRCh38.p12 chr12: 129,938,574-130,234,426	FZD10, FZD10-AS1, 5 more genes
nsv4349911	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 125,451,405-133,810,935 , GRCh38.p12 chr12: 124,966,859-133,234,349	LOC107987177, GOLGA3, 159 more genes
nsv3924220	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr12: 115,131,583-133,166,920 , NCBI36 chr12: 114,053,771-132,253,579 , GRCh37 chr12: 115,569,388-133,743,506	LOC105370080, LINC02985, 376 more genes
nsv3923347	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 119,619,858-132,289,149 , GRCh37 chr12: 121,135,475-133,779,076 , GRCh38 chr12: 120,697,672-133,202,490	LOC105370044, RNU6-1017P, 273 more genes
nsv3921145	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 123,929,305-133,767,986 , GRCh38 chr12: 123,444,758-133,191,400 , NCBI36 chr12: 122,495,258-132,278,059	ZNF268, PTP4A1P2, 193 more genes
nsv3920557	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 118,603,264-133,758,908 , GRCh38 chr12: 118,165,459-133,182,322 , NCBI36 chr12: 117,087,647-132,268,981	TMED2, GCN1, 339 more genes
nsv3915906	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr12: 126,403,612-133,166,920 , GRCh37 chr12: 126,888,158-133,743,506 , NCBI36 chr12: 125,454,111-132,253,579	FBRSL1, P2RX2, 135 more genes
nsv3914999	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 122,035,702-129,765,072 , GRCh38 chr12: 122,985,202-130,714,574 , GRCh37 chr12: 123,469,749-131,199,119	LINC00944, ATP6V0A2, 132 more genes
nsv3914194	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807	, BTG1P1, 2451 more genes
nsv3913894	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 113,190,591-132,287,975 , GRCh38 chr12: 114,268,403-133,201,316 , GRCh37 chr12: 114,706,208-133,777,902	TAOK3, LINC02405, 386 more genes
nsv3911281	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr12: 123,509,825-133,191,400 , GRCh37 chr12: 123,994,372-133,767,986 , NCBI36 chr12: 122,560,325-132,278,059	TMEM132C, RPL23AP67, 192 more genes
nsv3905447	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316	, LOH12CR2, 2452 more genes
nsv3904719	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 621,220-133,779,118 , GRCh38.p12 chr12: 512,054-133,202,532	, OR5BT1P, 2441 more genes
nsv3904242	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309	, RNA5SP369, 2454 more genes
nsv3897722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 191,619-133,777,645 , GRCh38.p12 chr12: 82,453-133,201,059	, RNU4ATAC16P, 2452 more genes
nsv3896575	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 120,367,241-133,777,645 , GRCh38.p12 chr12: 119,929,437-133,201,059	LOC107984448, LOC105370082, 306 more genes

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Number of Variants: 20

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Organism

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 97

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Number of Variants: 20

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