apc2[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
nsv7095190	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 1,455,264-1,455,852 , GRCh38.p12 chr19: 1,455,265-1,455,853	APC2
nsv3899657	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 1,460,835-1,472,007 , GRCh38.p12 chr19: 1,460,836-1,472,008	APC2, C19orf25
nsv3909219	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 1,457,002-1,488,257 , GRCh38.p12 chr19: 1,457,003-1,488,258	APC2, PCSK4, 1 more genes
nsv3904499	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 1,460,473-1,488,257 , GRCh38.p12 chr19: 1,460,474-1,488,258	APC2, PCSK4, 1 more genes
nsv3893481	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 1,460,795-1,488,242 , GRCh38.p12 chr19: 1,460,796-1,488,243	APC2, PCSK4, 1 more genes
nsv1398495	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 1,453,071-1,481,983 , GRCh38 chr19: 1,453,072-1,481,984	APC2, PCSK4, 1 more genes
nsv7095269	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 1,465,134-1,497,210 , GRCh38.p12 chr19: 1,465,135-1,497,211	APC2, C19orf25, 2 more genes
nsv3918779	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 137,320,520-141,049,374 , NCBI36 chr9: 136,460,341-140,169,195 , GRCh38 chr9: 134,428,674-138,154,922	LRRC26, SOCS5P2, 160 more genes
nsv3891854	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 137,816,459-141,114,095 , GRCh38.p12 chr9: 134,924,613-138,223,645	LCN10, LINC01502, 147 more genes
nsv3899903	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 138,209,358-141,020,389 , GRCh38.p12 chr9: 135,317,512-138,125,937	NSMF, OBP2A, 137 more genes
nsv3896336	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 138,222,049-141,018,925 , GRCh38.p12 chr9: 135,330,203-138,124,473	LINC02907, PAEPP1, 137 more genes
nsv4685995	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 138,225,001-141,015,001 , GRCh38.p12 chr9: 135,333,155-138,120,549	TPRN, CCDC183, 137 more genes
nsv7098070	copy number variation	3	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr9: 138,392,557-141,016,451 , GRCh38.p12 chr9: 135,500,711-138,121,999	STPG3-AS1, CACNA1B-AS1, 132 more genes
nsv7093414	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 134,932,722-137,269,957 , GRCh37.p13 chr9: 137,824,568-140,164,409	LHX3, FUT7, 121 more genes
nsv6313935	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 138,740,078-141,020,389 , GRCh38.p12 chr9: 135,848,232-138,125,937	ENTR1, LINC02692, 115 more genes
nsv3922926	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 137,483,683-139,628,011 , GRCh37 chr9: 138,343,862-140,508,190 , GRCh38 chr9: 135,452,016-137,613,738	SSNA1, LOC107987140, 126 more genes
nsv4681206	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr9: 138,645,763-140,729,425 , GRCh38.p12 chr9: 135,753,917-137,834,973	DPP7, MIR4673, 112 more genes
nsv4768352	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 139,018,777-141,018,984 , GRCh38.p12 chr9: 136,126,931-138,124,532	MIR6722, EXD3, 108 more genes
nsv7098071	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr9: 139,089,171-141,016,451 , GRCh38.p12 chr9: 136,197,325-138,121,999	NPDC1, LOC101928786, 108 more genes
nsv3915405	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 136,323,974-138,124,532 , NCBI36 chr9: 138,338,249-140,138,805 , GRCh37 chr9: 139,218,428-141,018,984	MIR6722, TOR4A, 105 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 132

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Number of Variants: 20

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