dpp7[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
nsv3892169	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 140,003,586-140,007,653 , GRCh38.p12 chr9: 137,109,134-137,113,201	DPP7, MAN1B1
nsv7097704	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 140,000,557-140,003,043 , GRCh38.p12 chr9: 137,106,105-137,108,591	DPP7, MAN1B1
nsv6313265	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 139,981,452-140,040,374 , GRCh38.p12 chr9: 137,087,000-137,145,922	DPP7, MAN1B1, 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	DPP7, LRRC26, 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	DPP7, LCN10, 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	DPP7, NSMF, 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	DPP7, LINC02907, 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	DPP7, TPRN, 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	DPP7, STPG3-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	DPP7, LHX3, 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	DPP7, ENTR1, 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	DPP7, SSNA1, 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	DPP7, MIR6722, 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	DPP7, NPDC1, 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	DPP7, MIR6722, 105 more genes
nsv3908837	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 139,282,807-141,020,389 , GRCh38.p12 chr9: 136,388,355-138,125,937	DPP7, SNORA17B, 101 more genes
nsv5381762	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 139,284,464-141,018,984 , GRCh38.p12 chr9: 136,390,012-138,124,532	DPP7, ARRDC1, 101 more genes
nsv3924554	copy number variation	2	nstd102	human	Pathogenic	GRCh38 chr9: 136,323,974-138,014,606 , NCBI36 chr9: 138,338,249-140,028,879 , GRCh37 chr9: 139,218,428-140,909,058	DPP7, NRARP, 104 more genes
nsv5381736	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 139,764,148-141,066,491 , GRCh38.p12 chr9: 136,869,696-138,172,039	DPP7, PTGDS, 63 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 72

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Number of Variants: 20

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