ajm1[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
nsv3904253	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 139,739,420-139,744,458 , GRCh38.p12 chr9: 136,844,968-136,850,006	AJM1, PHPT1
nsv3907951	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 139,726,282-139,756,883 , GRCh38.p12 chr9: 136,831,830-136,862,431	AJM1, MAMDC4, 3 more genes
nsv3908063	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 139,726,282-139,754,431 , GRCh38.p12 chr9: 136,831,830-136,859,979	AJM1, RABL6, 2 more genes
nsv3894197	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 139,726,282-139,754,427 , GRCh38.p12 chr9: 136,831,830-136,859,975	AJM1, MAMDC4, 2 more genes
nsv3908385	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 139,728,202-139,754,427 , GRCh38.p12 chr9: 136,833,750-136,859,975	AJM1, PHPT1, 2 more genes
nsv3893346	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 139,726,282-139,751,625 , GRCh38.p12 chr9: 136,831,830-136,857,173	AJM1, MAMDC4, 2 more genes
nsv3906464	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 139,728,202-139,751,625 , GRCh38.p12 chr9: 136,833,750-136,857,173	AJM1, PHPT1, 2 more genes
nsv3898820	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 139,728,202-139,751,183 , GRCh38.p12 chr9: 136,833,750-136,856,731	AJM1, RABL6, 2 more genes
nsv3903184	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 139,726,282-139,749,102 , GRCh38.p12 chr9: 136,831,830-136,854,650	AJM1, RABL6, 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	AJM1, 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	AJM1, 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	AJM1, 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	AJM1, 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	AJM1, 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	AJM1, 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	AJM1, 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	AJM1, 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	AJM1, 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	AJM1, DPP7, 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	AJM1, MIR6722, 108 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 77

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Number of Variants: 20

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