dbVar for Gene (Select 100422860) - 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
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	ARRDC1, SETP5, 101 more genes
nsv5243680	copy number variation	1	nstd204	human		GRCh38.p13 chr9: 136,802,801-136,886,500 , GRCh37.p13 chr9: 139,697,253-139,780,952	CCDC183, AJM1, 11 more genes
nsv4985870	copy number variation	1	nstd200	human		GRCh38 chr9: 136,632,294-136,850,190 , GRCh37.p13 chr9: 139,526,746-139,744,642	CCDC183, PHPT1, 25 more genes
nsv4985869	copy number variation	1	nstd200	human		GRCh38 chr9: 136,591,087-136,947,348 , GRCh37.p13 chr9: 139,485,539-139,841,800	LOC102724193, AJM1, 34 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
nsv4729067	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 139,420,166-139,787,562 , GRCh38.p12 chr9: 136,525,714-136,893,110	LCN6, LCN15, 34 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
nsv4683252	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr9: 138,594,085-140,062,314 , GRCh38.p12 chr9: 135,702,239-137,167,862	SAPCD2, MIR3621, 81 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
nsv4457273	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936	CDRT15P14, MIR548AW, 2167 more genes
nsv4455186	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937	LOC105376327, ENG, 1304 more genes
nsv4386956	copy number variation	1	nstd173	human		GRCh37 chr9: 139,721,219-139,753,306 , GRCh38.p12 chr9: 136,826,767-136,858,854	AJM1, MIR4292, 3 more genes
nsv4383485	copy number variation	1	nstd173	human		GRCh37 chr9: 139,059,275-140,803,861 , GRCh38.p12 chr9: 136,167,429-137,909,409	, LRRC26, 107 more genes
nsv4367274	copy number variation	1	nstd173	human		GRCh37 chr9: 139,563,040-140,180,735 , GRCh38.p12 chr9: 136,668,588-137,286,283	, LCN10, 67 more genes
nsv4340169	sequence alteration	1	nstd166	human		GRCh37.p13 chr9: 138,768,590-139,729,186 , GRCh38.p12 chr9: 135,876,744-136,834,734	, UBAC1, 49 more genes
nsv3971156	insertion	1	nstd168	human		GRCh38 chr9: 136,796,425-136,830,173 , GRCh37.p13 chr9: 139,690,877-139,724,625	RABL6, CCDC183, 4 more genes
nsv3924922	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 133,504,071-138,159,073 , NCBI36 chr9: 135,314,179-140,173,346 , GRCh37 chr9: 136,324,358-141,053,525	SETP5, NRARP, 178 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	NRARP, MAN1B1-DT, 104 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
nsv3922684	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897	TDRD7, CDK9, 2170 more genes

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Number of Variants: 20

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Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Study Type

Subject Phenotype Status

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Items: 1 to 20 of 353

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Number of Variants: 20

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