dbVar for Gene (Select 6621) - 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
nsv5955311	insertion	1	nstd209	human		GRCh38 chr9: 136,387,903-136,387,903 , GRCh37.p13 chr9: 139,282,355-139,282,355	SNAPC4
nsv5911764	copy number variation	1	nstd209	human		GRCh38 chr9: 136,378,012-136,378,062 , GRCh37.p13 chr9: 139,272,464-139,272,514	SNAPC4
nsv5537860	insertion	1	nstd206	human		GRCh38 chr9: 136,387,921-136,387,955 , GRCh37.p13 chr9: 139,282,373-139,282,407	SNAPC4
nsv5477981	copy number variation	1	nstd206	human		GRCh38 chr9: 136,389,538-136,389,599 , GRCh37.p13 chr9: 139,283,990-139,284,051	SNAPC4
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
nsv5246206	copy number variation	1	nstd204	human		GRCh38.p13 chr9: 136,043,001-136,766,200 , GRCh37.p13 chr9: 138,934,847-139,660,652	MIR4674, TMEM250, 37 more genes
nsv4985863	copy number variation	1	nstd200	human		GRCh38 chr9: 136,239,913-136,449,610 , GRCh37.p13 chr9: 139,131,759-139,344,062	CCDC187, SNAPC4, 9 more genes
nsv4973353	copy number variation	1	nstd200	human		GRCh38 chr9: 136,396,296-136,409,434 , GRCh37.p13 chr9: 139,290,748-139,303,886	PMPCA, SNAPC4, 1 more genes
nsv4848135	copy number variation	1	nstd200	human		GRCh37 chr9: 139,290,748-139,303,886 , GRCh38.p12 chr9: 136,396,296-136,409,434	PMPCA, SNAPC4, 1 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
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
nsv4602147	copy number variation	1	nstd183	human		GRCh37 chr9: 139,285,655-139,469,054 , GRCh38.p12 chr9: 136,391,203-136,574,602	NOTCH1, C9orf163, 8 more genes
nsv4578341	copy number variation	1	nstd182	human		GRCh37 chr9: 139,252,010-139,435,356 , GRCh38.p12 chr9: 136,357,558-136,540,904	NOTCH1, SNAPC4, 9 more genes
nsv4555230	insertion	1	nstd166	human		GRCh37.p13 chr9: 139,282,356-139,282,356 , GRCh38.p12 chr9: 136,387,904-136,387,904	SNAPC4
nsv4525777	copy number variation	1	nstd166	human		GRCh37.p13 chr9: 139,279,598-139,303,655 , GRCh38.p12 chr9: 136,385,146-136,409,203	ENTR1, PMPCA, 1 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
nsv4455089	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr9: 139,268,640-139,329,037 , GRCh38.p12 chr9: 136,374,188-136,434,585	SNAPC4, PMPCA, 2 more genes

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Number of Variants: 20

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Organism

Variant Type

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Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 389

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Number of Variants: 20

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