dbVar for Gene (Select 100616301) - 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
nsv5564514	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 139,315,643-139,465,759 , GRCh38.p12 chr9: 136,421,191-136,571,307	NOTCH1, SEC16A, 6 more genes
nsv5564455	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 139,297,240-139,572,028 , GRCh38.p12 chr9: 136,402,788-136,677,576	LOC105376325, NOTCH1, 14 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	ARRDC1, SETP5, 101 more genes
nsv5381680	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 139,390,513-139,440,248 , GRCh38.p12 chr9: 136,496,061-136,545,796	MIR4674, NOTCH1, 1 more genes
nsv5249366	copy number variation	1	nstd204	human		GRCh38.p13 chr9: 136,536,101-136,611,200 , GRCh37.p13 chr9: 139,430,553-139,505,652	MIR4674, LINC01451, 2 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
nsv4985868	copy number variation	1	nstd200	human		GRCh38 chr9: 136,528,503-136,809,431 , GRCh37.p13 chr9: 139,422,955-139,703,883	LCN6, DIPK1B, 25 more genes
nsv4845671	copy number variation	1	nstd200	human		GRCh37 chr9: 139,422,955-139,703,883 , GRCh38.p12 chr9: 136,528,503-136,809,431	TMEM141, CCDC183, 25 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
nsv4612627	copy number variation	1	nstd183	human		GRCh37 chr9: 139,431,355-139,530,152 , GRCh38.p12 chr9: 136,536,903-136,635,700	LINC01451, NALT1, 2 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
nsv4602098	copy number variation	1	nstd183	human		GRCh37 chr9: 139,326,816-139,632,028 , GRCh38.p12 chr9: 136,432,364-136,737,576	DIPK1B, HSPC324, 17 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
nsv4453020	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 138,594,085-139,440,258 , GRCh38.p12 chr9: 135,702,239-136,545,806	C9orf163, LOC107987140, 24 more genes
nsv4451709	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr9: 138,683,633-139,440,248 , GRCh38.p12 chr9: 135,791,787-136,545,796	SNAPC4, LOC107987140, 23 more genes

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 374

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Number of Variants: 20

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