drg1[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
nsv6312811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 134,292,465-134,296,564 , GRCh38.p12 chr8: 133,280,222-133,284,321	NDRG1
nsv6312708	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 134,260,948-134,262,796 , GRCh38.p12 chr8: 133,248,705-133,250,553	NDRG1
nsv3887008	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 134,262,787-134,271,410 , GRCh38 chr8: 133,250,544-133,259,167	NDRG1
nsv5059944	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 134,265,064-134,265,065 , GRCh38 chr8: 133,252,821-133,252,822	NDRG1
nsv5381642	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 134,266,772-134,276,905 , GRCh38.p12 chr8: 133,254,529-133,264,662	NDRG1
nsv6312373	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 134,251,200-134,251,259 , GRCh38 chr8: 133,238,957-133,239,016	NDRG1
nsv4682848	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 134,248,414-134,310,547 , GRCh38.p12 chr8: 133,236,171-133,298,304	NDRG1
nsv5381641	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 134,251,111-134,296,564 , GRCh38.p12 chr8: 133,238,868-133,284,321	NDRG1
nsv7098161	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 134,251,121-134,296,554 , GRCh38.p12 chr8: 133,238,878-133,284,311	NDRG1
nsv6312625	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 134,274,280-134,296,564 , GRCh38.p12 chr8: 133,262,037-133,284,321	NDRG1
nsv3905095	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr6: 142,540,767-142,619,703 , GRCh38.p12 chr6: 142,219,630-142,298,566	VTA1, LINC02919
nsv3901118	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 142,410,111-142,547,236 , GRCh38.p12 chr6: 142,088,974-142,226,099	NMBR, GJE1, 1 more genes
nsv4728984	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 142,410,111-142,475,616 , GRCh38.p12 chr6: 142,088,974-142,154,479	NMBR, GJE1, 1 more genes
nsv4729105	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 142,483,642-142,786,697 , GRCh38.p12 chr6: 142,162,505-142,465,560	LINC02919, VTA1, 1 more genes
nsv7097893	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 134,107,268-134,296,554 , GRCh38.p12 chr8: 133,095,024-133,284,311	SLA, TG, 4 more genes
nsv4674996	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 126,892,814-143,750,028 , GRCh38.p12 chr8: 125,880,570-142,668,610	POU5F1B, DNAJC8P3, 158 more genes
nsv3915490	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 127,707,788-144,459,935 , GRCh37.p13 chr8: 127,638,606-144,388,560 , GRCh38.p12 chr8: 126,626,361-143,306,390	LOC107986906, MIR1208, 179 more genes
nsv4350212	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 135,239,633-146,997,510 , GRCh38.p12 chr6: 134,918,495-146,676,374	LOC100131041, ADGB-DT, 146 more genes
nsv4455511	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 124,120,772-135,265,846 , GRCh38.p12 chr8: 123,108,532-134,253,603	MTSS1, PCAT2, 148 more genes
nsv3891146	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 139,513,020-150,389,231 , GRCh38.p12 chr6: 139,191,883-150,068,095	UST, RAET1K, 131 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

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Items: 1 to 20 of 116

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Number of Variants: 20

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