dbVar for Gene (Select 100188847) - 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
nsv6112799	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 2,089,795-2,185,919 , GRCh38.p12 chr16: 2,039,794-2,135,918	NTHL1, PKD1, 6 more genes
nsv6112797	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012	ANTKMT, HBA1, 307 more genes
nsv6112776	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 2,140,783-2,187,415 , GRCh38.p12 chr16: 2,090,782-2,137,414	PKD1, MIR1225, 4 more genes
nsv5980385	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 2,098,616-2,138,611 , GRCh38.p12 chr16: 2,048,615-2,088,610	MIR1225, PKD1, 1 more genes
nsv5939446	copy number variation	1	nstd209	human		GRCh38 chr16: 2,089,303-2,089,359 , GRCh37.p13 chr16: 2,139,304-2,139,360	PKD1, TSC2, 1 more genes
nsv5672994	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr16: 2,133,686-2,138,611 , GRCh38.p12 chr16: 2,083,685-2,088,610	PKD1, TSC2, 1 more genes
nsv5672839	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 2,103,323-2,185,710 , GRCh38.p12 chr16: 2,053,322-2,135,709	PKD1, TSC2, 5 more genes
nsv5380998	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr16: 624,055-2,153,916 , GRCh38.p12 chr16: 574,055-2,103,915	NDUFB10, BAIAP3, 102 more genes
nsv5380995	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 2,098,597-2,550,979 , GRCh38.p12 chr16: 2,048,596-2,500,978	TEDC2, MIR3677HG, 33 more genes
nsv5380854	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 2,114,263-2,141,185 , GRCh38.p12 chr16: 2,064,262-2,091,184	TSC2, PKD1-AS1, 2 more genes
nsv5271137	copy number variation	1	nstd204	human		GRCh38.p13 chr16: 1,615,401-2,135,300 , GRCh37.p13 chr16: 1,665,402-2,185,301	SNHG9, SNORA64, 40 more genes
nsv5269318	copy number variation	1	nstd204	human		GRCh38.p13 chr16: 1,733,301-3,469,700 , GRCh37.p13 chr16: 1,783,302-3,519,700	, MIR6511B1, 156 more genes
nsv5266471	copy number variation	1	nstd204	human		GRCh38.p13 chr16: 1,936,501-2,552,200 , GRCh37.p13 chr16: 1,986,502-2,602,201	AMDHD2, MIR3178, 56 more genes
nsv5265522	copy number variation	1	nstd204	human		GRCh38.p13 chr16: 53,201-2,576,200 , GRCh37.p13 chr16: 103,201-2,626,201	, RHBDL1, 175 more genes
nsv5007907	copy number variation	1	nstd200	human		GRCh38 chr16: 2,088,374-2,088,460 , GRCh37.p13 chr16: 2,138,375-2,138,461	PKD1, MIR1225, 1 more genes
nsv4729241	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 85,880-5,249,457 , GRCh38.p12 chr16: 35,880-5,199,456	MTRNR2L4, BRICD5, 307 more genes
nsv4728874	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 2,011,148-2,161,281 , GRCh38.p12 chr16: 1,961,147-2,111,280	NTHL1, SNORA78, 19 more genes
nsv4683469	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 2,108,738-2,143,097 , GRCh38.p12 chr16: 2,058,737-2,093,096	PKD1-AS1, TSC2, 2 more genes
nsv4683390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 624,055-2,148,005 , GRCh38.p12 chr16: 574,055-2,098,004	MRPS34, HAGHL, 102 more genes
nsv4683209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 1,203,718-2,185,710 , GRCh38.p12 chr16: 1,153,718-2,135,709	TMEM204, UQCC4, 67 more genes

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Number of Variants: 20

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Result Filters

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Organism

Variant Type

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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 390

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Number of Variants: 20

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