dbVar for Gene (Select 8131) - 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
nsv6122555	copy number variation	1	nstd186	human		GRCh37 chr16: 181,382-181,488 , GRCh38.p12 chr16: 131,383-131,489	NPRL3
nsv6112798	copy number variation	1	nstd102	human	not provided	GRCh37 chr16: 176,680-177,522 , GRCh38.p12 chr16: 126,681-127,523	NPRL3
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
nsv5980414	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr16: 188,148-188,266 , GRCh38.p12 chr16: 138,149-138,267	NPRL3
nsv5972023	insertion	1	nstd209	human		GRCh38 chr16: 103,292-103,292 , GRCh37.p13 chr16: 153,290-153,290	NPRL3
nsv5947283	copy number variation	1	nstd209	human		GRCh38 chr16: 131,340-131,505 , GRCh37.p13 chr16: 181,339-181,504	NPRL3
nsv5880151	copy number variation	1	nstd209	human		GRCh38 chr16: 97,316-99,415 , GRCh37.p13 chr16: 147,314-149,413	NPRL3
nsv5726451	mobile element insertion	1	nstd211	human		GRCh38 chr16: 113,928-113,928 , GRCh37.p13 chr16: 163,927-163,927	NPRL3
nsv5706743	mobile element insertion	2	nstd211	human		GRCh38 chr16: 85,838-85,838 , GRCh37.p13 chr16: 135,837-135,837	MPG, NPRL3
nsv5697439	mobile element insertion	1	nstd211	human		GRCh38 chr16: 110,304-110,304 , GRCh37.p13 chr16: 160,302-160,302	NPRL3
nsv5672992	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 167,290-188,266 , GRCh38.p12 chr16: 117,291-138,267	NPRL3
nsv5672919	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 163,493-163,851 , GRCh38.p12 chr16: 113,494-113,852	NPRL3
nsv5672918	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 160,513-180,600 , GRCh38.p12 chr16: 110,515-130,601	NPRL3
nsv5672915	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 138,677-188,286 , GRCh38.p12 chr16: 88,678-138,287	NPRL3
nsv5672837	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 169,115-169,264 , GRCh38.p12 chr16: 119,116-119,265	NPRL3
nsv5672680	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 163,493-193,701 , GRCh38.p12 chr16: 113,494-143,702	NPRL3
nsv5672677	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 136,684-169,274 , GRCh38.p12 chr16: 86,685-119,275	NPRL3
nsv5672602	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 148,133-188,266 , GRCh38.p12 chr16: 98,135-138,267	NPRL3
nsv5672601	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 142,584-188,266 , GRCh38.p12 chr16: 92,586-138,267	NPRL3
nsv5603906	copy number variation	1	nstd207	human		GRCh38 chr16: 131,340-131,505 , GRCh37.p13 chr16: 181,339-181,504	NPRL3

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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

Additional filters

Links from Gene

Items: 1 to 20 of 550

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Number of Variants: 20

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Find related data

Recent activity