lypd1[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
nsv3919382	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr2: 132,957,957-133,148,517 , GRCh37.p13 chr2: 133,241,487-133,432,047 , GRCh38.p12 chr2: 132,483,914-132,674,474	LYPD1, NCKAP5, 3 more genes
nsv3889741	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 133,295,354-133,535,250 , GRCh38.p12 chr2: 132,537,781-132,777,677	LYPD1, NCKAP5, 1 more genes
nsv3910630	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331	LYPD1, DAZAP2P1, 2991 more genes
nsv6290867	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 122,699,106-143,799,629 , GRCh38.p12 chr2: 121,941,530-143,042,060	LYPD1, RNU6-675P, 300 more genes
nsv3876229	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 120,571,363-141,627,287 , GRCh38.p12 chr2: 119,813,787-140,869,718	LYPD1, MIR9986, 320 more genes
nsv3897428	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 123,445,762-140,592,538 , NCBI36 chr2: 123,919,808-141,066,577 , GRCh37 chr2: 124,203,338-141,350,107	LYPD1, ARHGAP42P2, 278 more genes
nsv3894414	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 118,843,900-135,722,308 , GRCh38 chr2: 118,086,324-134,964,738 , NCBI36 chr2: 118,560,370-135,438,778	LYPD1, RHOQP2, 287 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	LYPD1, LOC112268439, 3737 more genes
nsv3874648	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305	LYPD1, IGKV2OR2-10, 3737 more genes
nsv3885544	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609	LYPD1, RNU6-674P, 3735 more genes
nsv3882615	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232	LYPD1, MTND2P22, 3724 more genes
nsv6291353	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 111,484,468-146,333,604 , GRCh38.p12 chr2: 110,726,891-145,576,036	LYPD1, LINC01120, 490 more genes
nsv6314748	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 112,475,655-145,691,999 , GRCh38.p12 chr2: 111,718,078-144,934,432	LYPD1, MED15P9, 474 more genes
nsv6314726	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196	LYPD1, ACTG2, 1713 more genes
nsv4684238	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr2: 122,952,356-133,826,358 , GRCh38.p12 chr2: 122,194,780-133,068,785	LYPD1, BIN1, 211 more genes
nsv6637034	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 133,281,344-134,072,006 , GRCh38.p12 chr2: 132,523,771-133,314,434	LYPD1, NCKAP5, 5 more genes
nsv3923963	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr2: 110,190,938-242,751,149 , GRCh37.p13 chr2: 110,833,649-243,102,476 , GRCh38.p12 chr2: 110,076,072-242,160,331	LYPD1, NMTRQ-TTG9-1, 1944 more genes
nsv3876086	copy number variation	1	nstd102	human	drug response	GRCh37 chr2: 104,172,062-168,223,828 , GRCh38.p12 chr2: 103,555,604-167,367,318	LYPD1, SLC4A10, 871 more genes
nsv3924199	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr2: 130,861,065-242,751,149 , GRCh37.p13 chr2: 131,144,595-243,102,476 , GRCh38.p12 chr2: 130,387,022-242,160,331	LYPD1, METAP1D, 1635 more genes
nsv3873155	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 130,920,847-134,220,436 , GRCh38.p12 chr2: 130,163,274-133,462,865	LYPD1, LOC440910, 119 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

Additional filters

Search results

Items: 1 to 20 of 21

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Number of Variants: 20

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Supplemental Content

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Search details

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