pamr1[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
nsv5380796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397	PAMR1, FAUP4, 2031 more genes
nsv3922664	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 22,550,115-38,199,159 , NCBI36 chr11: 22,528,237-38,177,285 , GRCh37 chr11: 22,571,661-38,220,709	PAMR1, CSTF3, 170 more genes
nsv3898805	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 27,588,560-41,770,792 , GRCh38.p12 chr11: 27,567,013-41,749,242	PAMR1, LINC02707, 150 more genes
nsv4455873	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 22,079,154-35,597,645 , GRCh38.p12 chr11: 22,057,608-35,576,097	PAMR1, DNAJC24, 153 more genes
nsv3907223	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 24,469,451-37,524,085 , GRCh38.p12 chr11: 24,447,905-37,502,535	PAMR1, PIGCP1, 151 more genes
nsv3906552	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 30,615,127-40,606,139 , GRCh38.p12 chr11: 30,593,580-40,584,589	PAMR1, MIR3973, 113 more genes
nsv3908389	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 25,771,208-35,614,978 , GRCh38.p12 chr11: 25,749,661-35,593,430	PAMR1, METTL15, 128 more genes
nsv6638023	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 31,372,721-38,259,316 , GRCh38.p12 chr11: 31,351,174-38,237,766	PAMR1, THEM7P, 92 more genes
nsv3893233	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576	PAMR1, LOC105376598, 2842 more genes
nsv3900144	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169	PAMR1, RTN3, 2833 more genes
nsv3908873	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576	PAMR1, IGHMBP2, 2829 more genes
nsv6315537	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576	PAMR1, PYGM, 2125 more genes
nsv3898926	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-37,698,540 , GRCh38.p12 chr11: 230,615-37,676,990	PAMR1, OR51L1, 771 more genes
nsv3923805	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 34,161,694-36,799,127 , GRCh37 chr11: 34,183,241-36,820,677 , NCBI36 chr11: 34,139,817-36,777,253	PAMR1, PDHX, 39 more genes
nsv3920531	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr11: 35,081,341-38,769,618 , GRCh37 chr11: 35,124,765-38,813,042 , GRCh38 chr11: 35,103,218-38,791,492	PAMR1, DNAAF11P1, 30 more genes
nsv3907644	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 35,126,357-38,814,431 , GRCh38.p12 chr11: 35,104,810-38,792,881	PAMR1, LOC105376632, 30 more genes
nsv3921953	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr11: 35,135,480-37,649,168 , NCBI36 chr11: 35,113,603-37,627,294 , GRCh37 chr11: 35,157,027-37,670,718	PAMR1, LOC100422241, 23 more genes
nsv3896459	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 32,782,607-36,404,823 , GRCh38.p12 chr11: 32,761,061-36,383,273	PAMR1, HIPK3, 58 more genes
nsv4455656	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 34,183,318-36,860,753 , GRCh38.p12 chr11: 34,161,771-36,839,203	PAMR1, LOC102723568, 39 more genes
nsv3893968	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 34,189,942-36,857,171 , GRCh38.p12 chr11: 34,168,395-36,835,621	PAMR1, SNORD164, 39 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

Page of 2

Number of Variants: 20

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Supplemental Content

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Search details

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