dnhd1[All Fields] AND 1[has_clinical] - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv5672634	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 6,559,613-6,640,631 , GRCh38.p12 chr11: 6,538,383-6,619,400	DNHD1, TPP1, 4 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	DNHD1, 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	DNHD1, 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	DNHD1, IGHMBP2, 2829 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	DNHD1, OR51L1, 771 more genes
nsv4674879	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449	DNHD1, BGLT3, 723 more genes
nsv3906221	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-31,995,219 , GRCh38.p12 chr11: 230,615-31,973,673	DNHD1, PCNAP4, 688 more genes
nsv6315535	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599	DNHD1, OR52Q1P, 630 more genes
nsv3894525	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-25,584,362 , GRCh38.p12 chr11: 230,615-25,562,816	DNHD1, SDHCP4, 620 more genes
nsv3912558	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 446,754-18,926,289 , GRCh38 chr11: 446,754-18,904,742 , NCBI36 chr11: 436,754-18,882,865	DNHD1, TRIM22, 546 more genes
nsv3898948	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-17,099,213 , GRCh38.p12 chr11: 230,615-17,077,666	DNHD1, MTND5P21, 506 more genes
nsv4350476	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 193,146-12,643,136 , GRCh38.p12 chr11: 193,146-12,621,589	DNHD1, KRTAP5-3, 457 more genes
nsv3919565	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 61,793-10,727,969 , GRCh37 chr11: 61,793-10,749,516 , NCBI36 chr11: 51,793-10,706,092	DNHD1, OR51A7, 437 more genes
nsv3892294	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-9,704,511 , GRCh38.p12 chr11: 230,615-9,682,964	DNHD1, MRPS24P1, 405 more genes
nsv4768373	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811	DNHD1, LOC107984302, 375 more genes
nsv6637864	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177	DNHD1, PNPLA2, 372 more genes
nsv3915725	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 6,239,388-6,615,806 , GRCh38 chr11: 6,261,582-6,637,999 , GRCh37 chr11: 6,282,812-6,659,230	DNHD1, TRIM3, 14 more genes
nsv4681173	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr11: 5,709,028-6,640,651 , GRCh38.p12 chr11: 5,687,798-6,619,420	DNHD1, OR56B2P, 50 more genes
nsv4456235	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 5,896,551-6,719,852 , GRCh38.p12 chr11: 5,875,321-6,698,621	DNHD1, OR52X1P, 40 more genes
nsv6290772	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 6,502,523-7,248,333 , GRCh38.p12 chr11: 6,481,293-7,227,102	DNHD1, GVINP2, 26 more genes

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

Send to:

Search results

Items: 1 to 20 of 21

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Search details

Recent activity

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

Page of 2

Supplemental Content

Find related data

Search details

Recent activity