rela[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
nsv7094008	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 65,429,138-65,430,303 , GRCh38.p12 chr11: 65,661,667-65,662,832	RELA, RELA-DT
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	RELA, FAUP4, 2031 more genes
nsv6309121	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr11: 64,522,783-66,283,694 , GRCh38.p12 chr11: 64,755,311-66,516,223	RELA, SF3B2, 124 more genes
nsv7093933	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr11: 65,325,080-65,639,825 , GRCh38.p12 chr11: 65,557,609-65,872,354	RELA, ZNRD2-DT, 22 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	RELA, 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	RELA, 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	RELA, 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	RELA, PYGM, 2125 more genes
nsv3892750	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,961,294 , GRCh38.p12 chr20: 82,603-64,329,941	TGIF2-RAB5IF, LOC105372609, 1314 more genes
nsv3905072	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,948,788 , GRCh38.p12 chr20: 82,603-64,317,435	LRRN4, SNRPB, 1313 more genes
nsv3895314	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr20: 61,569-62,915,555 , GRCh38.p12 chr20: 80,928-64,284,202	PKIG, LINC01523, 1311 more genes
nsv3896520	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,912,463 , GRCh38.p12 chr20: 82,603-64,281,110	COMMD7, RNU7-6P, 1311 more genes
nsv3920218	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118	MIR3646, NPEPL1, 1310 more genes
nsv3910142	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 9,792,081-37,945,599 , GRCh38 chr20: 9,811,433-39,316,956 , NCBI36 chr20: 9,740,081-37,379,013	DYNLRB1, LOC107985402, 555 more genes
nsv3904899	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 17,705,775-31,600,738 , GRCh38.p12 chr20: 17,725,130-33,012,932	TTLL9, ABHD12, 297 more genes
nsv3878906	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 17,705,775-31,600,738 , GRCh38.p12 chr20: 17,725,130-33,012,932	KIF3B, GINS1, 297 more genes
nsv3918053	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 25,703,100-38,491,480 , GRCh37.p13 chr20: 25,755,100-39,058,066 , GRCh38.p12 chr20: 25,774,464-40,429,426	MYH7B, PPP1R16B, 300 more genes
nsv6313956	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 25,442,597-33,761,550 , GRCh38.p12 chr20: 25,461,961-35,173,747	LOC105372586, RNU6-384P, 193 more genes
nsv4457806	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 29,833,608-35,087,952 , GRCh38.p12 chr20: 31,245,805-36,459,549	EFCAB8, C20orf203, 162 more genes
nsv4349000	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 65,138,976-67,574,402 , GRCh38.p12 chr11: 65,371,505-67,806,931	RELA, SNORD13F, 141 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 55

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 55

Page of 3

Number of Variants: 20

Page of 3

Supplemental Content

Find related data

Search details

Recent activity