mad1l1[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
nsv3901432	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 1,944,820-2,048,844 , GRCh38.p12 chr7: 1,905,184-2,009,209	MAD1L1
nsv3896599	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 1,944,591-2,048,335 , GRCh38.p12 chr7: 1,904,955-2,008,700	MAD1L1
nsv3906674	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 1,942,556-2,032,803 , GRCh38.p12 chr7: 1,902,920-1,993,168	MAD1L1
nsv3921526	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 1,958,233-2,032,641 , NCBI36 chr7: 1,924,759-1,999,167 , GRCh38 chr7: 1,918,597-1,993,006	MAD1L1
nsv3910407	copy number variation	1	nstd102	human	Benign	NCBI36 chr7: 1,973,885-2,041,488 , GRCh38 chr7: 1,967,724-2,035,327 , GRCh37 chr7: 2,007,359-2,074,962	MAD1L1
nsv3899382	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 1,987,092-2,048,844 , GRCh38.p12 chr7: 1,947,457-2,009,209	MAD1L1
nsv3897336	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 1,977,535-2,032,803 , GRCh38.p12 chr7: 1,937,899-1,993,168	MAD1L1
nsv3896129	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 1,977,664-2,032,803 , GRCh38.p12 chr7: 1,938,028-1,993,168	MAD1L1
nsv3909543	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 1,993,899-2,032,803 , GRCh38.p12 chr7: 1,954,264-1,993,168	MAD1L1
nsv3909238	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 2,017,445-2,050,535 , GRCh38.p12 chr7: 1,977,810-2,010,900	MAD1L1
nsv3908993	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 2,017,445-2,049,880 , GRCh38.p12 chr7: 1,977,810-2,010,245	MAD1L1
nsv3907468	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 2,030,440-2,050,535 , GRCh38.p12 chr7: 1,990,805-2,010,900	MAD1L1
nsv3894321	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 2,030,440-2,049,880 , GRCh38.p12 chr7: 1,990,805-2,010,245	MAD1L1
nsv3901111	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 2,030,442-2,039,594 , GRCh38.p12 chr7: 1,990,807-1,999,959	MAD1L1
nsv3892083	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 2,030,440-2,032,803 , GRCh38.p12 chr7: 1,990,805-1,993,168	MAD1L1
nsv4455271	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 2,166,170-2,189,394 , GRCh38.p12 chr7: 2,126,535-2,149,759	MAD1L1
nsv3900277	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 2,175,164-2,252,495 , GRCh38.p12 chr7: 2,135,529-2,212,860	MAD1L1, LOC105375126
nsv4675190	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr7: 1,989,321-2,171,115 , GRCh38.p12 chr7: 1,949,686-2,131,480	MAD1L1, SNORA114, 1 more genes
nsv4456500	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 1,835,893-2,021,563 , GRCh38.p12 chr7: 1,796,257-1,981,928	MAD1L1, MIR4655, 1 more genes
nsv3919826	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840	MAD1L1, RNU6-438P, 2682 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 75

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 75

Page of 4

Number of Variants: 20

Page of 4

Supplemental Content

Find related data

Search details

Recent activity