tnnt2[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
nsv5381065	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 201,334,309-201,342,392 , GRCh38.p12 chr1: 201,365,181-201,373,264	TNNT2
nsv6310774	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 201,327,136-201,347,828 , GRCh38.p12 chr1: 201,358,008-201,378,700	TNNT2
nsv7095776	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 201,328,338-201,342,382 , GRCh38.p12 chr1: 201,359,210-201,373,254	TNNT2
nsv3910054	delins	1	nstd102	human	Uncertain significance	GRCh38 chr1: 201,362,042-201,362,067 , GRCh37 chr1: 201,331,170-201,331,195	TNNT2
nsv3912840	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 144,764,751-247,199,719 , GRCh37.p13 chr1: 146,053,394-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643	TNNT2, CRB1, 1608 more genes
nsv3888143	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 179,413,479-201,764,737 , GRCh38.p12 chr1: 179,444,344-201,795,609	TNNT2, CSRP1-AS1, 273 more genes
nsv3901050	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 200,144,603-203,112,078 , NCBI36 chr1: 198,380,354-201,347,829 , GRCh37 chr1: 200,113,731-203,081,206	TNNT2, IPO9, 80 more genes
nsv3877365	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250	TNNT2, MARK1, 4930 more genes
nsv3885206	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793	TNNT2, SNAP47, 4927 more genes
nsv3884414	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485	TNNT2, RNU1-153P, 4887 more genes
nsv3918947	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 144,475,856-247,199,719 , GRCh37.p13 chr1: 145,764,499-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643	TNNT2, LOC101060227, 1608 more genes
nsv4450583	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 182,388,773-249,111,240 , GRCh38.p12 chr1: 182,419,638-248,817,041	TNNT2, RGS18, 1186 more genes
nsv3881012	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 195,483,439-249,213,000 , GRCh38.p12 chr1: 195,514,309-248,918,801	TNNT2, LOC105372928, 1062 more genes
nsv6634372	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485	TNNT2, LOC105373279, 1036 more genes
nsv3895767	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 187,143,981-224,299,417 , NCBI36 chr1: 185,379,736-222,553,742 , GRCh37 chr1: 187,113,113-224,487,119	TNNT2, LOC107985458, 590 more genes
nsv3889347	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 185,644,663-221,698,833 , GRCh38.p12 chr1: 185,675,531-221,525,491	TNNT2, MIR1231, 543 more genes
nsv6636965	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 181,453,460-213,107,248 , GRCh38.p12 chr1: 181,484,324-212,933,906	TNNT2, PRELP, 527 more genes
nsv3879807	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 197,811,907-228,997,888 , GRCh38.p12 chr1: 197,842,777-228,862,141	TNNT2, RABIF, 637 more genes
nsv3916948	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr1: 199,268,692-199,633,333 , GRCh37.p13 chr1: 201,002,069-201,366,710 , GRCh38.p12 chr1: 201,032,941-201,397,582	TNNT2, CACNA1S, 7 more genes
nsv3922179	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr1: 199,509,694-200,143,215 , GRCh37.p13 chr1: 201,243,071-201,876,592 , GRCh38.p12 chr1: 201,273,943-201,907,464	TNNT2, CSRP1, 17 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 26

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 26

Page of 2

Number of Variants: 20

Page of 2

Supplemental Content

Find related data

Search details

Recent activity