ttll9[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
nsv3892750	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,961,294 , GRCh38.p12 chr20: 82,603-64,329,941	TTLL9, TGIF2-RAB5IF, 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	TTLL9, LRRN4, 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	TTLL9, PKIG, 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	TTLL9, COMMD7, 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	TTLL9, MIR3646, 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	TTLL9, DYNLRB1, 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	TTLL9, KIF3B, 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	TTLL9, MYH7B, 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	TTLL9, LOC105372586, 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	TTLL9, EFCAB8, 162 more genes
nsv3917138	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 31,254,983-33,473,080 , NCBI36 chr20: 29,306,447-31,524,547 , GRCh37 chr20: 29,842,786-32,060,886	TTLL9, HAUS6P2, 78 more genes
nsv3912259	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 31,254,983-32,575,288 , NCBI36 chr20: 29,306,447-30,626,751 , GRCh37 chr20: 29,842,786-31,163,090	TTLL9, RNA5SP482, 51 more genes
nsv6291578	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr20: 18,665,879-33,903,216 , GRCh38.p12 chr20: 18,685,235-35,315,413	TTLL9, AHCY, 330 more genes
nsv4729757	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr20: 19,750,804-30,479,077 , GRCh38.p12 chr20: 19,770,160-31,891,274	TTLL9, BCL2L1, 222 more genes
nsv3897443	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr20: 24,162,775-31,820,857 , GRCh38.p12 chr20: 24,182,139-33,233,051	TTLL9, BCL2L1, 165 more genes
nsv6637546	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr20: 29,652,122-35,603,726 , GRCh38.p12 chr20: 30,417,446-36,975,323	TTLL9, AHCY, 195 more genes
nsv6637725	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr20: 29,833,535-34,815,537 , GRCh38.p12 chr20: 31,245,732-36,227,615	TTLL9, AHCY, 160 more genes
nsv3922338	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr20: 29,297,047-30,068,749 , GRCh37 chr20: 29,833,386-30,605,088 , GRCh38 chr20: 31,245,583-32,017,285	TTLL9, BCL2L1, 38 more genes
nsv6291628	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr20: 30,239,509-30,494,851 , GRCh38.p12 chr20: 31,651,706-31,907,048	TTLL9, BCL2L1, 7 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 27

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 27

Page of 2

Number of Variants: 20

Page of 2

Supplemental Content

Find related data

Search details

Recent activity