tmem120a[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7097753	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 75,583,311-75,695,728 , GRCh38.p12 chr7: 75,953,993-76,066,410	TMEM120A, MDH2, 2 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	TMEM120A, RNU6-438P, 2682 more genes
nsv3888815	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467	TMEM120A, LOC107986817, 2014 more genes
nsv3918722	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 71,225,344-81,735,657 , GRCh37 chr7: 70,690,330-81,364,973 , NCBI36 chr7: 70,328,266-81,202,909	TMEM120A, GTF2IP1, 184 more genes
nsv3922762	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 73,992,744-83,618,176 , GRCh38 chr7: 73,873,420-83,988,860 , NCBI36 chr7: 72,925,686-83,456,112	TMEM120A, PMS2P3, 142 more genes
nsv3911276	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 69,382,353-77,823,832 , GRCh37 chr7: 68,847,339-77,453,149 , NCBI36 chr7: 68,485,275-77,291,085	TMEM120A, POM121, 155 more genes
nsv3917211	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 74,377,395-82,031,742 , NCBI36 chr7: 73,429,661-81,498,994 , GRCh37 chr7: 73,992,744-81,661,058	TMEM120A, HSPB1, 123 more genes
nsv3902523	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 75,588,704-80,277,632 , GRCh38.p12 chr7: 75,959,386-80,648,316	TMEM120A, GSAP, 72 more genes
nsv4728820	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 72,403,117-76,709,600 , GRCh38.p12 chr7: 72,932,579-77,080,283	TMEM120A, FDPSP7, 119 more genes
nsv6290688	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 75,058,300-79,083,658 , GRCh37.p13 chr7: 75,921,853-78,712,974	TMEM120A, GTF2IP1, 76 more genes
nsv3902539	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 72,456,604-76,007,380 , GRCh38.p12 chr7: 72,986,074-76,378,063	TMEM120A, WBSCR23, 97 more genes
nsv3922160	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 72,404,249-76,189,514 , GRCh38 chr7: 73,352,304-76,722,261 , GRCh37 chr7: 72,766,313-76,351,578	TMEM120A, PMS2P10, 88 more genes
nsv4675200	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 72,621,722-76,007,380 , GRCh38.p12 chr7: 73,207,682-76,378,063	TMEM120A, PHB1P15, 87 more genes
nsv4349368	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 72,744,494-76,038,818 , GRCh38.p12 chr7: 73,330,491-76,409,501	TMEM120A, MDH2, 83 more genes
nsv3921264	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 74,963,960-77,842,828 , GRCh37 chr7: 75,126,024-78,004,892 , GRCh38 chr7: 75,496,701-78,375,575	TMEM120A, PMS2P11, 56 more genes
nsv3912641	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 74,904,287-76,093,741 , GRCh37.p13 chr7\|NW_003871064.1: 2,966,309-3,821,770 , GRCh37.p13 chr7: 75,066,351-76,255,805 , GRCh38.p12 chr7: 75,437,073-76,626,488	TMEM120A, YWHAG, 29 more genes
nsv3924660	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 74,969,775-76,134,254 , GRCh37.p13 chr7\|NW_003871064.1: 3,031,751-3,821,770 , GRCh37.p13 chr7: 75,131,839-76,296,318 , GRCh38.p12 chr7: 75,502,515-76,667,001	TMEM120A, POMZP3, 28 more genes
nsv3921631	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 75,529,854-76,611,483 , GRCh37 chr7: 75,159,180-76,240,800 , NCBI36 chr7: 74,997,116-76,078,736	TMEM120A, SRRM3, 26 more genes
nsv3894780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842	TMEM120A, RNU6-565P, 2684 more genes
nsv4455091	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017	TMEM120A, RPL23AP51, 2684 more genes

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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 46

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Number of Variants: 20

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