tceanc2[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 14

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Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4768338	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 53,675,707-66,644,963 , GRCh38.p12 chr1: 53,210,035-66,179,280	TCEANC2, TALDO1P1, 201 more genes
nsv3895522	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 54,092,945-64,714,537 , GRCh38 chr1: 53,627,272-64,248,854 , NCBI36 chr1: 53,865,533-64,487,125	TCEANC2, FGGY, 159 more genes
nsv3893402	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 53,738,212-61,439,648 , NCBI36 chr1: 53,976,473-61,677,908 , GRCh37 chr1: 54,203,885-61,905,320	TCEANC2, LOC105378748, 107 more genes
nsv5381135	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 51,941,877-56,688,514 , GRCh38.p12 chr1: 51,476,205-56,222,842	TCEANC2, LRP8-DT, 122 more genes
nsv3871136	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 51,729,573-55,164,001 , GRCh38.p12 chr1: 51,263,901-54,698,328	TCEANC2, MROH7, 100 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	TCEANC2, 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	TCEANC2, 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	TCEANC2, RNU1-153P, 4887 more genes
nsv3896927	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 53,061,024-77,233,450 , GRCh38 chr1: 52,595,352-76,767,765 , NCBI36 chr1: 52,833,612-77,006,038	TCEANC2, DNAI4, 346 more genes
nsv3899721	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr1: 53,025,763-67,578,144 , GRCh37 chr1: 53,253,175-67,805,556 , GRCh38 chr1: 52,787,503-67,339,873	TCEANC2, AK4, 230 more genes
nsv3872198	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 54,575,439-55,381,546 , GRCh38.p12 chr1: 54,109,766-54,915,873	TCEANC2, CDCP2, 18 more genes
nsv4436181	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532	TCEANC2, LINC01776, 1853 more genes
nsv4453879	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 54,002,963-54,575,440 , GRCh38.p12 chr1: 53,537,290-54,109,767	TCEANC2, MIR4781, 12 more genes
nsv3907097	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 54,289,408-54,793,786 , GRCh38 chr1: 53,823,735-54,328,113 , NCBI36 chr1: 54,061,996-54,566,374	TCEANC2, RPL37P7, 15 more genes

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