pkn2[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 19

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Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3888313	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 89,079,544-89,096,946 , GRCh38.p12 chr1: 88,613,861-88,631,263	LOC105378838, PKN2-AS1
nsv3887845	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 89,094,540-89,102,071 , GRCh38.p12 chr1: 88,628,857-88,636,388	LOC105378838, PKN2-AS1
nsv3871978	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 89,094,540-89,096,946 , GRCh38.p12 chr1: 88,628,857-88,631,263	PKN2-AS1, LOC105378838
nsv3903596	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr1: 88,166,589-88,798,176 , GRCh37 chr1: 88,394,001-89,025,588 , GRCh38 chr1: 87,928,318-88,559,905	LOC105378839, RN7SL583P, 3 more genes
nsv3918910	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr1: 88,923,777-89,119,326 , GRCh37.p13 chr1: 89,151,189-89,346,738 , GRCh38.p12 chr1: 88,685,506-88,881,055	PKN2, GTF2B, 3 more genes
nsv6313574	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 68,180,293-92,731,957 , GRCh38.p12 chr1: 67,714,610-92,266,400	PKN2, RNA5SP51, 315 more genes
nsv3885743	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 72,044,544-92,505,091 , GRCh38.p12 chr1: 71,578,861-92,039,534	PKN2, ZNHIT6, 257 more genes
nsv3905989	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 76,884,987-89,094,147 , NCBI36 chr1: 76,657,575-88,866,735 , GRCh38 chr1: 76,419,302-88,628,464	DNAJB4, SH3GLB1, 146 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	PKN2, 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	PKN2, 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	PKN2, RNU1-153P, 4887 more genes
nsv3898327	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 83,457,325-104,273,917 , GRCh37 chr1: 83,923,008-104,816,539 , NCBI36 chr1: 83,695,596-104,618,062	PKN2, LINC01773, 322 more genes
nsv4728566	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr1: 80,804,502-89,490,384 , GRCh38.p12 chr1: 80,338,817-89,024,701	PKN2, CLCA1, 103 more genes
nsv3881064	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 89,123,443-89,399,431 , GRCh38.p12 chr1: 88,657,760-88,933,748	PKN2, KYAT3, 5 more genes
nsv3918182	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr1: 88,517,230-88,939,649 , GRCh37.p13 chr1: 88,744,642-89,167,061 , GRCh38.p12 chr1: 88,278,959-88,701,378	PKN2, RPL36AP10, 4 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	PKN2, LINC01776, 1853 more genes
nsv3887791	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 88,840,026-89,512,154 , GRCh38.p12 chr1: 88,374,343-89,046,471	PKN2, ELOCP19, 12 more genes
nsv4452508	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 89,239,549-89,733,747 , GRCh38.p12 chr1: 88,773,866-89,268,064	PKN2, LOC107985076, 17 more genes
nsv4674604	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 89,018,909-89,483,015 , GRCh38.p12 chr1: 88,553,226-89,017,332	PKN2, PKN2-AS1, 9 more genes

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