cdkn2d[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
nsv3922964	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 10,319,474-13,777,860 , NCBI36 chr19: 10,291,150-13,749,674 , GRCh37 chr19: 10,430,150-13,888,674	CDKN2D, SWSAP1, 164 more genes
nsv3922999	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 10,240,071-12,946,266 , GRCh37.p13 chr19: 10,379,071-13,085,266 , GRCh38.p12 chr19: 10,268,395-12,974,452	CDKN2D, ZNF433, 155 more genes
nsv3912242	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 9,846,119-11,338,677 , GRCh38 chr19: 9,735,443-11,228,001 , NCBI36 chr19: 9,707,119-11,199,677	CDKN2D, PPAN, 68 more genes
nsv3900924	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 10,286,133-11,040,457 , GRCh38.p12 chr19: 10,175,457-10,929,781	CDKN2D, MIR4322, 38 more genes
nsv3904885	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923	CDKN2D, ZNF321P, 2443 more genes
nsv3903203	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793	CDKN2D, BABAM1, 2426 more genes
nsv3903092	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521	CDKN2D, LENG8, 2408 more genes
nsv3898900	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 9,678,768-14,853,426 , GRCh38.p12 chr19: 9,568,092-14,742,614	CDKN2D, FBXL12, 253 more genes
nsv3923415	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 10,286,934-14,020,806 , GRCh37 chr19: 10,425,934-14,159,806 , GRCh38 chr19: 10,315,258-14,048,994	CDKN2D, MAN2B1, 182 more genes
nsv3920643	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 10,267,082-11,000,364 , NCBI36 chr19: 10,128,082-10,861,364 , GRCh38 chr19: 10,156,406-10,889,688	CDKN2D, MIR4748, 36 more genes
nsv3922509	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr19: 10,302,331-10,892,228 , GRCh37 chr19: 10,441,331-11,031,228 , GRCh38 chr19: 10,330,655-10,920,552	CDKN2D, DNM2, 26 more genes
nsv3920616	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr19: 8,802,823-13,303,041 , GRCh37 chr19: 8,941,823-13,442,041 , GRCh38 chr19: 8,831,147-13,331,227	CDKN2D, ACP5, 236 more genes
nsv4685775	copy number variation	1	nstd102	human	not provided	GRCh37 chr19: 10,642,984-12,810,067 , GRCh38.p12 chr19: 10,532,308-12,699,253	CDKN2D, SLC44A2, 114 more genes
nsv4451686	copy number variation	1	nstd102	human	not provided	GRCh37 chr19: 10,642,984-12,810,067 , GRCh38.p12 chr19: 10,532,308-12,699,253	CDKN2D, ODAD3, 114 more genes
nsv4457721	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 10,441,330-10,977,962 , GRCh38.p12 chr19: 10,330,654-10,867,286	CDKN2D, QTRT1, 24 more genes
nsv6291543	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 9,941,033-11,739,567 , GRCh38.p12 chr19: 9,830,357-11,628,752	CDKN2D, KRI1, 88 more genes
nsv4676283	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 10,632,623-11,135,294 , GRCh38.p12 chr19: 10,521,947-11,024,618	CDKN2D, ATG4D, 21 more genes
nsv3905293	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 10,584,393-10,938,252 , GRCh38.p12 chr19: 10,473,717-10,827,576	CDKN2D, MIR638, 16 more genes
nsv7098944	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 10,624,491-10,969,019 , GRCh38.p12 chr19: 10,513,815-10,858,343	CDKN2D, DNM2, 17 more genes

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cdkn2d[All Fields] AND 1[has_clinical] (20)
dbVar
NIH_XGC_tropTad5
NIH_XGC_tropTad5

biosample
BioSample links for Nucleotide (Select 74282572) (1)
BioSample

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