katnip[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
nsv7094778	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 27,712,890-27,713,036 , GRCh38.p12 chr16: 27,701,569-27,701,715	KATNIP
nsv4456221	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr16: 27,599,138-27,681,983 , GRCh38.p12 chr16: 27,587,817-27,670,662	KATNIP, LOC107984874
nsv4457087	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 27,456,568-27,573,237 , GRCh38.p12 chr16: 27,445,247-27,561,916	KATNIP, IL21R, 2 more genes
nsv4675848	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 27,524,212-27,758,777 , GRCh38.p12 chr16: 27,512,891-27,747,456	KATNIP, LOC107984874, 3 more genes
nsv4455712	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 27,524,212-27,749,983 , GRCh38.p12 chr16: 27,512,891-27,738,662	KATNIP, GTF3C1, 2 more genes
nsv7094831	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 27,561,492-27,733,036 , GRCh38.p12 chr16: 27,550,171-27,721,715	KATNIP, GTF3C1, 2 more genes
nsv3905855	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 21,596,299-30,399,167 , GRCh38.p12 chr16: 21,584,978-30,387,846	KATNIP, LOC107984874, 217 more genes
nsv6290289	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 21,594,997-29,625,302 , GRCh38.p12 chr16: 21,583,676-29,613,981	KATNIP, LOC105371149, 166 more genes
nsv3891271	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 21,379,628-29,379,768 , GRCh38.p12 chr16: 21,368,307-29,368,447	KATNIP, LOC101927814, 159 more genes
nsv6289847	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 21,530,207-29,332,245 , GRCh38.p12 chr16: 21,518,886-29,320,924	KATNIP, GAPDHP35, 154 more genes
nsv7137115	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 21,467,726-29,044,717 , GRCh38.p12 chr16: 21,456,405-29,033,396	KATNIP, OTOAP1, 148 more genes
nsv3924349	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 21,612,313-28,334,665 , GRCh38 chr16: 21,600,992-28,323,344 , NCBI36 chr16: 21,519,814-28,242,166	KATNIP, SLC5A11, 111 more genes
nsv7094777	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 27,441,393-29,001,333 , GRCh38.p12 chr16: 27,430,072-28,990,012	KATNIP, NUPR1, 45 more genes
nsv3906108	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224	KATNIP, CKLF, 1882 more genes
nsv3904593	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973	KATNIP, LOC100128079, 1879 more genes
nsv3901410	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287	KATNIP, LINC02175, 1877 more genes
nsv3909417	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867	KATNIP, PRSS53, 1868 more genes
nsv3892266	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654	KATNIP, FTLP14, 1868 more genes
nsv4685985	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 5,805,001-34,230,001 , GRCh38.p12 chr16: 5,755,000-34,995,630	KATNIP, LOC105371069, 654 more genes
nsv1398297	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 102,839-28,327,676 , GRCh38.p12 chr16: 52,839-28,316,355	KATNIP, BMERB1, 701 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 47

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Number of Variants: 20

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