katnal2[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
nsv3911957	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr18: 46,923,513-46,959,260 , NCBI36 chr18: 42,757,474-42,793,221 , GRCh37 chr18: 44,503,476-44,539,223	KATNAL2
nsv3922390	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr18: 42,818,178-42,845,860 , GRCh38 chr18: 47,037,809-47,065,491 , GRCh37 chr18: 44,564,180-44,591,862	KATNAL2
nsv4457802	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr18: 44,523,868-44,539,223 , GRCh38.p12 chr18: 46,943,905-46,959,260	KATNAL2
nsv3896170	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr18: 44,523,938-44,539,223 , GRCh38.p12 chr18: 46,943,975-46,959,260	KATNAL2
nsv3909864	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr18: 42,812,147-42,822,900 , GRCh37 chr18: 44,558,149-44,568,902 , GRCh38 chr18: 47,031,778-47,042,531	KATNAL2, ELOA2
nsv3921228	copy number variation	1	nstd102	human	Benign	NCBI36 chr18: 42,814,398-42,815,895 , GRCh37 chr18: 44,560,400-44,561,897 , GRCh38 chr18: 47,034,029-47,035,526	KATNAL2, ELOA2
nsv3896591	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr18: 44,564,162-44,619,806 , GRCh38.p12 chr18: 47,037,791-47,093,435	KATNAL2, LOC105372098
nsv4457425	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr18: 44,575,514-44,614,090 , GRCh38.p12 chr18: 47,049,143-47,087,719	KATNAL2, LOC105372098
nsv3887147	copy number variation	1	nstd102	human	Likely pathogenic	GRCh38 chr18: 47,026,162-47,075,742 , GRCh37.p13 chr18: 44,552,533-44,602,113	KATNAL2, ELOA2, 2 more genes
nsv3898734	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr18: 44,524,612-44,546,715 , GRCh38.p12 chr18: 46,944,649-46,966,752	KATNAL2, ELOA3DP, 1 more genes
nsv6291497	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr18: 44,552,943-44,605,249 , GRCh38.p12 chr18: 47,026,572-47,078,878	KATNAL2, ELOA2, 2 more genes
nsv3898362	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr18: 44,615,320-44,644,887 , GRCh38.p12 chr18: 47,088,949-47,118,516	KATNAL2, HDHD2, 1 more genes
nsv3896338	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr18: 44,564,161-44,655,843 , GRCh38.p12 chr18: 47,037,790-47,129,472	KATNAL2, HDHD2, 1 more genes
nsv6314722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 1,262,334-53,254,751 , GRCh38.p12 chr18: 1,262,333-55,587,520	KATNAL2, LOC107985176, 632 more genes
nsv3911609	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr18: 36,859,191-47,164,436 , GRCh37 chr18: 34,439,154-44,690,807 , NCBI36 chr18: 32,693,152-42,944,805	KATNAL2, MIR4319, 91 more genes
nsv3923799	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr18: 41,722,823-49,043,887 , GRCh37 chr18: 39,302,787-46,570,257 , NCBI36 chr18: 37,556,785-44,824,255	KATNAL2, RNU6-1278P, 81 more genes
nsv4676219	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 41,630,585-45,107,905 , GRCh38.p12 chr18: 44,050,620-47,581,534	KATNAL2, HAUS1, 48 more genes
nsv6315530	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271	KATNAL2, LOC105372145, 947 more genes
nsv3907444	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 12,842-78,015,180 , GRCh38.p12 chr18: 12,842-80,257,297	KATNAL2, GALNT1, 947 more genes
nsv3890669	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 13,034-78,015,180 , GRCh38.p12 chr18: 13,034-80,257,297	KATNAL2, MYL12B, 947 more genes

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Number of Variants: 20

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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 63

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Number of Variants: 20

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