ark2n[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
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	ARK2N, 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	ARK2N, 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	ARK2N, RNU6-1278P, 81 more genes
nsv4676156	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 39,800,804-44,365,152 , GRCh38.p12 chr18: 42,220,839-46,785,189	ARK2N, LOC105372089, 40 more genes
nsv3921955	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 38,169,137-42,560,421 , GRCh38 chr18: 42,335,174-46,726,460 , GRCh37 chr18: 39,915,139-44,306,423	ARK2N, ATP5F1A, 38 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	ARK2N, HAUS1, 48 more genes
nsv7095444	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 42,281,312-44,236,996 , GRCh38.p12 chr18: 44,701,347-46,657,033	ARK2N, HAUS1, 21 more genes
nsv6315530	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271	ARK2N, 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	ARK2N, 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	ARK2N, MYL12B, 947 more genes
nsv3918488	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 43,345-76,068,860 , GRCh38 chr18: 53,345-80,209,986 , GRCh37 chr18: 53,345-77,967,869	ARK2N, LOC105372027, 945 more genes
nsv3924351	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 108,760-76,113,817 , GRCh38 chr18: 118,760-80,254,946 , GRCh37 chr18: 118,760-78,012,829	ARK2N, MIX23P1, 942 more genes
nsv3919004	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr18: 136,226-80,256,240 , GRCh37 chr18: 136,226-78,014,123 , NCBI36 chr18: 126,226-76,115,097	ARK2N, LIVAR, 941 more genes
nsv3899451	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 136,226-78,014,123 , GRCh38.p12 chr18: 136,226-80,256,240	ARK2N, BOLA2P1, 941 more genes
nsv3924706	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 136,227-78,014,123 , GRCh38 chr18: 136,227-80,256,240 , NCBI36 chr18: 126,227-76,115,097	ARK2N, LOC100420948, 941 more genes
nsv3907722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 136,227-78,014,123 , GRCh38.p12 chr18: 136,227-80,256,240	ARK2N, ROCK1, 941 more genes
nsv3910887	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 139,089-76,113,807 , GRCh37 chr18: 149,089-78,012,819 , GRCh38 chr18: 149,089-80,254,936	ARK2N, LPIN2, 941 more genes
nsv3912925	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr18: 138,963-76,111,023 , GRCh38 chr18: 148,963-80,252,149 , GRCh37 chr18: 148,963-78,010,032	ARK2N, LOC105372038, 941 more genes
nsv3923838	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 138,963-76,103,255 , GRCh37 chr18: 148,963-78,002,264 , GRCh38 chr18: 148,963-80,244,381	ARK2N, WDR7-OT1, 941 more genes
nsv3916426	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 149,089-77,992,274 , NCBI36 chr18: 139,089-76,093,265 , GRCh38 chr18: 149,089-80,234,391	ARK2N, TPGS2, 941 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 45

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Number of Variants: 20

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Supplemental Content

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