ankmy2[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
nsv3892495	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 16,666,301-16,666,759 , GRCh38.p12 chr7: 16,626,676-16,627,134	ANKMY2
nsv6636686	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 16,669,990-16,784,421 , GRCh38.p12 chr7: 16,630,365-16,744,796	ANKMY2, BZW2
nsv3885046	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 16,348,148-16,729,531 , GRCh38 chr7: 16,308,523-16,689,906	ANKMY2, SOSTDC1, 6 more genes
nsv3919826	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840	ANKMY2, RNU6-438P, 2682 more genes
nsv3888815	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467	ANKMY2, LOC107986817, 2014 more genes
nsv3915219	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,649,696-25,800,180 , GRCh38 chr7: 10,610,069-25,760,560 , NCBI36 chr7: 10,616,221-25,766,705	ANKMY2, SNORD93, 176 more genes
nsv6313854	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 9,358,316-20,982,082 , GRCh38.p12 chr7: 9,318,686-20,942,463	ANKMY2, LOC107986766, 115 more genes
nsv3913922	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 9,975,653-19,356,878 , NCBI36 chr7: 9,981,805-19,363,026 , GRCh37 chr7: 10,015,280-19,396,501	ANKMY2, NPM1P13, 86 more genes
nsv3911741	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 15,573,437-24,891,051 , GRCh38 chr7: 15,533,812-24,851,432 , NCBI36 chr7: 15,539,962-24,857,576	ANKMY2, LINC01162, 124 more genes
nsv3912345	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 8,962,614-17,387,487 , GRCh37.p13 chr7: 8,996,089-17,420,962 , GRCh38.p12 chr7: 8,956,459-17,381,338	ANKMY2, RAD17P1, 78 more genes
nsv4674987	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 13,886,653-20,267,202 , GRCh38.p12 chr7: 13,847,028-20,227,579	ANKMY2, BZW2, 64 more genes
nsv4768371	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 14,470,668-20,385,165 , GRCh38.p12 chr7: 14,431,043-20,345,542	ANKMY2, HDAC9, 60 more genes
nsv3910744	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 15,133,711-19,642,829 , GRCh37 chr7: 15,173,336-19,682,452 , NCBI36 chr7: 15,139,861-19,648,977	ANKMY2, LOC105375171, 44 more genes
nsv3922488	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 16,161,141-20,647,522 , GRCh38 chr7: 16,121,516-20,607,899 , NCBI36 chr7: 16,127,666-20,614,047	ANKMY2, HDAC9, 53 more genes
nsv3912914	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 14,005,822-18,360,977 , GRCh38 chr7: 13,966,197-18,321,354 , NCBI36 chr7: 13,972,347-18,327,502	ANKMY2, RPL36AP26, 43 more genes
nsv3915495	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 14,911,044-16,931,243 , GRCh38 chr7: 14,904,894-16,925,094 , GRCh37 chr7: 14,944,519-16,964,718	ANKMY2, BZW2, 23 more genes
nsv3894780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842	ANKMY2, RNU6-565P, 2684 more genes
nsv4455091	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017	ANKMY2, RPL23AP51, 2684 more genes
nsv3909087	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 44,935-159,126,310 , GRCh38.p12 chr7: 44,935-159,333,620	ANKMY2, MNX1-AS2, 2682 more genes
nsv3908592	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr7: 43,361-159,119,707 , GRCh38.p12 chr7: 43,361-159,327,017	ANKMY2, TRGV3, 2682 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 47

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Number of Variants: 20

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