app[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
nsv3893030	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 58,579,726-58,580,231 , GRCh38.p12 chr17: 60,502,365-60,502,870	APPBP2
nsv3895219	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr21: 27,321,237-27,477,404 , GRCh38.p12 chr21: 25,948,923-26,105,087	APP
nsv3895764	copy number variation	1	nstd102	human	Benign	GRCh37 chr21: 27,361,704-27,437,496 , GRCh38.p12 chr21: 25,989,391-26,065,180	APP
nsv3918696	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr21: 26,089,149-26,145,977 , NCBI36 chr21: 26,383,336-26,440,166 , GRCh37 chr21: 27,461,465-27,518,295	APP
nsv3910260	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr21: 26,373,320-26,402,096 , GRCh37.p13 chr21: 27,451,449-27,480,225 , GRCh38.p12 chr21: 26,079,133-26,107,909	APP
nsv6311063	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr21: 27,253,981-27,277,409 , GRCh38.p12 chr21: 25,881,670-25,905,097	APP
nsv4729824	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr21: 27,469,388-27,490,099 , GRCh38.p12 chr21: 26,097,071-26,117,782	APP
nsv7148058	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr21: 26,076,967-26,097,154 , GRCh37.p13 chr21: 27,449,283-27,469,471	APP
nsv3910658	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr21: 26,250,729-26,467,584 , GRCh37.p13 chr21: 27,328,858-27,545,713 , GRCh38.p12 chr21: 25,956,544-26,173,395	APP
nsv6311104	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr21: 27,462,239-27,542,938 , GRCh38.p12 chr21: 26,089,923-26,170,620	APP
nsv6636052	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr21: 27,484,473-27,542,948 , GRCh38.p12 chr21: 26,112,156-26,170,630	APP
nsv3913286	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr21: 25,879,180-25,896,618 , NCBI36 chr21: 26,173,362-26,190,801 , GRCh37 chr21: 27,251,491-27,268,930	APP
nsv6311157	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr21: 27,251,861-27,544,138 , GRCh38.p12 chr21: 25,879,550-26,171,820	APP, RNU6-123P
nsv6636159	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr21: 27,253,971-27,542,948 , GRCh38.p12 chr21: 25,881,660-26,170,630	APP, RNU6-123P
nsv6637412	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr21: 27,288,136-27,397,444 , GRCh38.p12 chr21: 25,915,824-26,025,128	APP, RNU6-123P
nsv3911811	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577	PRPSAP1, CACNG1, 1350 more genes
nsv3923176	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr21: 7,817,158-46,670,440 , NCBI36 chr21: 14,406,909-46,914,780 , GRCh37 chr21: 15,485,038-48,090,352	APP, COL18A1-AS2, 682 more genes
nsv3905423	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr21: 15,538,655-48,080,926 , GRCh38.p12 chr21: 14,166,334-46,661,014	APP, MTND5P1, 581 more genes
nsv3917693	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr21: 7,749,532-37,653,653 , GRCh37 chr21: 15,451,032-39,025,955 , NCBI36 chr21: 14,372,903-37,947,825	APP, DPRXP5, 448 more genes
nsv3922838	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr21: 10,366,915-27,611,416 , GRCh37.p13 chr21: 14,338,130-28,983,735	APP, RN7SL163P, 178 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 110

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Number of Variants: 20

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