nrg3[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
nsv3895399	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr10: 84,232,776-84,392,016 , GRCh38.p12 chr10: 82,473,020-82,632,260	NRG3
nsv3922078	copy number variation	1	nstd102	human	Benign	NCBI36 chr10: 84,127,655-84,259,988 , GRCh38 chr10: 82,377,919-82,510,252 , GRCh37 chr10: 84,137,675-84,270,008	NRG3
nsv3899395	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 84,173,117-84,255,527 , GRCh38.p12 chr10: 82,413,361-82,495,771	NRG3
nsv3901278	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 84,263,480-84,336,472 , GRCh38.p12 chr10: 82,503,724-82,576,716	NRG3
nsv3897804	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 84,136,681-84,206,002 , GRCh38.p12 chr10: 82,376,925-82,446,246	NRG3
nsv3897985	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 84,138,996-84,191,076 , GRCh38.p12 chr10: 82,379,240-82,431,320	NRG3
nsv3898922	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 84,134,206-84,186,263 , GRCh38.p12 chr10: 82,374,450-82,426,507	NRG3
nsv3898109	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 84,136,681-84,183,571 , GRCh38.p12 chr10: 82,376,925-82,423,815	NRG3
nsv3892718	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 84,128,059-84,173,117 , GRCh38.p12 chr10: 82,368,303-82,413,361	NRG3
nsv3911857	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr10: 84,541,102-84,561,595 , GRCh38 chr10: 82,781,346-82,801,839 , NCBI36 chr10: 84,531,082-84,551,575	NRG3
nsv3891993	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 83,942,004-83,959,179 , GRCh38.p12 chr10: 82,182,248-82,199,423	NRG3
nsv3902567	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 83,884,894-83,900,439 , GRCh38.p12 chr10: 82,125,138-82,140,683	NRG3
nsv3896222	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 84,127,899-84,136,681 , GRCh38.p12 chr10: 82,368,143-82,376,925	NRG3
nsv3892256	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 83,632,817-83,635,137 , GRCh38.p12 chr10: 81,873,061-81,875,381	NRG3
nsv3905428	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 84,128,008-84,129,637 , GRCh38.p12 chr10: 82,368,252-82,369,881	NRG3
nsv3901777	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 83,634,147-83,635,137 , GRCh38.p12 chr10: 81,874,391-81,875,381	NRG3
nsv3895758	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 83,634,171-83,635,137 , GRCh38.p12 chr10: 81,874,415-81,875,381	NRG3
nsv3900560	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 83,634,371-83,635,137 , GRCh38.p12 chr10: 81,874,615-81,875,381	NRG3
nsv3900584	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 84,232,776-84,433,985 , GRCh38.p12 chr10: 82,473,020-82,674,229	NRG3
nsv3906333	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 84,570,188-84,708,439 , GRCh38.p12 chr10: 82,810,432-82,948,683	NRG3

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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 102

Page of 6

Number of Variants: 20

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Supplemental Content

Find related data

Search details

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