ncbp2[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
nsv3888413	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 196,663,447-196,678,885 , GRCh38.p12 chr3: 196,936,576-196,952,014	NCBP2, NCBP2AS2, 2 more genes
nsv3915488	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 185,203,637-197,837,049 , NCBI36 chr3: 186,686,331-199,321,446 , GRCh38 chr3: 185,485,849-198,110,178	NCBP2, SNAR-I, 260 more genes
nsv3872972	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 189,101,446-197,838,262 , GRCh38.p12 chr3: 189,383,657-198,111,391	NCBP2, TMEM44, 187 more genes
nsv6290259	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 189,608,636-197,532,175 , GRCh38.p12 chr3: 189,890,847-197,805,304	NCBP2, LINC01972, 174 more genes
nsv6290248	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 191,866,466-197,842,171 , GRCh38.p12 chr3: 192,148,677-198,115,300	NCBP2, PIGZ, 156 more genes
nsv3920444	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 195,540,958-198,905,009 , GRCh38 chr3: 194,338,534-197,693,741 , GRCh37 chr3: 194,059,263-197,420,612	NCBP2, RN7SL36P, 107 more genes
nsv4674423	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 195,652,973-197,346,971 , GRCh38.p12 chr3: 195,926,102-197,620,100	NCBP2, LOC100133326, 54 more genes
nsv6315456	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 195,703,615-197,386,180 , GRCh38.p12 chr3: 195,976,744-197,659,309	NCBP2, PIGX, 54 more genes
nsv7098929	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 195,950,438-197,629,463 , GRCh37.p13 chr3: 195,677,309-197,356,334	NCBP2, LINC01063, 52 more genes
nsv3886526	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 195,690,227-197,356,334 , GRCh38.p12 chr3: 195,963,356-197,629,463	NCBP2, BDH1, 52 more genes
nsv6636887	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 195,690,228-197,356,334 , GRCh38.p12 chr3: 195,963,357-197,629,463	NCBP2, LOC105374307, 52 more genes
nsv3875183	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 195,725,402-197,386,693 , GRCh38.p12 chr3: 195,998,531-197,659,822	NCBP2, TM4SF19-DYNLT2B, 52 more genes
nsv3924895	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 197,185,595-198,845,618 , GRCh37.p13 chr3: 195,701,198-197,361,221 , GRCh38.p12 chr3: 195,974,327-197,634,350	NCBP2, LOC101926923, 53 more genes
nsv3911432	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 197,188,012-198,840,731 , GRCh38 chr3: 195,976,744-197,629,463 , GRCh37 chr3: 195,703,615-197,356,334	NCBP2, LOC101926923, 52 more genes
nsv3872813	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 195,703,615-197,348,575 , GRCh38.p12 chr3: 195,976,744-197,621,704	NCBP2, SDHAP4, 52 more genes
nsv3921980	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 197,166,979-198,809,180 , GRCh37 chr3: 195,682,582-197,324,783 , GRCh38 chr3: 195,955,711-197,597,912	NCBP2, LINC01063, 51 more genes
nsv3879998	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 195,990,063-197,617,301 , GRCh37.p13 chr3: 195,716,934-197,344,172	NCBP2, MIR4797, 52 more genes
nsv3914020	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 195,701,162-197,324,783 , GRCh38 chr3: 195,974,291-197,597,912 , NCBI36 chr3: 197,185,559-198,809,180	NCBP2, FBXO45, 51 more genes
nsv3916750	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 197,247,045-198,869,808 , GRCh38 chr3: 196,035,777-197,658,540 , GRCh37 chr3: 195,762,648-197,385,411	NCBP2, LOC105374308, 52 more genes
nsv3884330	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 195,725,290-197,344,176 , GRCh38.p12 chr3: 195,998,419-197,617,305	NCBP2, RPSAP69, 50 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 103

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Number of Variants: 20

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