prdm12[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
nsv4768342	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 130,677,172-130,686,904 , GRCh37 chr9: 133,552,559-133,562,291	PRDM12
nsv4685725	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 133,553,916-133,554,028 , GRCh38.p12 chr9: 130,678,529-130,678,641	PRDM12
nsv6313257	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr9: 133,553,896-133,557,056 , GRCh38.p12 chr9: 130,678,509-130,681,669	PRDM12
nsv3885319	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 133,553,896-133,554,047 , GRCh38 chr9: 130,678,509-130,678,660	PRDM12
nsv4683914	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 133,540,031-133,557,066 , GRCh38.p12 chr9: 130,664,644-130,681,679	PRDM12
nsv6313256	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 133,540,041-133,543,720 , GRCh38.p12 chr9: 130,664,654-130,668,333	PRDM12
nsv3899776	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 129,370,440-133,866,894 , GRCh38.p12 chr9: 126,608,161-130,991,507	PRDM12, FNBP1, 136 more genes
nsv3911736	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 132,712,094-135,217,877 , NCBI36 chr9: 131,751,915-134,207,698 , GRCh38 chr9: 129,949,815-132,342,490	PRDM12, HMCN2, 40 more genes
nsv3912247	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 2,934-140,273,252 , GRCh37.p13 chr9: 12,934-141,153,431 , GRCh38.p12 chr9: 12,934-138,262,981	PRDM12, ALOX15P2, 2184 more genes
nsv3890420	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,122,247 , GRCh38.p12 chr9: 10,590-138,231,797	PRDM12, TBC1D13, 2183 more genes
nsv3905118	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,114,095 , GRCh38.p12 chr9: 10,590-138,223,645	PRDM12, MIR219A2, 2183 more genes
nsv3891842	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,107,672 , GRCh38.p12 chr9: 10,590-138,217,222	PRDM12, OR13C1P, 2183 more genes
nsv3895453	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 46,587-141,066,491 , GRCh38.p12 chr9: 46,587-138,172,039	PRDM12, RPL19P15, 2176 more genes
nsv3900967	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 163,131-141,122,114 , GRCh38.p12 chr9: 163,131-138,231,664	PRDM12, BANCR, 2173 more genes
nsv3907479	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 62,525-141,006,407 , GRCh38.p12 chr9: 62,525-138,111,955	PRDM12, OR2AM1P, 2174 more genes
nsv3922684	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897	PRDM12, TDRD7, 2170 more genes
nsv3919257	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 204,193-141,073,897 , GRCh38 chr9: 204,193-138,179,445 , NCBI36 chr9: 194,193-140,193,718	PRDM12, LOC107987031, 2169 more genes
nsv3915973	copy number variation	2	nstd102	human	Pathogenic	GRCh38 chr9: 193,412-138,159,073 , GRCh37 chr9: 68,420,641-141,053,525 , NCBI36 chr9: 67,910,461-140,173,346	PRDM12, CTNNAL1, 2170 more genes
nsv3911025	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 193,412-138,124,524 , NCBI36 chr9: 194,090-140,138,797 , GRCh37 chr9: 204,090-141,018,976	PRDM12, RORB-AS1, 2168 more genes
nsv3921598	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 203,861-138,125,937 , NCBI36 chr9: 193,861-140,140,210 , GRCh37 chr9: 203,861-141,020,389	PRDM12, PGAP4, 2167 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 44

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Number of Variants: 20

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