ppid[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
nsv7096838	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 159,593,534-159,629,689 , GRCh38.p12 chr4: 158,672,382-158,708,537	PPID, C4orf46, 1 more genes
nsv3912510	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr4: 159,834,270-160,132,396 , GRCh37.p13 chr4: 159,614,820-159,912,946 , GRCh38.p12 chr4: 158,693,668-158,991,794	PPID, ETFDH, 3 more genes
nsv5059966	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr4: 158,620,034-158,710,227 , GRCh37 chr4: 159,541,186-159,631,379	PPID, RXFP1, 2 more genes
nsv6311910	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 159,593,609-159,629,679 , GRCh38.p12 chr4: 158,672,457-158,708,527	PPID, C4orf46, 1 more genes
nsv6634351	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 159,174,483-190,957,473 , GRCh38.p12 chr4: 158,253,331-190,036,318	PPID, COPS3P1, 363 more genes
nsv3919458	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 155,162,982-170,959,553 , GRCh37 chr4: 156,084,134-171,880,704 , NCBI36 chr4: 156,303,584-172,117,279	PPID, AIDAP2, 172 more genes
nsv5381776	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 157,771,352-172,496,278 , GRCh38.p12 chr4: 156,850,200-171,575,127	PPID, LOC107986326, 144 more genes
nsv3874224	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 153,203,431-162,912,359 , GRCh38.p12 chr4: 152,282,279-161,991,207	PPID, PLRG1, 120 more genes
nsv3873978	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 11,525-191,028,879 , GRCh38.p12 chr4: 11,525-190,107,724	PPID, LOC100422029, 2358 more genes
nsv3876533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-190,963,766 , GRCh38.p12 chr4: 49,556-190,042,611	PPID, LOC100420289, 2347 more genes
nsv3884499	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 12,440-190,904,441 , GRCh38.p12 chr4: 12,440-189,983,286	PPID, MTND4LP29, 2341 more genes
nsv3880085	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr4: 68,346-190,957,473 , GRCh38.p12 chr4: 68,454-190,036,318	PPID, LOC112268460, 2345 more genes
nsv3883791	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-190,915,650 , GRCh38.p12 chr4: 49,556-189,994,495	PPID, LOC105377343, 2341 more genes
nsv3875534	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 93,071,152-190,957,473 , GRCh38.p12 chr4: 92,150,001-190,036,318	PPID, KLKB1, 1118 more genes
nsv3874596	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 109,199,664-189,752,726 , GRCh38.p12 chr4: 108,278,508-188,831,572	PPID, RPL6P12, 938 more genes
nsv3924008	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 118,065,569-190,042,639 , GRCh37 chr4: 118,986,724-190,828,225 , NCBI36 chr4: 119,206,172-191,200,788	PPID, METTL14-DT, 828 more genes
nsv3874610	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 119,437,495-190,904,301 , GRCh38.p12 chr4: 118,516,340-189,983,146	PPID, OTUD4, 813 more genes
nsv3918110	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 122,658,828-191,220,419 , GRCh38 chr4: 121,518,223-190,062,270 , GRCh37 chr4: 122,439,378-190,828,225	PPID, SCRG1, 770 more genes
nsv4455301	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 124,873,497-185,278,662 , GRCh38.p12 chr4: 123,952,342-184,357,509	PPID, SMARCA5, 633 more genes
nsv3911855	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 125,432,943-185,761,887 , GRCh37 chr4: 126,354,098-186,683,041 , NCBI36 chr4: 126,573,548-186,920,035	PPID, RPL26P16, 656 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 42

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Number of Variants: 20

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Supplemental Content

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