pnldc1[All Fields] AND 1[has_clinical] - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3911475	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 152,793,402-170,610,394 , GRCh37 chr6: 153,114,537-170,919,482 , NCBI36 chr6: 153,156,230-170,761,407	PNLDC1, SNORA116, 275 more genes
nsv3913213	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 154,118,058-170,602,152 , NCBI36 chr6: 154,480,885-170,753,165 , GRCh37 chr6: 154,439,193-170,911,240	PNLDC1, LDHAL6FP, 258 more genes
nsv3921695	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 154,539,655-170,714,507 , NCBI36 chr6: 154,902,481-170,865,520 , GRCh37 chr6: 154,860,789-171,023,595	PNLDC1, LOC105378128, 255 more genes
nsv6315428	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 159,121,459-170,919,482 , GRCh38.p12 chr6: 158,700,427-170,610,394	PNLDC1, TBP, 200 more genes
nsv3921491	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 159,795,661-170,763,014 , GRCh38 chr6: 159,454,639-170,612,001 , GRCh37 chr6: 159,875,671-170,921,089	PNLDC1, LOC102724357, 183 more genes
nsv1397956	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 159,830,469-170,673,013 , GRCh37.p13 chr6: 159,910,479-170,831,088 , GRCh38.p12 chr6: 159,489,447-170,522,000	PNLDC1, LOC107986675, 179 more genes
nsv6313530	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 153,207,930-164,322,346 , GRCh38.p12 chr6: 152,886,795-163,901,314	PNLDC1, RSPH3, 144 more genes
nsv6634356	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 157,318,401-165,233,548 , GRCh38.p12 chr6: 156,997,267-164,820,059	PNLDC1, LOC105378097, 103 more genes
nsv3916251	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 155,378,049-163,133,499 , NCBI36 chr6: 155,740,875-163,474,521 , GRCh37 chr6: 155,699,183-163,554,531	PNLDC1, MAP3K4, 99 more genes
nsv7097050	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 158,532,398-162,868,359 , GRCh38.p12 chr6: 158,111,366-162,447,327	PNLDC1, LOC107986665, 64 more genes
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	PNLDC1, LOC105378061, 2914 more genes
nsv3879811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083	PNLDC1, RNU6-411P, 2910 more genes
nsv3887898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394	PNLDC1, SOD1P1, 2905 more genes
nsv3889814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382	PNLDC1, ITPR3, 2905 more genes
nsv3911993	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 133,900,102-166,209,023 , GRCh38 chr6: 133,537,271-165,875,545 , GRCh37 chr6: 133,858,409-166,289,033	PNLDC1, LOC105369171, 418 more genes
nsv3920975	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 141,454,127-169,739,666 , GRCh38 chr6: 141,132,990-169,339,571 , NCBI36 chr6: 141,495,820-169,481,591	PNLDC1, UST-AS2, 394 more genes
nsv3908622	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 150,284,435-170,919,470 , GRCh38.p12 chr6: 149,963,299-170,610,382	PNLDC1, LOC105378120, 319 more genes
nsv3904213	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 151,214,792-170,892,243 , GRCh38.p12 chr6: 150,893,656-170,583,155	PNLDC1, CTAGE13P, 304 more genes
nsv3913037	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 152,697,473-170,921,089 , GRCh38 chr6: 152,376,338-170,612,001 , NCBI36 chr6: 152,739,166-170,763,014	PNLDC1, KRT8P44, 283 more genes
nsv3909469	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 159,155,998-171,054,786 , GRCh38.p12 chr6: 158,734,966-170,745,698	PNLDC1, LOC101929614, 203 more genes

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

Send to:

Search results

Items: 1 to 20 of 27

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Search details

Recent activity

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 27

Page of 2

Number of Variants: 20

Page of 2

Supplemental Content

Find related data

Search details

Recent activity