pdlim7[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
nsv1398443	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 174,397,487-180,686,444 , GRCh38.p12 chr5: 174,970,484-181,259,443	PDLIM7, TRV-AAC1-3, 203 more genes
nsv3920109	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 174,896,380-180,652,395 , GRCh37 chr5: 174,963,774-180,719,789 , GRCh38 chr5: 175,536,771-181,292,788	PDLIM7, LOC100289470, 198 more genes
nsv3873295	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 175,570,677-180,719,789 , GRCh38.p12 chr5: 176,143,674-181,292,788	PDLIM7, LINC02222, 186 more genes
nsv3922812	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 176,059,735-180,629,412 , GRCh38 chr5: 176,700,128-181,269,805 , GRCh37 chr5: 176,127,129-180,696,806	PDLIM7, MRPL50P3, 167 more genes
nsv3913935	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 176,291,838-178,662,699 , NCBI36 chr5: 175,651,447-178,022,306 , GRCh37 chr5: 175,718,841-178,089,700	PDLIM7, DBN1, 74 more genes
nsv3883303	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 176,918,345-179,061,393 , GRCh38.p12 chr5: 177,491,344-179,634,392	PDLIM7, GMCL2, 60 more genes
nsv4685982	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 175,346,695-177,469,711 , GRCh38.p12 chr5: 175,919,692-178,042,710	PDLIM7, NOP16, 65 more genes
nsv3880232	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 175,346,223-177,423,236 , GRCh38.p12 chr5: 175,919,220-177,996,235	PDLIM7, MIR4281, 63 more genes
nsv3882029	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 175,438,045-177,481,250 , GRCh38.p12 chr5: 176,011,042-178,054,249	PDLIM7, LOC105377752, 64 more genes
nsv3917273	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 175,989,092-178,009,412 , NCBI36 chr5: 175,348,701-177,369,019 , GRCh37 chr5: 175,416,095-177,436,413	PDLIM7, LOC105377752, 64 more genes
nsv3875513	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 175,433,876-177,441,189 , GRCh38.p12 chr5: 176,006,873-178,014,188	PDLIM7, RAB24, 64 more genes
nsv3880220	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 175,438,045-177,392,885 , GRCh38.p12 chr5: 176,011,042-177,965,884	PDLIM7, MIR4281, 59 more genes
nsv3909885	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 175,403,085-177,355,366 , GRCh38 chr5: 176,043,476-177,995,759 , GRCh37 chr5: 175,470,479-177,422,760	PDLIM7, SNCB, 60 more genes
nsv3888764	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 175,492,445-177,359,136 , GRCh37.p13 chr5: 175,559,839-177,426,530 , GRCh38.p12 chr5: 176,132,836-177,999,529	PDLIM7, ARL10, 57 more genes
nsv3889409	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 175,570,678-177,437,340 , GRCh38.p12 chr5: 176,143,675-178,010,339	PDLIM7, MIR4281, 59 more genes
nsv3924491	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 175,570,677-177,436,413 , GRCh38 chr5: 176,143,674-178,009,412 , NCBI36 chr5: 175,503,283-177,369,019	PDLIM7, CDHR2, 59 more genes
nsv3883776	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 175,570,677-177,436,413 , GRCh38.p12 chr5: 176,143,674-178,009,412	PDLIM7, MIR1271, 59 more genes
nsv3914974	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 176,132,340-177,995,759 , NCBI36 chr5: 175,491,949-177,355,366 , GRCh37 chr5: 175,559,343-177,422,760	PDLIM7, RN7SL684P, 57 more genes
nsv3910181	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 175,511,682-177,345,820 , GRCh37 chr5: 175,579,076-177,413,214 , GRCh38 chr5: 176,152,073-177,986,213	PDLIM7, DBN1, 56 more genes
nsv3916122	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 175,474,866-177,006,240 , GRCh38 chr5: 176,115,257-177,646,633 , GRCh37 chr5: 175,542,260-177,073,634	PDLIM7, B4GALT7, 49 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 68

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 68

Page of 4

Number of Variants: 20

Page of 4

Supplemental Content

Find related data

Search details

Recent activity