prr7[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
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	PRR7, 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	PRR7, 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	PRR7, 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	PRR7, 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	PRR7, DBN1, 74 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	PRR7, 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	PRR7, 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	PRR7, 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	PRR7, 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	PRR7, 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	PRR7, 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	PRR7, 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	PRR7, 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	PRR7, 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	PRR7, 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	PRR7, 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	PRR7, 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	PRR7, 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	PRR7, B4GALT7, 49 more genes
nsv3915945	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 175,579,076-177,073,634 , NCBI36 chr5: 175,511,682-177,006,240 , GRCh38 chr5: 176,152,073-177,646,633	PRR7, ARL10, 47 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 68

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Number of Variants: 20

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Search details

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