rprd1a[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
nsv1398386	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr18: 33,611,007-33,722,860 , GRCh38.p12 chr18: 36,031,044-36,142,897	RPRD1A, ELP2, 1 more genes
nsv6314722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 1,262,334-53,254,751 , GRCh38.p12 chr18: 1,262,333-55,587,520	RPRD1A, LOC107985176, 632 more genes
nsv3900710	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 20,069,932-36,887,326 , GRCh38.p12 chr18: 22,489,969-39,307,362	RPRD1A, CABLES1, 174 more genes
nsv3912224	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 27,945,491-39,904,182 , GRCh38 chr18: 32,111,530-44,070,219 , GRCh37 chr18: 29,691,493-41,650,184	RPRD1A, SYT4, 94 more genes
nsv4676233	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 22,868,759-34,335,753 , GRCh38.p12 chr18: 25,288,795-36,755,790	RPRD1A, DHFRP1, 116 more genes
nsv3912888	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 27,024,475-37,983,616 , NCBI36 chr18: 25,278,473-36,237,614 , GRCh38 chr18: 29,444,510-40,403,652	RPRD1A, KLHL14, 107 more genes
nsv4729854	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 23,971,647-33,737,300 , GRCh38.p12 chr18: 26,391,683-36,157,337	RPRD1A, CLUHP6, 100 more genes
nsv3920302	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 29,881,080-37,228,316 , GRCh38 chr18: 34,047,118-41,394,354 , GRCh37 chr18: 31,627,082-38,974,318	RPRD1A, FHOD3, 61 more genes
nsv3897721	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 29,711,972-35,866,193 , GRCh38.p12 chr18: 32,132,009-38,286,229	RPRD1A, LOC105372073, 56 more genes
nsv4350805	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 33,554,981-36,939,357 , GRCh38.p12 chr18: 35,975,018-39,359,393	RPRD1A, LOC101927879, 28 more genes
nsv6315530	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271	RPRD1A, LOC105372145, 947 more genes
nsv3907444	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 12,842-78,015,180 , GRCh38.p12 chr18: 12,842-80,257,297	RPRD1A, GALNT1, 947 more genes
nsv3890669	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 13,034-78,015,180 , GRCh38.p12 chr18: 13,034-80,257,297	RPRD1A, MYL12B, 947 more genes
nsv3918488	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 43,345-76,068,860 , GRCh38 chr18: 53,345-80,209,986 , GRCh37 chr18: 53,345-77,967,869	RPRD1A, LOC105372027, 945 more genes
nsv3924351	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 108,760-76,113,817 , GRCh38 chr18: 118,760-80,254,946 , GRCh37 chr18: 118,760-78,012,829	RPRD1A, MIX23P1, 942 more genes
nsv3919004	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr18: 136,226-80,256,240 , GRCh37 chr18: 136,226-78,014,123 , NCBI36 chr18: 126,226-76,115,097	RPRD1A, LIVAR, 941 more genes
nsv3899451	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 136,226-78,014,123 , GRCh38.p12 chr18: 136,226-80,256,240	RPRD1A, BOLA2P1, 941 more genes
nsv3924706	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 136,227-78,014,123 , GRCh38 chr18: 136,227-80,256,240 , NCBI36 chr18: 126,227-76,115,097	RPRD1A, LOC100420948, 941 more genes
nsv3907722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 136,227-78,014,123 , GRCh38.p12 chr18: 136,227-80,256,240	RPRD1A, ROCK1, 941 more genes
nsv3910887	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 139,089-76,113,807 , GRCh37 chr18: 149,089-78,012,819 , GRCh38 chr18: 149,089-80,254,936	RPRD1A, LPIN2, 941 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 49

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Number of Variants: 20

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