ush1c[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
nsv5672627	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 17,526,184-17,548,597 , GRCh38.p12 chr11: 17,504,637-17,527,050	USH1C
nsv6308966	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 17,548,750-17,565,854 , GRCh38.p12 chr11: 17,527,203-17,544,307	USH1C
nsv6309105	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 17,552,691-17,565,973 , GRCh38.p12 chr11: 17,531,144-17,544,426	USH1C
nsv7093677	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 17,522,588-17,527,506 , GRCh38.p12 chr11: 17,501,041-17,505,959	USH1C
nsv5672626	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 17,522,578-17,523,547 , GRCh38.p12 chr11: 17,501,031-17,502,000	USH1C
nsv6308967	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 17,552,681-17,552,859 , GRCh38.p12 chr11: 17,531,134-17,531,312	USH1C
nsv7093676	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 17,519,689-17,523,547 , GRCh38.p12 chr11: 17,498,142-17,502,000	USH1C
nsv6309103	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 17,474,656-17,542,968 , GRCh38.p12 chr11: 17,453,109-17,521,421	USH1C, ABCC8
nsv4456076	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 17,468,457-17,543,203 , GRCh38.p12 chr11: 17,446,910-17,521,656	USH1C, ABCC8
nsv4682515	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 17,555,235-17,667,491 , GRCh38.p12 chr11: 17,533,688-17,645,944	USH1C, OTOG
nsv6309039	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 17,448,576-17,600,093 , GRCh38.p12 chr11: 17,427,029-17,578,546	USH1C, ABCC8, 2 more genes
nsv5380796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397	USH1C, FAUP4, 2031 more genes
nsv3893233	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576	USH1C, LOC105376598, 2842 more genes
nsv3900144	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169	USH1C, RTN3, 2833 more genes
nsv3908873	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576	USH1C, IGHMBP2, 2829 more genes
nsv3898926	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-37,698,540 , GRCh38.p12 chr11: 230,615-37,676,990	USH1C, OR51L1, 771 more genes
nsv4674879	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449	USH1C, BGLT3, 723 more genes
nsv3906221	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-31,995,219 , GRCh38.p12 chr11: 230,615-31,973,673	USH1C, PCNAP4, 688 more genes
nsv6315535	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599	USH1C, OR52Q1P, 630 more genes
nsv3894525	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-25,584,362 , GRCh38.p12 chr11: 230,615-25,562,816	USH1C, SDHCP4, 620 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 31

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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