asic4[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
nsv7096611	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 220,299,700-220,357,508 , GRCh38.p12 chr2: 219,434,978-219,492,786	ASIC4-AS1, SPEG
nsv6311201	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 220,355,139-220,355,140 , GRCh38 chr2: 219,490,417-219,490,418	ASIC4-AS1, SPEG
nsv3910630	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331	ASIC4, DAZAP2P1, 2991 more genes
nsv6313668	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 219,606,537-239,217,703 , GRCh38.p12 chr2: 218,741,814-238,309,062	ASIC4, LOC105373947, 357 more genes
nsv3873368	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 218,813,434-227,450,699 , GRCh38.p12 chr2: 217,948,711-226,585,983	ASIC4, ARPC2, 163 more genes
nsv6112757	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 220,056,891-227,164,817 , GRCh38.p12 chr2: 219,192,169-226,300,101	ASIC4, DES, 100 more genes
nsv3906433	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 219,946,342-226,295,024 , GRCh38 chr2: 219,081,620-225,430,308 , NCBI36 chr2: 219,654,586-226,003,268	ASIC4, HIGD1AP4, 102 more genes
nsv3876630	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 219,925,666-220,914,504 , GRCh38.p12 chr2: 219,060,944-220,049,783	ASIC4, ATG9A, 43 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	ASIC4, LOC112268439, 3737 more genes
nsv3874648	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305	ASIC4, IGKV2OR2-10, 3737 more genes
nsv3885544	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609	ASIC4, RNU6-674P, 3735 more genes
nsv3882615	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232	ASIC4, MTND2P22, 3724 more genes
nsv4728725	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306	ASIC4, LOC105376755, 1013 more genes
nsv3890898	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 188,818,195-242,065,208 , NCBI36 chr2: 189,391,166-242,656,032 , GRCh37 chr2: 189,682,921-243,007,359	ASIC4, LOC105373909, 901 more genes
nsv3896499	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 190,300,875-242,783,384 , NCBI36 chr2: 190,009,120-242,432,057 , GRCh38 chr2: 189,436,149-241,841,232	ASIC4, RNU6-1206P, 883 more genes
nsv3908112	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 190,310,736-241,892,770 , NCBI36 chr2: 190,883,707-242,483,594 , GRCh37 chr2: 191,175,462-242,834,921	ASIC4, LOC101928084, 871 more genes
nsv3902143	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 180,513,793-224,302,848 , NCBI36 chr2: 181,086,765-224,875,809 , GRCh37 chr2: 181,378,520-225,167,565	ASIC4, LINC00607, 644 more genes
nsv3892046	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 195,763,507-237,382,556 , NCBI36 chr2: 195,471,752-237,047,295 , GRCh38 chr2: 194,898,783-236,473,913	ASIC4, NPM1P46, 706 more genes
nsv7148056	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 186,698,504-223,918,111 , GRCh38.p12 chr2: 185,833,777-223,053,393	ASIC4, DNAJB1P1, 580 more genes
nsv4436532	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 188,926,928-225,298,653 , GRCh38.p12 chr2: 188,062,201-224,433,936	ASIC4, MARS2, 575 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 34

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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