amy2b[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
nsv4674219	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr1: 103,767,538-104,132,185 , GRCh38.p12 chr1: 103,301,981-103,589,563	AMY2B, ACTG1P4, 3 more genes
nsv6290430	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr1: 103,772,743-104,132,185 , GRCh38.p12 chr1: 103,307,184-103,589,563	AMY2B, RNPC3-DT, 3 more genes
nsv3886464	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 103,916,755-104,136,650 , GRCh38.p12 chr1: 103,374,133-103,594,028	AMY2B, RN7SKP285, 3 more genes
nsv3894916	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr1: 103,777,493-103,956,813 , GRCh38 chr1: 103,462,283-103,612,668 , GRCh37 chr1: 104,004,905-104,155,290	AMY2B, ACTG1P4, 3 more genes
nsv3892934	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 104,107,559-104,163,781 , NCBI36 chr1: 103,909,082-103,965,304 , GRCh38 chr1: 103,564,937-103,621,159	AMY2B, AMY2A, 1 more genes
nsv3902638	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 103,573,857-104,107,589 , NCBI36 chr1: 103,346,445-103,909,112 , GRCh38 chr1: 103,108,301-103,564,967	AMY2B, RNPC3, 3 more genes
nsv6313675	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 95,046,805-114,714,931 , GRCh38.p12 chr1: 94,581,249-114,172,309	AMY2B, LINC01307, 320 more genes
nsv5381058	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 102,021,465-119,737,478 , GRCh38.p12 chr1: 101,555,909-119,194,855	AMY2B, AMYP1, 320 more genes
nsv3893941	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 97,648,746-111,014,655 , GRCh37 chr1: 97,876,158-111,213,132 , GRCh38 chr1: 97,410,602-110,670,510	AMY2B, RPSAP19, 196 more genes
nsv3909776	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 97,737,905-109,435,760 , GRCh38 chr1: 97,272,349-108,893,138 , NCBI36 chr1: 97,510,493-109,237,283	AMY2B, SNX7, 133 more genes
nsv3901500	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 101,856,241-112,047,173 , GRCh38 chr1: 101,618,097-111,703,028 , GRCh37 chr1: 102,083,653-112,245,650	AMY2B, CHIAP1, 171 more genes
nsv3920130	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 103,429,843-112,252,782 , GRCh37.p13 chr1: 103,657,255-112,451,259 , GRCh38.p12 chr1: 103,191,699-111,908,637	AMY2B, LOC105378898, 166 more genes
nsv3916187	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 97,510,536-104,123,269 , GRCh37.p13 chr1: 97,737,948-104,321,746 , GRCh38.p12 chr1: 97,272,392-103,779,124	AMY2B, SLC35A3, 80 more genes
nsv4674238	copy number variation	1	nstd102	human	Pathogenic	GRCh38.p12 chr1: 103,067,148-103,589,563 , GRCh37 chr1: 103,532,704-104,132,185	AMY2B, COL11A1, 5 more genes
nsv3877365	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250	AMY2B, MARK1, 4930 more genes
nsv3885206	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793	AMY2B, SNAP47, 4927 more genes
nsv3884414	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485	AMY2B, RNU1-153P, 4887 more genes
nsv3882464	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 93,837,992-121,343,783 , GRCh38.p12 chr1: 93,372,435-121,601,985	AMY2B, LINC02607, 513 more genes
nsv3898327	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 83,457,325-104,273,917 , GRCh37 chr1: 83,923,008-104,816,539 , NCBI36 chr1: 83,695,596-104,618,062	AMY2B, LINC01773, 322 more genes
nsv3884558	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 94,054,724-111,671,707 , GRCh38.p12 chr1: 93,589,167-111,129,085	AMY2B, SLC25A24, 265 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 43

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Number of Variants: 20

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Supplemental Content

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Search details

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