dph5[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 14

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Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
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	DPH5, LINC01307, 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	DPH5, 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	DPH5, SNX7, 133 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	DPH5, SLC35A3, 80 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	DPH5, 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	DPH5, 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	DPH5, 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	DPH5, 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	DPH5, 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	DPH5, SLC25A24, 265 more genes
nsv6290366	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 100,215,607-105,368,230 , GRCh38.p12 chr1: 99,750,051-104,825,608	DPH5, LOC105379827, 63 more genes
nsv5060026	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 101,326,711-104,423,819 , GRCh38.p12 chr1: 100,861,155-103,881,197	DPH5, LOC105378878, 33 more genes
nsv4436181	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532	DPH5, LINC01776, 1853 more genes
nsv7095681	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 100,316,599-101,709,564 , GRCh38.p12 chr1: 99,851,043-101,244,008	DPH5, SLC35A3, 29 more genes

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