dnajb13[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 19

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Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3874374	copy number variation	1	nstd102	human	not provided	GRCh37 chr11: 73,638,858-73,708,521 , GRCh38 chr11: 73,927,813-73,997,476	DNAJB13, LOC100421622, 3 more genes
esv3648573	copy number variation	1	estd216	human	not provided	GRCh37 chr11: 73,638,858-73,708,521 , GRCh38.p12 chr11: 73,927,813-73,997,476	DNAJB13, UCP2, 3 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	DNAJB13, FAUP4, 2031 more genes
nsv3915804	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 71,680,927-77,943,941 , NCBI36 chr11: 71,358,575-77,621,589 , GRCh38 chr11: 71,969,881-78,232,895	DNAJB13, TPBGL, 173 more genes
nsv3916301	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 71,928,796-77,064,521 , GRCh37 chr11: 71,639,842-76,751,808 , NCBI36 chr11: 71,317,490-76,453,216	DNAJB13, RN7SL786P, 146 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	DNAJB13, 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	DNAJB13, 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	DNAJB13, IGHMBP2, 2829 more genes
nsv6315537	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576	DNAJB13, PYGM, 2125 more genes
nsv3898361	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 71,588,805-116,680,918 , GRCh38.p12 chr11: 71,877,759-116,810,202	DNAJB13, SESN3, 694 more genes
nsv3900482	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr11: 73,570,217-73,687,662 , GRCh38.p12 chr11: 73,859,172-73,976,617	DNAJB13, COA4, 4 more genes
nsv3917175	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr11: 73,247,865-73,365,853 , GRCh37 chr11: 73,570,217-73,688,205 , GRCh38 chr11: 73,859,172-73,977,160	DNAJB13, COA4, 4 more genes
nsv7094183	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 71,146,421-75,283,128 , GRCh38.p12 chr11: 71,435,375-75,572,083	DNAJB13, LOC112268078, 142 more genes
nsv4455639	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 73,128,157-73,788,461 , GRCh38.p12 chr11: 73,417,112-74,077,416	DNAJB13, RAB6A, 16 more genes
nsv3920330	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr11: 72,963,618-73,522,072 , GRCh38 chr11: 73,574,925-74,133,379 , GRCh37 chr11: 73,285,970-73,844,424	DNAJB13, UCP3, 16 more genes
nsv3891953	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 73,254,213-73,770,541 , GRCh38.p12 chr11: 73,543,168-74,059,496	DNAJB13, DPPA4P3, 16 more genes
nsv3890585	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 73,197,127-73,712,308 , GRCh38.p12 chr11: 73,486,082-74,001,263	DNAJB13, LOC100419713, 15 more genes
nsv4456614	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 73,395,712-73,788,461 , GRCh38.p12 chr11: 73,684,667-74,077,416	DNAJB13, PAAF1, 12 more genes
nsv3907532	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 73,444,963-73,777,547 , GRCh38.p12 chr11: 73,733,918-74,066,502	DNAJB13, UCP2, 11 more genes

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dnajb13[All Fields] AND 1[has_clinical] (21)
dbVar
55230[Gene ID] (140)
ClinVar

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