dnajb6[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
nsv3900588	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 157,128,267-157,252,849 , GRCh38.p12 chr7: 157,335,573-157,460,155	DNAJB6
nsv6312336	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 157,151,257-157,208,802 , GRCh38.p12 chr7: 157,358,563-157,416,108	DNAJB6
nsv6312338	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 157,151,267-157,208,792 , GRCh38.p12 chr7: 157,358,573-157,416,098	DNAJB6
nsv7097878	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 157,177,541-157,208,792 , GRCh38.p12 chr7: 157,384,847-157,416,098	DNAJB6
nsv6312337	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 157,151,267-157,160,197 , GRCh38.p12 chr7: 157,358,573-157,367,503	DNAJB6
nsv7097357	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 157,202,469-157,208,792 , GRCh38.p12 chr7: 157,409,775-157,416,098	DNAJB6
nsv6312623	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 157,208,690-157,208,792 , GRCh38.p12 chr7: 157,415,996-157,416,098	DNAJB6
nsv4455918	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 157,134,943-157,287,531 , GRCh38.p12 chr7: 157,342,249-157,494,837	DNAJB6, LOC101927914
nsv4456670	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 157,060,274-157,166,765 , GRCh38.p12 chr7: 157,267,580-157,374,071	DNAJB6, UBE3C
nsv3910673	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr7: 156,887,264-157,059,432 , GRCh37.p13 chr7: 157,194,503-157,366,671 , GRCh38.p12 chr7: 157,401,809-157,573,979	DNAJB6, LOC101927914, 3 more genes
nsv3919826	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840	DNAJB6, RNU6-438P, 2682 more genes
nsv4675615	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 131,414,604-159,126,310 , GRCh38.p12 chr7: 131,729,845-159,333,620	DNAJB6, ATG9B, 603 more genes
nsv3915633	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 134,002,121-158,077,335 , GRCh38 chr7: 134,666,829-158,591,882 , GRCh37 chr7: 134,351,581-158,384,574	DNAJB6, MOXD2P, 561 more genes
nsv3897512	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 137,917,376-159,119,707 , GRCh38.p12 chr7: 138,232,630-159,327,017	DNAJB6, LOC105375548, 520 more genes
nsv3903590	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 140,133,025-158,982,771 , GRCh38.p12 chr7: 140,433,225-159,190,080	DNAJB6, LOC105375597, 468 more genes
nsv3910344	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 140,754,198-159,307,523 , GRCh37 chr7: 140,453,998-159,100,212 , NCBI36 chr7: 140,100,467-158,792,973	DNAJB6, LOC112268012, 461 more genes
nsv3905379	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 140,636,858-159,119,707 , GRCh38.p12 chr7: 140,937,058-159,327,017	DNAJB6, AGAP3, 459 more genes
nsv3919772	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 141,307,130-158,821,317 , GRCh37 chr7: 142,528,609-159,128,556 , GRCh38 chr7: 141,960,861-159,335,866	DNAJB6, LOC105375567, 429 more genes
nsv3904188	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 141,938,235-159,126,310 , GRCh38.p12 chr7: 142,288,582-159,333,620	DNAJB6, RBM33-DT, 423 more genes
nsv3915683	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 143,884,559-159,282,390 , GRCh37 chr7: 143,581,652-159,075,079 , NCBI36 chr7: 143,212,585-158,767,840	DNAJB6, FASTK, 280 more genes

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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 100

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Number of Variants: 20

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