ptk6[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
nsv7096084	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 62,119,651-62,159,505 , GRCh38.p12 chr20: 63,488,298-63,528,152	PTK6, EEF1A2, 3 more genes
nsv4683374	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 62,124,470-62,159,505 , GRCh38.p12 chr20: 63,493,117-63,528,152	PTK6, LOC102723814, 3 more genes
nsv4682468	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 62,037,977-62,159,505 , GRCh38.p12 chr20: 63,406,624-63,528,152	PTK6, EEF1A2, 7 more genes
nsv3882621	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 62,075,992-62,159,505 , GRCh38 chr20: 63,444,639-63,528,152	PTK6, EEF1A2, 5 more genes
nsv4450139	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 62,103,501-62,159,505 , GRCh38 chr20: 63,472,148-63,528,152	PTK6, EEF1A2, 4 more genes
nsv6314131	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,003,263-62,915,555 , GRCh38.p12 chr20: 62,428,207-64,284,202	PTK6, HAR1A, 100 more genes
nsv4676208	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,152,321-62,915,555 , GRCh38.p12 chr20: 62,555,114-64,284,202	PTK6, GMEB2, 94 more genes
nsv3916163	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,211,869-62,908,674 , GRCh38 chr20: 62,561,794-64,277,321 , NCBI36 chr20: 60,569,446-62,379,118	PTK6, LOC105372727, 94 more genes
nsv3916631	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,179,280-62,915,555 , NCBI36 chr20: 60,589,725-62,385,999 , GRCh38 chr20: 62,582,073-64,284,202	PTK6, LOC105372719, 91 more genes
nsv3922590	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 60,553,022-62,343,283 , GRCh38 chr20: 62,545,370-64,241,486 , GRCh37 chr20: 61,142,577-62,872,839	PTK6, RPL7P3, 95 more genes
nsv3913089	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 60,765,104-62,385,999 , GRCh37 chr20: 61,294,659-62,915,555 , GRCh38 chr20: 62,663,307-64,284,202	PTK6, SLCO4A1-AS1, 89 more genes
nsv3922908	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 61,010,752-62,435,964 , GRCh37.p13 chr20: 61,540,307-62,965,520 , GRCh38.p12 chr20: 62,908,955-64,334,167	PTK6, NPBWR2, 78 more genes
nsv3911578	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 62,455,231-63,839,491 , NCBI36 chr20: 60,463,682-61,941,288 , GRCh37 chr20: 61,030,287-62,470,844	PTK6, LOC105372716, 70 more genes
nsv6314091	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,619,222-62,915,555 , GRCh38.p12 chr20: 62,987,870-64,284,202	PTK6, TPD52L2, 72 more genes
nsv7148178	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 62,632,017-63,794,804 , GRCh37.p13 chr20: 61,267,734-62,426,157	PTK6, GID8, 60 more genes
nsv6291738	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,775,756-62,915,555 , GRCh38.p12 chr20: 63,144,404-64,284,202	PTK6, C20orf204, 63 more genes
nsv3911666	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,785,315-62,908,674 , GRCh38 chr20: 63,153,963-64,277,321 , NCBI36 chr20: 61,255,760-62,379,118	PTK6, MIR3196, 63 more genes
nsv3900085	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,827,144-62,907,526 , GRCh38.p12 chr20: 63,195,792-64,276,173	PTK6, PCMTD2, 62 more genes
nsv3909648	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,827,144-62,907,467 , GRCh38.p12 chr20: 63,195,792-64,276,114	PTK6, LOC100130587, 62 more genes
nsv3909335	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,884,113-62,915,555 , GRCh38.p12 chr20: 63,252,761-64,284,202	PTK6, TCEA2, 59 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 87

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Number of Variants: 20

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Supplemental Content

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Search details

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