borcs6[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
nsv3898050	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,241,916-8,692,213 , GRCh38.p12 chr17: 7,338,597-8,788,895	BORCS6, NDEL1, 108 more genes
nsv7095414	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,123,304-8,193,254 , GRCh38.p12 chr17: 7,219,985-8,289,936	BORCS6, CTC1, 103 more genes
nsv7094915	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,120,455-8,151,423 , GRCh38.p12 chr17: 7,217,136-8,248,105	BORCS6, MIR324, 101 more genes
nsv3923531	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 7,322,238-8,279,567 , GRCh37 chr17: 7,381,514-8,338,842 , GRCh38 chr17: 7,478,195-8,435,524	BORCS6, SLC25A35, 82 more genes
nsv7095365	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,571,752-8,285,628 , GRCh38.p12 chr17: 7,668,434-8,382,310	BORCS6, TRK-TTT3-5, 59 more genes
nsv4453653	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,572,917-8,285,638 , GRCh38 chr17: 7,669,599-8,382,320	BORCS6, TRS-AGA2-6, 59 more genes
nsv3876908	copy number variation	3	nstd102	human	Pathogenic	GRCh37 chr17: 7,572,921-8,285,634 , GRCh38 chr17: 7,669,603-8,382,316	BORCS6, ALOX12B, 59 more genes
nsv6310334	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,571,752-8,135,555 , GRCh38.p12 chr17: 7,668,434-8,232,237	BORCS6, TRAPPC1, 51 more genes
nsv3903684	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004	BORCS6, MIR3185, 2366 more genes
nsv3899740	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564	BORCS6, P4HB, 2366 more genes
nsv3906245	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251	BORCS6, MIR21, 2366 more genes
nsv3907261	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062	BORCS6, SMURF2, 2366 more genes
nsv3897625	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 525-15,027,737 , GRCh38.p12 chr17: 150,732-15,124,420	BORCS6, GP1BA, 439 more genes
nsv3915354	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 150,732-14,764,202 , NCBI36 chr17: 525-14,608,244 , GRCh37 chr17: 525-14,667,519	BORCS6, KIF1C-AS1, 433 more genes
nsv3917059	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 45,835-12,247,218 , NCBI36 chr17: 11,807-12,187,943 , GRCh38 chr17: 162,016-12,343,901	BORCS6, PSMB6, 409 more genes
nsv7148254	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 165,730-11,404,096 , GRCh37.p13 chr17: 396,627-11,307,413	BORCS6, RFLNB, 401 more genes
nsv3904771	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 525-11,186,432 , GRCh38.p12 chr17: 150,732-11,283,115	BORCS6, SLC2A4, 401 more genes
nsv3911050	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 5,732,953-12,095,349 , GRCh37 chr17: 5,636,273-11,998,666 , NCBI36 chr17: 5,576,997-11,939,391	BORCS6, C17orf49, 209 more genes
nsv1398120	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr17: 6,853,665-8,107,394 , GRCh37.p13 chr17: 6,912,941-8,166,669 , GRCh38.p12 chr17: 7,009,622-8,263,351	BORCS6, ACADVL, 117 more genes
nsv3890458	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 8,044,148-8,125,042 , GRCh38.p12 chr17: 8,140,830-8,221,724	BORCS6, TMEM107, 16 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 30

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Number of Variants: 20

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Supplemental Content

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Search details

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