dbVar for Gene (Select 4602) - 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
nsv7056994	inversion	1	nstd229	human		GRCh38 chr6: 135,215,451-135,215,499 , GRCh37.p13 chr6: 135,536,589-135,536,637	LOC105378011, MYB
nsv6814996	copy number variation	1	nstd229	human		GRCh38 chr6: 135,074,201-135,333,400 , GRCh37.p13 chr6: 135,395,339-135,654,538	MIR548A2, AHI1, 4 more genes
nsv6807331	copy number variation	1	nstd229	human		GRCh38 chr6: 134,409,841-135,998,734 , GRCh37.p13 chr6: 134,730,979-136,319,872	MYB, LINC01010, 21 more genes
nsv6611528	copy number variation	1	nstd223	human		GRCh38 chr6: 135,180,201-135,184,100 , GRCh37.p13 chr6: 135,501,339-135,505,238	MYB
nsv6607168	copy number variation	1	nstd223	human		GRCh38 chr6: 135,180,701-135,182,200 , GRCh37.p13 chr6: 135,501,839-135,503,338	MYB
nsv6600592	copy number variation	1	nstd223	human		GRCh38 chr6: 135,180,701-135,183,900 , GRCh37.p13 chr6: 135,501,839-135,505,038	MYB
nsv6570037	inversion	1	nstd223	human		GRCh38 chr6: 135,204,555-135,204,692 , GRCh37.p13 chr6: 135,525,693-135,525,830	MYB, LOC105378011
nsv6563419	inversion	1	nstd223	human		GRCh38 chr6: 134,890,896-135,471,959 , GRCh37.p13 chr6: 135,212,034-135,793,097	MIR548A2, MIR3662, 8 more genes
nsv6557020	inversion	1	nstd223	human		GRCh38 chr6: 135,206,058-135,208,541 , GRCh37.p13 chr6: 135,527,196-135,529,679	MYB, LOC105378011
nsv6314818	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 134,838,331-142,160,056 , GRCh37.p13 chr6: 135,159,469-142,481,193	PBOV1, IFNGR1, 100 more genes
nsv6303442	copy number variation	1	nstd186	human		GRCh37 chr6: 135,526,212-135,527,307 , GRCh38.p12 chr6: 135,205,074-135,206,169	MYB, LOC105378011
nsv6290946	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 130,769,034-136,009,217 , GRCh38.p12 chr6: 130,447,889-135,688,079	LOC105378004, LINC01010, 89 more genes
nsv6135691	copy number variation	1	nstd213	human		GRCh37 chr6: 135,425,236-135,846,268 , GRCh38.p12 chr6: 135,104,098-135,525,130	MYB, AHI1, 5 more genes
nsv6135447	copy number variation	1	nstd213	human		GRCh37 chr6: 135,425,243-135,846,268 , GRCh38.p12 chr6: 135,104,105-135,525,130	MYB, AHI1, 5 more genes
nsv6112726	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 133,810,210-140,046,615 , GRCh38.p12 chr6: 133,489,072-139,725,478	SIMALR, MTFR2, 99 more genes
nsv5535770	insertion	1	nstd206	human		GRCh38 chr6: 135,181,137-135,181,158 , GRCh37.p13 chr6: 135,502,275-135,502,296	MYB
nsv5472145	copy number variation	1	nstd206	human		GRCh38 chr6: 135,205,074-135,206,169 , GRCh37.p13 chr6: 135,526,212-135,527,307	LOC105378011, MYB
nsv4826572	copy number variation	1	nstd200	human		GRCh37 chr6: 135,503,691-135,503,896 , GRCh38.p12 chr6: 135,182,553-135,182,758	MYB
nsv4675250	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 133,817,341-140,038,401 , GRCh38.p12 chr6: 133,496,203-139,717,264	ALDH8A1, IL22RA2, 99 more genes
nsv4606001	copy number variation	1	nstd183	human		GRCh37 chr6: 135,528,488-135,557,305 , GRCh38.p12 chr6: 135,207,350-135,236,167	LOC105378011, MYB

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Number of Variants: 20

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Organism

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Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Subject Phenotype Status

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Items: 1 to 20 of 144

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Number of Variants: 20

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