bhmt[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
nsv3889988	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 78,397,980-78,436,211 , GRCh38.p12 chr5: 79,102,157-79,140,388	BHMT
nsv3887484	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 78,397,980-78,427,208 , GRCh38.p12 chr5: 79,102,157-79,131,385	BHMT
nsv6291284	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 78,406,853-78,524,612 , GRCh38.p12 chr5: 79,111,030-79,228,789	BHMT, RNY3P1
nsv3917452	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr5: 78,359,987-78,526,637 , GRCh38 chr5: 79,028,408-79,195,058 , GRCh37 chr5: 78,324,231-78,490,881	BHMT, DMGDH, 2 more genes
nsv6291177	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 78,196,511-78,445,636 , GRCh38.p12 chr5: 78,900,688-79,149,813	BHMT, LOC100505796, 3 more genes
nsv3889848	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719	BHMT, MEGF10, 2080 more genes
nsv3886374	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028	BHMT, LOC105374618, 2499 more genes
nsv3871533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343	BHMT, PCDHGC5, 2492 more genes
nsv3875235	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788	BHMT, SPEF2, 2490 more genes
nsv3917856	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 74,163,186-110,809,453 , NCBI36 chr5: 73,494,767-110,173,052 , GRCh37 chr5: 73,459,011-110,145,153	BHMT, CSNK1A1P3, 413 more genes
nsv4675667	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 72,790,061-97,478,870 , GRCh38.p12 chr5: 73,494,236-98,143,166	BHMT, LOC101929380, 318 more genes
nsv3877842	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 78,265,041-78,558,425 , GRCh38.p12 chr5: 78,969,218-79,262,602	BHMT, BHMT2, 5 more genes
nsv4436202	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379	BHMT, RNU1-150P, 1757 more genes
nsv6636260	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 77,746,948-79,089,197 , GRCh38.p12 chr5: 78,451,125-79,793,374	BHMT, RPL29P15, 18 more genes
nsv3924413	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr5: 78,393,035-78,796,005 , GRCh37.p13 chr5: 78,357,279-78,760,249 , GRCh38.p12 chr5: 79,061,456-79,464,426	BHMT, JMY, 7 more genes
nsv4456679	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr5: 78,323,433-78,693,915 , GRCh38.p12 chr5: 79,027,610-79,398,092	BHMT, JMY, 7 more genes
nsv4455120	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 78,324,437-78,693,659 , GRCh38.p12 chr5: 79,028,614-79,397,836	BHMT, BHMT2, 7 more genes
nsv4675083	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 78,366,704-78,689,771 , GRCh38.p12 chr5: 79,070,881-79,393,948	BHMT, RPS3AP20, 6 more genes
nsv4675123	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 78,401,788-78,708,407 , GRCh38.p12 chr5: 79,105,965-79,412,584	BHMT, LOC102724530, 5 more genes
nsv4675296	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 78,366,704-78,651,243 , GRCh38.p12 chr5: 79,070,881-79,355,420	BHMT, BHMT2, 5 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 26

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Number of Variants: 20

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