mthfd1[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 16

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7093055	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr14: 64,892,873-64,892,973 , GRCh38 chr14: 64,426,155-64,426,255	MTHFD1
nsv6309354	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 64,902,267-64,916,360 , GRCh38.p12 chr14: 64,435,549-64,449,642	MTHFD1, ZBTB25
nsv3922652	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 57,507,754-67,674,948 , NCBI36 chr14: 56,577,507-66,744,701 , GRCh38 chr14: 57,041,036-67,208,231	MTHFD1, PARP1P2, 160 more genes
nsv3923965	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 60,383,769-67,217,521 , NCBI36 chr14: 59,453,522-66,287,274 , GRCh38 chr14: 59,917,051-66,750,803	MTHFD1, ESR2, 111 more genes
nsv3912530	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr14: 61,789,171-65,289,887 , GRCh38 chr14: 62,252,700-65,753,416 , GRCh37 chr14: 62,719,418-66,220,134	MTHFD1, MIR625, 59 more genes
nsv3902883	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,000,422-107,289,053 , GRCh38.p12 chr14: 18,223,945-106,880,863	MTHFD1, LOC440181, 1998 more genes
nsv3907460	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,280,733-107,287,663 , GRCh38.p12 chr14: 18,504,256-106,879,456	MTHFD1, BANF1P1, 1996 more genes
nsv3899639	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,327,823-107,287,663 , GRCh38.p12 chr14: 18,551,346-106,879,456	MTHFD1, LOC100289511, 1996 more genes
nsv3903256	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,794,561-107,234,280 , GRCh38.p12 chr14: 19,652,445-106,826,050	MTHFD1, DHRS7, 1946 more genes
nsv3919106	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,511,673-107,285,437 , GRCh38 chr14: 20,043,514-106,877,229 , NCBI36 chr14: 19,581,513-106,356,482	MTHFD1, SRMP2, 1929 more genes
nsv3904265	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,511,673-107,285,437 , GRCh38.p12 chr14: 20,043,514-106,877,229	MTHFD1, CRIP1, 1929 more genes
nsv3917422	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 20,151,149-106,855,263 , NCBI36 chr14: 19,689,148-106,334,523 , GRCh37 chr14: 20,619,308-107,263,478	MTHFD1, MIR656, 1918 more genes
nsv6315524	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013	MTHFD1, PAPOLA-DT, 1338 more genes
nsv5980451	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr14: 54,654,001-75,828,024 , GRCh38.p12 chr14: 54,187,283-75,361,321	MTHFD1, ACTN1, 400 more genes
nsv4729599	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr14: 61,409,856-65,742,610 , GRCh38.p12 chr14: 60,943,138-65,275,892	MTHFD1, PARP1P2, 73 more genes
nsv6315477	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 64,016,496-65,834,490 , GRCh38.p12 chr14: 63,549,778-65,367,772	MTHFD1, LOC105370534, 43 more genes

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