cxxc1[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
nsv6314722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 1,262,334-53,254,751 , GRCh38.p12 chr18: 1,262,333-55,587,520	CXXC1, LOC107985176, 632 more genes
nsv3902831	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 46,177,798-78,014,123 , GRCh38.p12 chr18: 48,651,427-80,256,240	CXXC1, LOC105372180, 370 more genes
nsv3906152	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 46,942,427-78,014,123 , GRCh38.p12 chr18: 49,416,057-80,256,240	CXXC1, RPL17P44, 360 more genes
nsv3909519	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 47,656,799-78,014,123 , GRCh38.p12 chr18: 50,130,429-80,256,240	CXXC1, LOC105372160, 339 more genes
nsv6315530	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271	CXXC1, LOC105372145, 947 more genes
nsv3907444	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 12,842-78,015,180 , GRCh38.p12 chr18: 12,842-80,257,297	CXXC1, GALNT1, 947 more genes
nsv3890669	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 13,034-78,015,180 , GRCh38.p12 chr18: 13,034-80,257,297	CXXC1, MYL12B, 947 more genes
nsv3918488	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 43,345-76,068,860 , GRCh38 chr18: 53,345-80,209,986 , GRCh37 chr18: 53,345-77,967,869	CXXC1, LOC105372027, 945 more genes
nsv3924351	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 108,760-76,113,817 , GRCh38 chr18: 118,760-80,254,946 , GRCh37 chr18: 118,760-78,012,829	CXXC1, MIX23P1, 942 more genes
nsv3919004	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr18: 136,226-80,256,240 , GRCh37 chr18: 136,226-78,014,123 , NCBI36 chr18: 126,226-76,115,097	CXXC1, LIVAR, 941 more genes
nsv3899451	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 136,226-78,014,123 , GRCh38.p12 chr18: 136,226-80,256,240	CXXC1, BOLA2P1, 941 more genes
nsv3924706	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 136,227-78,014,123 , GRCh38 chr18: 136,227-80,256,240 , NCBI36 chr18: 126,227-76,115,097	CXXC1, LOC100420948, 941 more genes
nsv3907722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 136,227-78,014,123 , GRCh38.p12 chr18: 136,227-80,256,240	CXXC1, ROCK1, 941 more genes
nsv3910887	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 139,089-76,113,807 , GRCh37 chr18: 149,089-78,012,819 , GRCh38 chr18: 149,089-80,254,936	CXXC1, LPIN2, 941 more genes
nsv3912925	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr18: 138,963-76,111,023 , GRCh38 chr18: 148,963-80,252,149 , GRCh37 chr18: 148,963-78,010,032	CXXC1, LOC105372038, 941 more genes
nsv3923838	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 138,963-76,103,255 , GRCh37 chr18: 148,963-78,002,264 , GRCh38 chr18: 148,963-80,244,381	CXXC1, WDR7-OT1, 941 more genes
nsv3916426	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 149,089-77,992,274 , NCBI36 chr18: 139,089-76,093,265 , GRCh38 chr18: 149,089-80,234,391	CXXC1, TPGS2, 941 more genes
nsv3890705	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 163,323-78,005,236 , GRCh38.p12 chr18: 163,323-80,247,353	CXXC1, RAX, 940 more genes
nsv3895186	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 163,323-78,005,185 , GRCh38.p12 chr18: 163,323-80,247,302	CXXC1, CLUL1, 940 more genes
nsv3890564	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 14,869,204-78,014,123 , GRCh38.p12 chr18: 14,869,205-80,256,240	CXXC1, LOC105372046, 683 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 44

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Number of Variants: 20

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Supplemental Content

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Search details

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