nxt2[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
nsv3904162	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 10,001-156,030,895 , GRCh37 chrX: 60,001-155,260,560 , NCBI36 chrX: 1-154,913,754	NXT2, NANOGNBP3, 2154 more genes
nsv3913255	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chrX: 701-154,913,754 , GRCh37.p13 chrX: 60,701-155,260,560 , GRCh38.p12 chrX: 10,701-156,030,895	NXT2, NHS-AS1, 2154 more genes
nsv3907094	copy number variation	4	nstd102	human	Pathogenic	GRCh38 chrX: 10,679-156,022,206 , GRCh37 chrX: 60,679-155,251,871 , NCBI36 chrX: 679-154,905,065	NXT2, GPR119, 2153 more genes
nsv3878553	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chrX: 60,262-155,245,765 , GRCh38.p12 chrX: 10,262-156,016,100	NXT2, H2AB2, 2152 more genes
nsv3898149	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 20,297-156,026,127 , NCBI36 chrX: 10,297-154,908,986 , GRCh37 chrX: 70,297-155,255,792	NXT2, OR3B1P, 2154 more genes
nsv3877395	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 71,267-155,255,839 , GRCh38.p12 chrX: 21,267-156,026,174	NXT2, ARMCX2, 2154 more genes
nsv3884935	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 71,267-155,255,792 , GRCh38.p12 chrX: 21,267-156,026,127	NXT2, NDUFB11, 2154 more genes
nsv3903061	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chrX: 679-154,896,026 , GRCh38 chrX: 10,679-156,013,167 , GRCh37 chrX: 60,679-155,242,832	NXT2, SLC38A5, 2152 more genes
nsv3885865	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 70,297-155,246,585 , GRCh38.p12 chrX: 20,297-156,016,920	NXT2, MIR1277, 2152 more genes
nsv6112690	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301	NXT2, LOC105373176, 2151 more genes
nsv3907545	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 64,245-155,228,958 , NCBI36 chrX: 4,245-154,882,152 , GRCh38 chrX: 14,245-155,999,293	NXT2, TMEM30BP1, 2151 more genes
nsv3884029	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 71,267-155,224,766 , GRCh38.p12 chrX: 21,267-155,995,101	NXT2, SSX4B, 2150 more genes
nsv3898185	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chrX: 76,102-155,226,096 , NCBI36 chrX: 16,102-154,879,290 , GRCh38 chrX: 26,102-155,996,431	NXT2, ANKRD11P2, 2151 more genes
nsv3891981	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 10,701-155,978,689 , NCBI36 chrX: 701-154,861,548 , GRCh37 chrX: 60,701-155,208,354	NXT2, PAICSP7, 2149 more genes
nsv3892026	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 40,904-155,998,166 , GRCh37 chrX: 90,904-155,227,831 , NCBI36 chrX: 30,904-154,881,025	NXT2, MIR934, 2151 more genes
nsv3903163	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chrX: 168,546-155,233,731 , GRCh38 chrX: 251,879-156,004,066 , NCBI36 chrX: 108,546-154,886,925	NXT2, RPL36A, 2151 more genes
nsv3887722	copy number variation	4	nstd102	human	Pathogenic	GRCh37 chrX: 168,546-155,233,731 , GRCh38.p12 chrX: 251,879-156,004,066	NXT2, CT45A3, 2151 more genes
nsv3901047	copy number variation	3	nstd102	human	Pathogenic, conflicting data from submitters	GRCh38 chrX: 251,880-156,004,066 , GRCh37 chrX: 168,547-155,233,731 , NCBI36 chrX: 108,547-154,886,925	NXT2, GPR119, 2151 more genes
nsv3890023	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chrX: 70,140-154,929,279 , NCBI36 chrX: 10,140-154,582,473 , GRCh38 chrX: 20,140-155,699,618	NXT2, MIRLET7F2, 2145 more genes
nsv3885965	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 181,779-155,171,702 , GRCh38.p12 chrX: 265,112-155,942,038	NXT2, ZFYVE9P1, 2148 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 159

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Number of Variants: 20

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Supplemental Content

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Search details

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