klhl13[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
nsv6314325	complex chromosomal rearrangement	2	nstd102	human	Pathogenic	GRCh37 chrX: 44,901,361-44,901,361 , GRCh37 chrX: 117,134,725-117,134,725 , GRCh37 chrX: 117,140,815-117,140,815 , GRCh37 chrX: 44,893,800-44,893,800 , GRCh38.p12 chrX: 45,034,555-45,034,555 , GRCh38.p12 chrX: 45,042,116-45,042,116 , GRCh38.p12 chrX: 118,000,762-118,000,762 , GRCh38.p12 chrX: 118,006,852-118,006,852	KLHL13, KDM6A
nsv4728266	copy number variation	1	nstd102	human	Likely benign	GRCh37 chrX: 116,222,262-117,162,934 , GRCh38.p12 chrX: 117,088,294-118,028,971	KLHL13, TCERG1P1
nsv3902586	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chrX: 116,133,629-117,055,928 , GRCh38 chrX: 117,115,633-118,037,937 , GRCh37 chrX: 116,249,601-117,171,900	KLHL13, TCERG1P1
nsv3875835	copy number variation	1	nstd102	human	Likely benign	GRCh37 chrX: 115,996,197-117,104,069 , GRCh38.p12 chrX: 116,862,229-117,970,106	KLHL13, TCERG1P1, 1 more genes
nsv6313135	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 115,996,197-117,108,880 , GRCh38.p12 chrX: 116,862,229-117,974,917	KLHL13, TCERG1P1, 1 more genes
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	KLHL13, 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	KLHL13, 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	KLHL13, 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	KLHL13, 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	KLHL13, 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	KLHL13, 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	KLHL13, 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	KLHL13, 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	KLHL13, 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	KLHL13, 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	KLHL13, 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	KLHL13, 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	KLHL13, 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	KLHL13, 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	KLHL13, MIR934, 2151 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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