klhl36[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
nsv3921095	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 69,005,977-83,499,227 , GRCh38 chr16: 70,414,573-84,908,120 , GRCh37 chr16: 70,448,476-84,941,726	KLHL36, NECAB2, 219 more genes
nsv3919844	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 78,704,275-87,819,342 , GRCh37 chr16: 78,738,172-87,852,948 , NCBI36 chr16: 77,295,673-86,410,449	KLHL36, RPL10AP12, 146 more genes
nsv3917609	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 80,344,868-84,305,898 , GRCh37 chr16: 81,787,367-85,748,397 , GRCh38 chr16: 81,753,762-85,714,791	KLHL36, LOC105371376, 63 more genes
nsv3911104	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 83,912,597-87,257,444 , GRCh38 chr16: 83,878,992-87,223,838 , NCBI36 chr16: 82,470,098-85,814,945	KLHL36, LOC101928557, 75 more genes
nsv3922440	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 82,278,756-84,664,347 , GRCh37 chr16: 83,721,255-86,106,846 , GRCh38 chr16: 83,687,650-86,073,240	KLHL36, LOC123862, 58 more genes
nsv3922490	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 83,016,872-85,087,809 , GRCh37 chr16: 83,050,477-85,121,415 , NCBI36 chr16: 81,607,978-83,678,916	KLHL36, MBTPS1, 33 more genes
nsv3922339	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 83,432,665-84,941,726 , GRCh38 chr16: 83,399,060-84,908,120 , NCBI36 chr16: 81,990,166-83,499,227	KLHL36, LOC648774, 28 more genes
nsv3906108	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224	KLHL36, CKLF, 1882 more genes
nsv3904593	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973	KLHL36, LOC100128079, 1879 more genes
nsv3901410	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287	KLHL36, LINC02175, 1877 more genes
nsv3909417	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867	KLHL36, PRSS53, 1868 more genes
nsv3892266	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654	KLHL36, FTLP14, 1868 more genes
nsv3921269	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345	KLHL36, LOC105371237, 985 more genes
nsv6314755	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654	KLHL36, ATMIN, 826 more genes
nsv3915506	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 51,490,596-88,682,563 , GRCh38 chr16: 52,899,183-90,088,654 , GRCh37 chr16: 52,933,095-90,155,062	KLHL36, CFAP69P1, 716 more genes
nsv3891306	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 57,051,473-89,797,669 , GRCh38.p12 chr16: 57,017,561-89,731,261	KLHL36, LOC107984894, 613 more genes
nsv3913913	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 62,980,782-88,675,894 , GRCh38 chr16: 64,389,378-90,081,985 , GRCh37 chr16: 64,423,281-90,148,393	KLHL36, ATP5F1AP3, 534 more genes
nsv3919817	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 63,904,799-88,675,894 , GRCh37 chr16: 65,347,298-90,148,393 , GRCh38 chr16: 65,313,395-90,081,985	KLHL36, LOC105376772, 527 more genes
nsv3910304	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 64,102,887-88,690,904 , GRCh38 chr16: 65,511,483-90,096,995 , GRCh37 chr16: 65,545,386-90,163,403	KLHL36, MC1R, 528 more genes
nsv3922616	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 70,514,631-90,081,985 , NCBI36 chr16: 69,106,035-88,675,894 , GRCh37 chr16: 70,548,534-90,148,393	KLHL36, FOXF1, 367 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 69

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Number of Variants: 20

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