hydin[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
nsv3910122	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 70,929,925-71,196,477 , NCBI36 chr16: 69,487,426-69,753,978 , GRCh38 chr16: 70,896,022-71,162,574	HYDIN
nsv3911880	copy number variation	2	nstd102	human	Likely benign	GRCh38 chr16: 70,873,565-71,133,362 , NCBI36 chr16: 69,464,969-69,724,766 , GRCh37 chr16: 70,907,468-71,167,265	HYDIN
nsv3918450	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr16: 69,512,670-69,724,766 , GRCh37 chr16: 70,955,169-71,167,265 , GRCh38 chr16: 70,921,266-71,133,362	HYDIN
nsv3890485	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 70,983,768-71,201,052 , GRCh38.p12 chr16: 70,949,865-71,167,149	HYDIN
nsv1398546	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr16: 70,855,202-71,067,341 , GRCh37 chr16: 70,889,105-71,101,244	HYDIN
nsv3912563	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 70,860,486-71,196,477 , GRCh38 chr16: 70,826,583-71,162,574 , NCBI36 chr16: 69,417,987-69,753,978	HYDIN, RNU6ATAC25P
nsv3905340	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr16: 70,866,924-71,177,312 , GRCh38.p12 chr16: 70,833,021-71,143,409	HYDIN, RNU6ATAC25P
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	HYDIN, NECAB2, 219 more genes
nsv3917504	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 69,951,979-76,757,245 , NCBI36 chr16: 68,509,480-75,314,746 , GRCh38 chr16: 69,918,076-76,723,348	HYDIN, TRG-GCC3-1, 137 more genes
nsv3916803	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 68,126,727-74,517,697 , GRCh37.p13 chr16: 69,569,226-75,960,196 , GRCh38.p12 chr16: 69,535,323-75,926,298	HYDIN, AP1G1, 138 more genes
nsv6315469	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 68,971,067-74,823,560 , GRCh38.p12 chr16: 68,937,164-74,789,662	HYDIN, ZNF19, 128 more genes
nsv3911569	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 68,698,941-74,353,205 , NCBI36 chr16: 67,290,345-72,944,604 , GRCh37 chr16: 68,732,844-74,387,103	HYDIN, ATP5F1AP3, 121 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	HYDIN, 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	HYDIN, 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	HYDIN, 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	HYDIN, 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	HYDIN, 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	HYDIN, 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	HYDIN, 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	HYDIN, CFAP69P1, 716 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 62

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Number of Variants: 20

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Supplemental Content

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