hh[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
nsv3890445	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 89,558,064-89,562,136 , GRCh38.p12 chr9: 86,943,149-86,947,221	GAS1, GAS1RR
nsv3890085	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 89,560,889-89,562,136 , GRCh38.p12 chr9: 86,945,974-86,947,221	GAS1RR, GAS1
nsv3897005	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 89,554,097-89,574,128 , GRCh38.p12 chr9: 86,939,182-86,959,213	GAS1, GAS1RR
nsv3903282	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 89,560,889-89,574,128 , GRCh38.p12 chr9: 86,945,974-86,959,213	GAS1RR, GAS1
nsv3915533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 88,694,766-94,589,503 , NCBI36 chr9: 87,884,586-93,629,324 , GRCh38 chr9: 86,079,851-91,827,221	SPIN1, PAICSP2, 98 more genes
nsv6290728	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 26,008,259-26,168,230 , GRCh38.p12 chr6: 26,008,031-26,168,002	H2BC3, H1-1, 18 more genes
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	LOC105378061, MIR4640, 2914 more genes
nsv3879811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083	RNU6-411P, LOC107986611, 2910 more genes
nsv3887898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394	SOD1P1, HLA-DPB1, 2905 more genes
nsv3889814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382	ITPR3, HSD17B8, 2905 more genes
nsv3912247	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 2,934-140,273,252 , GRCh37.p13 chr9: 12,934-141,153,431 , GRCh38.p12 chr9: 12,934-138,262,981	ALOX15P2, LOC107987061, 2184 more genes
nsv3890420	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,122,247 , GRCh38.p12 chr9: 10,590-138,231,797	TBC1D13, LOC105376186, 2183 more genes
nsv3905118	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,114,095 , GRCh38.p12 chr9: 10,590-138,223,645	MIR219A2, CLCN3P1, 2183 more genes
nsv3891842	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,107,672 , GRCh38.p12 chr9: 10,590-138,217,222	OR13C1P, CDC37L1, 2183 more genes
nsv3895453	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 46,587-141,066,491 , GRCh38.p12 chr9: 46,587-138,172,039	RPL19P15, SPATA31D5P, 2176 more genes
nsv3900967	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 163,131-141,122,114 , GRCh38.p12 chr9: 163,131-138,231,664	BANCR, SETX, 2173 more genes
nsv3907479	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 62,525-141,006,407 , GRCh38.p12 chr9: 62,525-138,111,955	OR2AM1P, RN7SL565P, 2174 more genes
nsv3922684	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897	TDRD7, CDK9, 2170 more genes
nsv3919257	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 204,193-141,073,897 , GRCh38 chr9: 204,193-138,179,445 , NCBI36 chr9: 194,193-140,193,718	LOC107987031, LOC105376234, 2169 more genes
nsv3915973	copy number variation	2	nstd102	human	Pathogenic	GRCh38 chr9: 193,412-138,159,073 , GRCh37 chr9: 68,420,641-141,053,525 , NCBI36 chr9: 67,910,461-140,173,346	CTNNAL1, QSOX2, 2170 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 66

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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