baat[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
nsv3917989	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 102,112,198-118,529,754 , NCBI36 chr9: 101,152,019-117,569,575 , GRCh38 chr9: 99,349,916-115,767,475	BAAT, CTNNAL1, 262 more genes
nsv3922633	copy number variation	2	nstd102	human	Pathogenic	GRCh38 chr9: 99,138,048-115,011,033 , NCBI36 chr9: 100,940,151-116,813,133 , GRCh37 chr9: 101,900,330-117,773,312	BAAT, RAD23B, 262 more genes
nsv3922551	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 95,061,030-108,695,569 , NCBI36 chr9: 96,863,133-110,497,670 , GRCh37 chr9: 97,823,312-111,457,849	BAAT, HEMGN, 243 more genes
nsv6315179	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 93,864,974-106,661,581 , GRCh38.p12 chr9: 91,102,692-103,899,300	BAAT, SUGT1P4-STRA6LP, 255 more genes
nsv4684256	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 96,126,075-108,535,272 , GRCh38.p12 chr9: 93,363,793-105,772,991	BAAT, RPS26P37, 238 more genes
nsv3910258	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 99,024,205-109,947,890 , GRCh37 chr9: 101,786,487-112,710,170 , NCBI36 chr9: 100,826,308-111,749,991	BAAT, LOC105376191, 167 more genes
nsv3891403	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 103,271,401-113,948,226 , GRCh38.p12 chr9: 100,509,119-111,185,946	BAAT, LOC112268038, 158 more genes
nsv5381561	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 97,834,573-107,199,088 , GRCh38.p12 chr9: 95,072,291-104,436,807	BAAT, TBC1D2, 170 more genes
nsv7097677	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 104,124,710-104,500,261 , GRCh38.p12 chr9: 101,362,428-101,737,979	BAAT, TMEM246-AS1, 10 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	BAAT, ALOX15P2, 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	BAAT, TBC1D13, 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	BAAT, MIR219A2, 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	BAAT, OR13C1P, 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	BAAT, RPL19P15, 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	BAAT, BANCR, 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	BAAT, OR2AM1P, 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	BAAT, TDRD7, 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	BAAT, LOC107987031, 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	BAAT, CTNNAL1, 2170 more genes
nsv3911025	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 193,412-138,124,524 , NCBI36 chr9: 194,090-140,138,797 , GRCh37 chr9: 204,090-141,018,976	BAAT, RORB-AS1, 2168 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 37

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Number of Variants: 20

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Supplemental Content

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