nr5a1[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
nsv4681126	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 127,243,637-127,267,690 , GRCh38.p12 chr9: 124,481,358-124,505,411	NR5A1
nsv7093083	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 127,253,202-127,253,433 , GRCh38 chr9: 124,490,923-124,491,154	NR5A1
nsv997182	copy number variation	1	nstd45	human	Pathogenic	GRCh38.p12 chr9: 124,481,236-124,507,420 , GRCh37 chr9: 127,243,515-127,269,699	NR5A1
nsv3889405	copy number variation	2	nstd102	human	Likely pathogenic	GRCh37 chr9: 127,244,699-127,245,207 , GRCh38 chr9: 124,482,420-124,482,928	NR5A1
nsv3891259	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 127,253,558-127,254,078 , GRCh38.p12 chr9: 124,491,279-124,491,799	NR5A1
nsv3901498	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 127,264,913-127,269,352 , GRCh38.p12 chr9: 124,502,634-124,507,073	NR5A1
nsv3897456	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr9: 127,269,352-127,294,297 , GRCh38.p12 chr9: 124,507,073-124,532,018	NR5A1, NR6A1
nsv6314530	complex chromosomal rearrangement	4	nstd102	human	Pathogenic	GRCh37 chr9: 100,194,180-100,194,180 , GRCh37 chr9: 100,195,366-100,195,366 , GRCh37 chr9: 126,738,625-126,738,625 , GRCh37 chr9: 126,741,394-126,741,394 , GRCh37 chr9: 126,753,305-126,753,305 , GRCh37 chr9: 126,756,206-126,756,206 , GRCh37 chr9: 127,266,258-127,266,258 , GRCh37 chr9: 127,266,339-127,266,339 , GRCh38.p12 chr9: 97,431,898-97,431,898 , GRCh38.p12 chr9: 97,433,084-97,433,084 , GRCh38.p12 chr9: 123,976,346-123,976,346 , GRCh38.p12 chr9: 123,979,115-123,979,115 , GRCh38.p12 chr9: 123,991,026-123,991,026 , GRCh38.p12 chr9: 123,993,927-123,993,927 , GRCh38.p12 chr9: 124,503,979-124,503,979 , GRCh38.p12 chr9: 124,504,060-124,504,060	NR5A1, TDRD7, 1 more genes
nsv3900377	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 127,204,712-127,267,689 , GRCh38.p12 chr9: 124,442,433-124,505,410	NR5A1, ADGRD2, 1 more genes
nsv6291398	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 120,045,175-127,335,905 , GRCh38.p12 chr9: 117,282,896-124,573,626	NR5A1, ZBTB6, 107 more genes
nsv6637981	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 124,018,736-129,995,568 , GRCh38.p12 chr9: 121,256,458-127,233,289	NR5A1, PBX3-DT, 119 more genes
nsv3922263	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 124,897,698-128,495,943 , GRCh38 chr9: 123,095,598-126,693,843 , GRCh37 chr9: 125,857,877-129,456,122	NR5A1, OLFML2A, 64 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	NR5A1, 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	NR5A1, 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	NR5A1, 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	NR5A1, 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	NR5A1, 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	NR5A1, 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	NR5A1, 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	NR5A1, TDRD7, 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 39

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Number of Variants: 20

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