adgb[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
nsv6314616	complex chromosomal rearrangement	3	nstd102	human	Uncertain significance	GRCh37 chr6: 146,998,534-146,998,534 , GRCh37 chr11: 97,119,538-97,119,538 , GRCh37 chr11: 98,571,927-98,571,927 , GRCh37 chr11: 98,571,927-98,571,927 , GRCh37 chr6: 146,998,514-146,998,514 , GRCh37 chr11: 97,119,538-97,119,538 , GRCh38.p12 chr11: 97,248,538-97,248,538 , GRCh38.p12 chr11: 98,701,197-98,701,197 , GRCh38.p12 chr11: 97,248,538-97,248,538 , GRCh38.p12 chr6: 146,677,398-146,677,398 , GRCh38.p12 chr6: 146,677,378-146,677,378 , GRCh38.p12 chr11: 98,701,197-98,701,197	ADGB
nsv3893764	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 146,880,407-146,988,998 , GRCh38.p12 chr6: 146,559,271-146,667,862	ADGB, ADGB-DT
nsv3883927	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 146,735,206-147,036,914 , GRCh38 chr6: 146,414,070-146,715,778	ADGB, RAB32, 2 more genes
nsv3919835	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr6: 146,844,177-146,975,794 , GRCh37.p13 chr6: 146,802,484-146,934,101 , GRCh38.p12 chr6: 146,481,348-146,612,965	ADGB, ADGB-DT, 1 more genes
nsv4729399	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 146,872,465-146,991,066 , GRCh38.p12 chr6: 146,551,329-146,669,930	ADGB, RAB32, 1 more genes
nsv4350212	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 135,239,633-146,997,510 , GRCh38.p12 chr6: 134,918,495-146,676,374	ADGB, LOC100131041, 146 more genes
nsv3891146	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 139,513,020-150,389,231 , GRCh38.p12 chr6: 139,191,883-150,068,095	ADGB, UST, 131 more genes
nsv3890752	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 144,075,695-152,337,005 , GRCh38.p12 chr6: 143,754,558-152,015,870	ADGB, LOC105378052, 109 more genes
nsv3920651	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 144,932,561-152,985,364 , NCBI36 chr6: 145,295,390-153,348,192 , GRCh37 chr6: 145,253,697-153,306,499	ADGB, PPP1R14C, 107 more genes
nsv3904637	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 144,947,731-150,266,155 , GRCh38.p12 chr6: 144,626,595-149,945,019	ADGB, LOC107986660, 59 more genes
nsv3910985	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 146,843,948-151,790,457 , GRCh37 chr6: 146,802,255-151,748,764 , GRCh38 chr6: 146,481,119-151,427,629	ADGB, RMND1, 77 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	ADGB, LOC105378061, 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	ADGB, RNU6-411P, 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	ADGB, SOD1P1, 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	ADGB, ITPR3, 2905 more genes
nsv3911993	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 133,900,102-166,209,023 , GRCh38 chr6: 133,537,271-165,875,545 , GRCh37 chr6: 133,858,409-166,289,033	ADGB, LOC105369171, 418 more genes
nsv3915150	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 124,322,082-156,156,864 , GRCh37.p13 chr6: 124,280,383-156,115,172 , GRCh38.p12 chr6: 123,959,238-155,794,038	ADGB, KATNA1, 422 more genes
nsv3920975	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 141,454,127-169,739,666 , GRCh38 chr6: 141,132,990-169,339,571 , NCBI36 chr6: 141,495,820-169,481,591	ADGB, UST-AS2, 394 more genes
nsv3911164	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 135,720,981-155,817,943 , GRCh37 chr6: 135,679,288-155,776,251 , GRCh38 chr6: 135,358,150-155,455,117	ADGB, HYMAI, 263 more genes
nsv3898363	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 146,652,354-148,108,890 , GRCh38.p12 chr6: 146,331,218-147,787,754	ADGB, LUADT1, 12 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 21

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Number of Variants: 20

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