btbd9[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 18

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3874740	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 38,391,668-38,404,140 , GRCh38.p12 chr6: 38,423,892-38,436,364	BTBD9
nsv3879503	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 38,497,963-38,504,204 , GRCh38.p12 chr6: 38,530,187-38,536,428	BTBD9
nsv3874057	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 38,240,318-38,435,497 , GRCh38.p12 chr6: 38,272,542-38,467,721	BTBD9
nsv4455521	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 38,140,596-38,324,813 , GRCh38.p12 chr6: 38,172,820-38,357,037	BTBD9, LOC105375045
nsv3879384	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 38,454,828-38,581,039 , GRCh38.p12 chr6: 38,487,052-38,613,263	BTBD9, TFGP1
nsv6636488	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 38,454,829-38,581,039 , GRCh38.p12 chr6: 38,487,053-38,613,263	BTBD9, TFGP1
nsv3919034	copy number variation	1	nstd102	human	Benign	NCBI36 chr6: 38,157,563-38,710,042 , GRCh37 chr6: 38,049,585-38,602,064 , GRCh38 chr6: 38,081,809-38,634,288	BTBD9, TFGP1, 3 more genes
nsv4455717	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 38,174,820-38,605,375 , GRCh38.p12 chr6: 38,207,044-38,637,599	BTBD9, BTBD9-AS1, 2 more genes
nsv4456836	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 38,382,510-38,658,257 , GRCh38.p12 chr6: 38,414,734-38,690,481	BTBD9, BTBD9-AS1, 3 more genes
nsv3919521	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 37,853,123-45,729,558 , GRCh37 chr6: 37,745,145-45,621,580 , GRCh38 chr6: 37,777,369-45,653,843	BTBD9, RPL23P6, 184 more genes
nsv5200371	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 34,401,304-38,435,497 , GRCh38.p12 chr6: 34,433,527-38,467,721	BTBD9, RPS15AP19, 95 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	BTBD9, 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	BTBD9, 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	BTBD9, 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	BTBD9, ITPR3, 2905 more genes
nsv4350067	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650	BTBD9, HLA-DPB2, 1001 more genes
nsv3913920	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028	BTBD9, TRR-ACG1-2, 1385 more genes
nsv6290922	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 37,485,973-38,275,476 , GRCh38.p12 chr6: 37,518,197-38,307,700	BTBD9, RN7SL285P, 7 more genes

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