natd1[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 14

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Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3890462	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 17,200,426-21,900,910 , GRCh38.p12 chr17: 17,297,112-22,374,304	NATD1, LOC100132977, 179 more genes
nsv3903684	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004	NATD1, MIR3185, 2366 more genes
nsv3899740	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564	NATD1, P4HB, 2366 more genes
nsv3906245	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251	NATD1, MIR21, 2366 more genes
nsv3907261	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062	NATD1, SMURF2, 2366 more genes
nsv3914783	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577	NATD1, LOC105371922, 1855 more genes
nsv6315238	complex substitution	1	nstd102	human	Pathogenic	GRCh37 chr17: 14,876,984-22,124,952 , GRCh38.p12 chr17: 14,973,667-22,625,625	NATD1, ADORA2B, 281 more genes
nsv3890477	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 20,775,032-21,545,209 , GRCh38.p12 chr17: 20,871,719-21,641,964	NATD1, MAP2K3, 19 more genes
nsv3922250	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr17: 20,935,766-21,621,469 , GRCh37 chr17: 20,839,079-21,529,632 , NCBI36 chr17: 20,779,671-21,471,956	NATD1, LOC101930665, 15 more genes
nsv3912785	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr17: 19,070,690-21,619,442 , GRCh37 chr17: 18,974,003-21,522,709 , NCBI36 chr17: 18,914,728-21,463,302	NATD1, TMEM11-DT, 96 more genes
nsv3903546	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 20,465,210-22,261,792 , GRCh38.p12 chr17: 20,561,897-22,762,465	NATD1, LOC105371589, 62 more genes
nsv3922944	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr17: 19,587,938-21,442,522 , GRCh37 chr17: 19,647,346-21,501,929 , GRCh38 chr17: 19,744,033-21,598,663	NATD1, RNU6-258P, 61 more genes
nsv3895897	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 20,741,728-22,060,092 , GRCh38.p12 chr17: 20,838,415-22,560,765	NATD1, MTND6P34, 45 more genes
nsv3916846	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr17: 20,723,331-21,956,890 , GRCh38 chr17: 20,879,426-22,533,437 , GRCh37 chr17: 20,782,739-22,032,763	NATD1, PDLIM1P2, 44 more genes

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