stenotic lesion - dbVar - NCBI

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Items: 4

The following term was not found in dbVar: stenotic.

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Number of Variants: 4

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6314612	complex chromosomal rearrangement	2	nstd102	human	Uncertain significance	GRCh38.p12 chr19: 38,472,137-38,472,137 , GRCh38.p12 chr19: 38,472,144-38,472,144 , GRCh37 chr19: 38,962,777-38,962,777 , GRCh37 chr19: 38,962,784-38,962,784 , GRCh38.p12 chr9: 96,045,206-96,045,206 , GRCh38.p12 chr9: 96,045,209-96,045,209 , GRCh37 chr9: 98,807,488-98,807,488 , GRCh37 chr9: 98,807,491-98,807,491	RYR1
nsv6314485	complex chromosomal rearrangement	3	nstd102	human	Uncertain significance	GRCh37 chrX: 154,390,213-154,390,213 , GRCh37 chrX: 655,195-655,195 , GRCh37 chrX: 698,367-698,367 , GRCh37 chrX: 135,300,329-135,300,329 , GRCh37 chrX: 135,300,418-135,300,418 , GRCh37 chrX: 154,388,192-154,388,192 , GRCh38.p12 chrX: 694,460-694,460 , GRCh38.p12 chrX: 737,632-737,632 , GRCh38.p12 chrX: 136,218,170-136,218,170 , GRCh38.p12 chrX: 136,218,259-136,218,259 , GRCh38.p12 chrX: 155,159,917-155,159,917 , GRCh38.p12 chrX: 155,161,938-155,161,938	MAP7D3
nsv6314583	complex chromosomal rearrangement	2	nstd102	human	Uncertain significance	GRCh37 chrX: 141,915,776-141,915,776 , GRCh37 chrX: 141,922,633-141,922,633 , GRCh37 chrX: 154,060,808-154,060,808 , GRCh37 chrX: 154,066,467-154,066,467 , GRCh38.p12 chrX: 142,827,990-142,827,990 , GRCh38.p12 chrX: 142,834,847-142,834,847 , GRCh38.p12 chrX: 154,832,533-154,832,533 , GRCh38.p12 chrX: 154,838,192-154,838,192	F8, SMIM9
nsv6314506	complex chromosomal rearrangement	7	nstd102	human	Uncertain significance	GRCh37 chr6: 21,715,677-21,715,677 , GRCh37 chr6: 21,715,677-21,715,677 , GRCh37 chr6: 83,891,695-83,891,695 , GRCh37 chr6: 123,834,806-123,834,806 , GRCh37 chr6: 78,967,194-78,967,194 , GRCh37 chr6: 79,036,476-79,036,476 , GRCh37 chr6: 123,834,803-123,834,803 , GRCh37 chr6: 83,891,695-83,891,695 , GRCh37 chr6: 127,919,515-127,919,515 , GRCh37 chr6: 128,030,235-128,030,235 , GRCh37 chr6: 84,496,838-84,496,838 , GRCh37 chr6: 84,496,838-84,496,838 , GRCh37 chr13: 57,178,494-57,178,494 , GRCh37 chr13: 57,178,506-57,178,506 , GRCh38.p12 chr6: 78,257,477-78,257,477 , GRCh38.p12 chr6: 78,326,759-78,326,759 , GRCh38.p12 chr6: 83,181,976-83,181,976 , GRCh38.p12 chr6: 83,787,119-83,787,119 , GRCh38.p12 chr6: 123,513,661-123,513,661 , GRCh38.p12 chr6: 21,715,446-21,715,446 , GRCh38.p12 chr6: 21,715,446-21,715,446 , GRCh38.p12 chr6: 127,598,370-127,598,370 , GRCh38.p12 chr6: 127,709,090-127,709,090 , GRCh38.p12 chr6: 83,181,976-83,181,976 , GRCh38.p12 chr6: 83,787,119-83,787,119 , GRCh38.p12 chr6: 123,513,658-123,513,658 , GRCh38.p12 chr13: 56,604,360-56,604,360 , GRCh38.p12 chr13: 56,604,372-56,604,372 , GRCh38.p12 chr6\|NT_187556.1: 54,288-54,288	CASC15, PGM3, 5 more genes

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