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Items: 6

The following term was not found in dbVar: personal.

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Number of Variants: 6

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3871517	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 103,335,671-103,389,222 , GRCh38 chr8: 102,323,443-102,376,994	UBR5
nsv6314244	complex chromosomal rearrangement	2	nstd102	human	Uncertain significance	GRCh37 chr3: 110,275,764-110,275,764 , GRCh37 chr3: 110,275,769-110,275,769 , GRCh38.p12 chr3: 110,556,917-110,556,917 , GRCh38.p12 chr3: 110,556,922-110,556,922 , GRCh38.p12 chr1: 198,107,007-198,107,007 , GRCh38.p12 chr1: 198,107,011-198,107,011 , GRCh37 chr1: 198,076,137-198,076,137 , GRCh37 chr1: 198,076,141-198,076,141	LOC105374037
nsv6314254	complex chromosomal rearrangement	13	nstd102	human	Pathogenic	GRCh37 chr2: 41,655,563-41,655,563 , GRCh37 chr2: 41,655,563-41,655,563 , GRCh37 chr2: 56,843,771-56,843,771 , GRCh37 chr2: 56,843,775-56,843,775 , GRCh37 chr2: 60,303,697-60,303,697 , GRCh37 chr2: 60,303,697-60,303,697 , GRCh37 chr5: 12,445,573-12,445,573 , GRCh37 chr5: 12,445,574-12,445,574 , GRCh37 chr5: 14,939,421-14,939,421 , GRCh37 chr5: 24,397,935-24,397,935 , GRCh37 chr7: 14,253,267-14,253,267 , GRCh37 chr5: 15,076,679-15,076,679 , GRCh37 chr5: 17,605,182-17,605,182 , GRCh37 chr5: 17,605,184-17,605,184 , GRCh37 chr5: 22,227,323-22,227,323 , GRCh37 chr7: 13,504,624-13,504,624 , GRCh37 chr7: 13,504,624-13,504,624 , GRCh37 chr7: 14,252,391-14,252,391 , GRCh37 chr5: 15,076,680-15,076,680 , GRCh37 chr5: 22,227,333-22,227,333 , GRCh37 chr7: 12,812,850-12,812,850 , GRCh37 chr7: 12,813,369-12,813,369 , GRCh37 chr5: 14,939,428-14,939,428 , GRCh37 chr5: 24,397,949-24,397,949 , GRCh37 chr7: 114,129,563-114,129,563 , GRCh37 chr7: 114,129,560-114,129,560 , GRCh38.p12 chr2: 41,428,423-41,428,423 , GRCh38.p12 chr2: 60,076,562-60,076,562 , GRCh38.p12 chr5: 14,939,312-14,939,312 , GRCh38.p12 chr5: 14,939,319-14,939,319 , GRCh38.p12 chr5: 17,605,073-17,605,073 , GRCh38.p12 chr5: 17,605,075-17,605,075 , GRCh38.p12 chr5: 22,227,214-22,227,214 , GRCh38.p12 chr5: 12,445,461-12,445,461 , GRCh38.p12 chr5: 12,445,462-12,445,462 , GRCh38.p12 chr5: 24,397,840-24,397,840 , GRCh38.p12 chr7: 12,773,744-12,773,744 , GRCh38.p12 chr7: 13,464,999-13,464,999 , GRCh38.p12 chr2: 56,616,636-56,616,636 , GRCh38.p12 chr2: 56,616,640-56,616,640 , GRCh38.p12 chr5: 15,076,570-15,076,570 , GRCh38.p12 chr5: 15,076,571-15,076,571 , GRCh38.p12 chr5: 22,227,224-22,227,224 , GRCh38.p12 chr7: 13,464,999-13,464,999 , GRCh38.p12 chr7: 114,489,505-114,489,505 , GRCh38.p12 chr7: 114,489,508-114,489,508 , GRCh38.p12 chr2: 41,428,423-41,428,423 , GRCh38.p12 chr2: 60,076,562-60,076,562 , GRCh38.p12 chr5: 24,397,826-24,397,826 , GRCh38.p12 chr7: 12,773,225-12,773,225 , GRCh38.p12 chr7: 14,212,766-14,212,766 , GRCh38.p12 chr7: 14,213,642-14,213,642	CDH12, DGKB, 5 more genes
nsv3872496	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 103,662,755-103,870,397 , GRCh38 chr8: 102,650,527-102,858,169	AZIN1, LOC105375686, 5 more genes
nsv3874754	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 22,308,420-24,492,723 , GRCh38.p12 chr5: 22,308,311-24,492,614	PRDM9, LOC503540, 14 more genes
nsv6314317	complex chromosomal rearrangement	2	nstd102	human	Uncertain significance	GRCh38.p12 chr4: 58,350,993-58,350,993 , GRCh38.p12 chr4: 58,350,998-58,350,998 , GRCh37 chr4: 59,217,159-59,217,159 , GRCh37 chr4: 59,217,164-59,217,164 , GRCh38.p12 chr1: 213,781,426-213,781,426 , GRCh38.p12 chr1: 213,781,437-213,781,437 , GRCh37 chr1: 213,954,769-213,954,769 , GRCh37 chr1: 213,954,780-213,954,780	0

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