adamts6[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
nsv3870677	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 64,604,303-64,604,800 , GRCh38.p12 chr5: 65,308,476-65,308,973	ADAMTS6
nsv3889848	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719	ADAMTS6, MEGF10, 2080 more genes
nsv6313676	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 64,049,692-70,306,646 , GRCh38.p12 chr5: 64,753,865-71,010,819	ADAMTS6, BCL9P1, 105 more genes
nsv3921568	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 64,228,590-68,791,331 , NCBI36 chr5: 64,264,346-68,827,087 , GRCh38 chr5: 64,932,763-69,495,504	ADAMTS6, LOC100419549, 67 more genes
nsv6312114	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 63,256,278-65,374,358 , GRCh38.p12 chr5: 63,960,451-66,078,530	ADAMTS6, RNF180, 23 more genes
nsv3886374	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028	ADAMTS6, LOC105374618, 2499 more genes
nsv3871533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343	ADAMTS6, PCDHGC5, 2492 more genes
nsv3875235	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788	ADAMTS6, SPEF2, 2490 more genes
nsv3911585	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 75,149-73,744,306 , GRCh38 chr5: 22,149-74,412,725 , GRCh37 chr5: 22,149-73,708,550	ADAMTS6, LINC02241, 878 more genes
nsv4578696	copy number variation	1	nstd102	human	Likely pathogenic	GRCh38 chr5: 58,780,641-73,523,380 , GRCh37.p13 chr5: 58,076,468-72,819,205	ADAMTS6, TRIM23, 215 more genes
nsv3916577	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr5: 64,745,346-65,762,306 , GRCh37 chr5: 64,709,590-65,726,550 , GRCh38 chr5: 65,413,763-66,430,722	ADAMTS6, TRIM23, 15 more genes
nsv6314399	complex chromosomal rearrangement	21	nstd102	human	Likely pathogenic	GRCh37 chr5: 64,591,846-64,591,846 , GRCh37 chr5: 66,440,749-66,440,749 , GRCh37 chr5: 67,083,502-67,083,502 , GRCh37 chr5: 68,034,033-68,034,033 , GRCh37 chr5: 75,288,962-75,288,962 , GRCh37 chr5: 75,288,966-75,288,966 , GRCh37 chr5: 83,549,447-83,549,447 , GRCh37 chr5: 86,770,057-86,770,057 , GRCh37 chr5: 87,602,314-87,602,314 , GRCh37 chr5: 87,604,093-87,604,093 , GRCh37 chr5: 93,895,937-93,895,937 , GRCh37 chr5: 62,504,815-62,504,815 , GRCh37 chr5: 64,591,964-64,591,964 , GRCh37 chr5: 83,549,442-83,549,442 , GRCh37 chr5: 84,532,816-84,532,816 , GRCh37 chr5: 86,636,063-86,636,063 , GRCh37 chr5: 86,636,066-86,636,066 , GRCh37 chr5: 88,329,135-88,329,135 , GRCh37 chr5: 94,502,031-94,502,031 , GRCh37 chr5: 63,593,860-63,593,860 , GRCh37 chr5: 63,670,571-63,670,571 , GRCh37 chr5: 64,591,845-64,591,845 , GRCh37 chr5: 64,936,581-64,936,581 , GRCh37 chr5: 66,440,749-66,440,749 , GRCh37 chr5: 68,034,032-68,034,032 , GRCh37 chr5: 84,532,817-84,532,817 , GRCh37 chr5: 85,220,098-85,220,098 , GRCh37 chr5: 62,504,816-62,504,816 , GRCh37 chr5: 64,936,580-64,936,580 , GRCh37 chr5: 67,048,551-67,048,551 , GRCh37 chr5: 67,083,162-67,083,162 , GRCh37 chr5: 84,762,134-84,762,134 , GRCh37 chr5: 84,762,134-84,762,134 , GRCh37 chr5: 85,220,098-85,220,098 , GRCh37 chr5: 86,770,160-86,770,160 , GRCh37 chr5: 87,441,218-87,441,218 , GRCh37 chr5: 93,895,935-93,895,935 , GRCh37 chr5: 94,502,031-94,502,031 , GRCh37 chr5: 94,670,198-94,670,198 , GRCh37 chr5: 94,670,198-94,670,198 , GRCh37 chr5: 87,441,161-87,441,161 , GRCh37 chr5: 88,329,131-88,329,131 , GRCh38.p12 chr5: 95,166,327-95,166,327 , GRCh38.p12 chr5: 64,298,033-64,298,033 , GRCh38.p12 chr5: 65,296,018-65,296,018 , GRCh38.p12 chr5: 67,144,921-67,144,921 , GRCh38.p12 chr5: 67,787,334-67,787,334 , GRCh38.p12 chr5: 85,466,316-85,466,316 , GRCh38.p12 chr5: 85,924,280-85,924,280 , GRCh38.p12 chr5: 87,474,343-87,474,343 , GRCh38.p12 chr5: 88,306,497-88,306,497 , GRCh38.p12 chr5: 89,033,318-89,033,318 , GRCh38.p12 chr5: 94,560,230-94,560,230 , GRCh38.p12 chr5: 94,560,232-94,560,232 , GRCh38.p12 chr5: 95,166,327-95,166,327 , GRCh38.p12 chr5: 95,334,494-95,334,494 , GRCh38.p12 chr5: 63,208,988-63,208,988 , GRCh38.p12 chr5: 65,296,137-65,296,137 , GRCh38.p12 chr5: 65,640,753-65,640,753 , GRCh38.p12 chr5: 84,253,624-84,253,624 , GRCh38.p12 chr5: 85,236,999-85,236,999 , GRCh38.p12 chr5: 85,466,316-85,466,316 , GRCh38.p12 chr5: 85,924,280-85,924,280 , GRCh38.p12 chr5: 88,145,401-88,145,401 , GRCh38.p12 chr5: 95,334,494-95,334,494 , GRCh38.p12 chr5: 64,374,744-64,374,744 , GRCh38.p12 chr5: 67,144,921-67,144,921 , GRCh38.p12 chr5: 75,993,137-75,993,137 , GRCh38.p12 chr5: 85,236,998-85,236,998 , GRCh38.p12 chr5: 87,340,249-87,340,249 , GRCh38.p12 chr5: 88,145,344-88,145,344 , GRCh38.p12 chr5: 88,308,276-88,308,276 , GRCh38.p12 chr5: 89,033,314-89,033,314 , GRCh38.p12 chr5: 63,208,989-63,208,989 , GRCh38.p12 chr5: 65,296,019-65,296,019 , GRCh38.p12 chr5: 65,640,754-65,640,754 , GRCh38.p12 chr5: 67,752,723-67,752,723 , GRCh38.p12 chr5: 67,787,674-67,787,674 , GRCh38.p12 chr5: 68,738,205-68,738,205 , GRCh38.p12 chr5: 68,738,206-68,738,206 , GRCh38.p12 chr5: 75,993,141-75,993,141 , GRCh38.p12 chr5: 84,253,629-84,253,629 , GRCh38.p12 chr5: 87,340,246-87,340,246 , GRCh38.p12 chr5: 87,474,240-87,474,240	ADAMTS6, CCNH, 12 more genes
nsv3883692	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr5: 58,966,132-68,847,066 , GRCh38.p12 chr5: 59,670,306-69,551,239	ADAMTS6, TRIM23, 125 more genes
nsv3920421	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr5: 62,538,695-70,622,774 , GRCh37 chr5: 62,502,939-70,587,018 , GRCh38 chr5: 63,207,112-71,291,191	ADAMTS6, TRIM23, 124 more genes
nsv3910901	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr5: 65,162,063-65,680,676 , NCBI36 chr5: 64,493,646-65,012,259 , GRCh37 chr5: 64,457,890-64,976,503	ADAMTS6, RPS2P23, 9 more genes
nsv4675585	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 64,775,928-64,994,289 , GRCh38.p12 chr5: 65,480,101-65,698,462	ADAMTS6, PPWD1, 6 more genes
nsv4436202	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379	ADAMTS6, RNU1-150P, 1757 more genes
nsv4729221	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 63,827,760-64,499,916 , GRCh38.p12 chr5: 64,531,933-65,204,089	ADAMTS6, SREK1IP1, 7 more genes
nsv3912593	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259	ADAMTS6, LOC105378993, 2492 more genes
nsv3916989	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr5: 64,543,311-66,078,345 , GRCh37 chr5: 64,507,555-66,042,589 , GRCh38 chr5: 65,211,728-66,746,761	ADAMTS6, LINC02229, 20 more genes

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Items: 20

Number of Variants: 20

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