ClinVar Miner

Submissions for variant GRCh38/hg38 7q11.1-11.21(chr7:61006478-62410831)x1

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Total submissions: 9
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ISCA site 1 RCV000135726 SCV000175637 pathogenic See cases 2018-02-14 no assertion criteria provided clinical testing
ISCA site 1 RCV000137175 SCV000177381 pathogenic See cases 2018-02-14 no assertion criteria provided clinical testing
ISCA site 4 RCV000148182 SCV000077573 benign See cases 2011-08-12 criteria provided, single submitter clinical testing
ISCA site 4 RCV000050887 SCV000078220 benign See cases 2011-08-12 criteria provided, single submitter clinical testing
ISCA site 4 RCV000050266 SCV000172979 benign See cases 2013-08-05 no assertion criteria provided clinical testing
ISCA site 4 RCV000142473 SCV000174285 pathogenic See cases 2010-07-30 no assertion criteria provided clinical testing
ISCA site 4 RCV000134814 SCV000174418 benign See cases 2010-10-30 no assertion criteria provided clinical testing
ISCA site 4 RCV000136079 SCV000176120 benign/likely benign See cases 2012-09-21 no assertion criteria provided clinical testing Likely benign (1), Benign (1)
ISCA site 4 RCV000139743 SCV000180336 likely benign See cases 2012-09-21 no assertion criteria provided clinical testing

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