ClinVar Miner

Variants in gene NCAM2

Minimum submission review status: Collection method:
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Gene type:
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If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic likely pathogenic uncertain significance likely benign benign total
0 0 76 12 9 97

Condition and significance breakdown #

Total conditions: 6
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Condition uncertain significance likely benign benign total
not specified 56 2 0 58
not provided 18 3 1 22
NCAM2-related disorder 0 6 7 13
See cases 2 0 0 2
Premature ovarian failure 0 0 1 1
Primary amenorrhea 0 1 0 1

Submitter and significance breakdown #

Total submitters: 11
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Submitter uncertain significance likely benign benign total
Ambry Genetics 56 2 0 58
Quest Diagnostics Nichols Institute San Juan Capistrano 16 1 0 17
PreventionGenetics, part of Exact Sciences 0 6 7 13
Labcorp Genetics (formerly Invitae), Labcorp 0 1 1 2
Bionano Laboratories 1 0 0 1
ISCA site 1 1 0 0 1
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology 1 0 0 1
Department of Biotechnology, Institute of Molecular and Cell Biology, University of Tartu 0 0 1 1
CeGaT Center for Human Genetics Tuebingen 0 1 0 1
Medical Cytogenetics and Molecular Genetics Laboratory, IRCCS Istituto Auxologico Italiano 0 1 0 1
Prenatal Diagnosis Center, Urumqi Maternal and Child Health Care Hospital 1 0 0 1

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